The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression
<p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum...
Ausführliche Beschreibung
Autor*in: |
Merino Fuencisla [verfasserIn] Novo-Uzal Esther [verfasserIn] Pomar Federico [verfasserIn] Gayoso Carmen [verfasserIn] Martínez de Ilárduya Óskar [verfasserIn] |
---|
Format: |
E-Artikel |
---|---|
Sprache: |
Englisch |
Erschienen: |
2010 |
---|
Übergeordnetes Werk: |
In: BMC Plant Biology - BMC, 2003, 10(2010), 1, p 232 |
---|---|
Übergeordnetes Werk: |
volume:10 ; year:2010 ; number:1, p 232 |
Links: |
---|
DOI / URN: |
10.1186/1471-2229-10-232 |
---|
Katalog-ID: |
DOAJ058857540 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | DOAJ058857540 | ||
003 | DE-627 | ||
005 | 20230503064222.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230228s2010 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1186/1471-2229-10-232 |2 doi | |
035 | |a (DE-627)DOAJ058857540 | ||
035 | |a (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
050 | 0 | |a QK1-989 | |
100 | 0 | |a Merino Fuencisla |e verfasserin |4 aut | |
245 | 1 | 4 | |a The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
264 | 1 | |c 2010 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a <p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< | ||
653 | 0 | |a Botany | |
700 | 0 | |a Novo-Uzal Esther |e verfasserin |4 aut | |
700 | 0 | |a Pomar Federico |e verfasserin |4 aut | |
700 | 0 | |a Gayoso Carmen |e verfasserin |4 aut | |
700 | 0 | |a Martínez de Ilárduya Óskar |e verfasserin |4 aut | |
773 | 0 | 8 | |i In |t BMC Plant Biology |d BMC, 2003 |g 10(2010), 1, p 232 |w (DE-627)335489060 |w (DE-600)2059868-3 |x 14712229 |7 nnns |
773 | 1 | 8 | |g volume:10 |g year:2010 |g number:1, p 232 |
856 | 4 | 0 | |u https://doi.org/10.1186/1471-2229-10-232 |z kostenfrei |
856 | 4 | 0 | |u https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 |z kostenfrei |
856 | 4 | 0 | |u http://www.biomedcentral.com/1471-2229/10/232 |z kostenfrei |
856 | 4 | 2 | |u https://doaj.org/toc/1471-2229 |y Journal toc |z kostenfrei |
912 | |a GBV_USEFLAG_A | ||
912 | |a SYSFLAG_A | ||
912 | |a GBV_DOAJ | ||
912 | |a SSG-OLC-PHA | ||
912 | |a GBV_ILN_11 | ||
912 | |a GBV_ILN_20 | ||
912 | |a GBV_ILN_22 | ||
912 | |a GBV_ILN_23 | ||
912 | |a GBV_ILN_24 | ||
912 | |a GBV_ILN_39 | ||
912 | |a GBV_ILN_40 | ||
912 | |a GBV_ILN_60 | ||
912 | |a GBV_ILN_62 | ||
912 | |a GBV_ILN_63 | ||
912 | |a GBV_ILN_65 | ||
912 | |a GBV_ILN_69 | ||
912 | |a GBV_ILN_70 | ||
912 | |a GBV_ILN_73 | ||
912 | |a GBV_ILN_74 | ||
912 | |a GBV_ILN_95 | ||
912 | |a GBV_ILN_105 | ||
912 | |a GBV_ILN_110 | ||
912 | |a GBV_ILN_151 | ||
912 | |a GBV_ILN_161 | ||
912 | |a GBV_ILN_170 | ||
912 | |a GBV_ILN_206 | ||
912 | |a GBV_ILN_213 | ||
912 | |a GBV_ILN_224 | ||
912 | |a GBV_ILN_230 | ||
912 | |a GBV_ILN_285 | ||
912 | |a GBV_ILN_293 | ||
912 | |a GBV_ILN_602 | ||
912 | |a GBV_ILN_702 | ||
912 | |a GBV_ILN_2001 | ||
912 | |a GBV_ILN_2003 | ||
912 | |a GBV_ILN_2005 | ||
912 | |a GBV_ILN_2006 | ||
912 | |a GBV_ILN_2008 | ||
912 | |a GBV_ILN_2009 | ||
912 | |a GBV_ILN_2010 | ||
912 | |a GBV_ILN_2011 | ||
912 | |a GBV_ILN_2014 | ||
912 | |a GBV_ILN_2015 | ||
912 | |a GBV_ILN_2020 | ||
912 | |a GBV_ILN_2021 | ||
912 | |a GBV_ILN_2025 | ||
912 | |a GBV_ILN_2031 | ||
912 | |a GBV_ILN_2038 | ||
912 | |a GBV_ILN_2044 | ||
912 | |a GBV_ILN_2048 | ||
912 | |a GBV_ILN_2050 | ||
912 | |a GBV_ILN_2055 | ||
912 | |a GBV_ILN_2056 | ||
912 | |a GBV_ILN_2057 | ||
912 | |a GBV_ILN_2061 | ||
912 | |a GBV_ILN_2111 | ||
912 | |a GBV_ILN_2113 | ||
912 | |a GBV_ILN_2190 | ||
912 | |a GBV_ILN_4012 | ||
912 | |a GBV_ILN_4037 | ||
912 | |a GBV_ILN_4112 | ||
912 | |a GBV_ILN_4125 | ||
912 | |a GBV_ILN_4126 | ||
912 | |a GBV_ILN_4249 | ||
912 | |a GBV_ILN_4305 | ||
912 | |a GBV_ILN_4306 | ||
912 | |a GBV_ILN_4307 | ||
912 | |a GBV_ILN_4313 | ||
912 | |a GBV_ILN_4322 | ||
912 | |a GBV_ILN_4323 | ||
912 | |a GBV_ILN_4324 | ||
912 | |a GBV_ILN_4325 | ||
912 | |a GBV_ILN_4338 | ||
912 | |a GBV_ILN_4367 | ||
912 | |a GBV_ILN_4700 | ||
951 | |a AR | ||
952 | |d 10 |j 2010 |e 1, p 232 |
author_variant |
m f mf n u e nue p f pf g c gc m d i ó mdió |
---|---|
matchkey_str |
article:14712229:2010----::hivimdaerssacrsosoteoaootetclimalaiivlehu2uou2uprxdsad |
hierarchy_sort_str |
2010 |
callnumber-subject-code |
QK |
publishDate |
2010 |
allfields |
10.1186/1471-2229-10-232 doi (DE-627)DOAJ058857540 (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 DE-627 ger DE-627 rakwb eng QK1-989 Merino Fuencisla verfasserin aut The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< Botany Novo-Uzal Esther verfasserin aut Pomar Federico verfasserin aut Gayoso Carmen verfasserin aut Martínez de Ilárduya Óskar verfasserin aut In BMC Plant Biology BMC, 2003 10(2010), 1, p 232 (DE-627)335489060 (DE-600)2059868-3 14712229 nnns volume:10 year:2010 number:1, p 232 https://doi.org/10.1186/1471-2229-10-232 kostenfrei https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 kostenfrei http://www.biomedcentral.com/1471-2229/10/232 kostenfrei https://doaj.org/toc/1471-2229 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2010 1, p 232 |
spelling |
10.1186/1471-2229-10-232 doi (DE-627)DOAJ058857540 (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 DE-627 ger DE-627 rakwb eng QK1-989 Merino Fuencisla verfasserin aut The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< Botany Novo-Uzal Esther verfasserin aut Pomar Federico verfasserin aut Gayoso Carmen verfasserin aut Martínez de Ilárduya Óskar verfasserin aut In BMC Plant Biology BMC, 2003 10(2010), 1, p 232 (DE-627)335489060 (DE-600)2059868-3 14712229 nnns volume:10 year:2010 number:1, p 232 https://doi.org/10.1186/1471-2229-10-232 kostenfrei https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 kostenfrei http://www.biomedcentral.com/1471-2229/10/232 kostenfrei https://doaj.org/toc/1471-2229 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2010 1, p 232 |
allfields_unstemmed |
10.1186/1471-2229-10-232 doi (DE-627)DOAJ058857540 (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 DE-627 ger DE-627 rakwb eng QK1-989 Merino Fuencisla verfasserin aut The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< Botany Novo-Uzal Esther verfasserin aut Pomar Federico verfasserin aut Gayoso Carmen verfasserin aut Martínez de Ilárduya Óskar verfasserin aut In BMC Plant Biology BMC, 2003 10(2010), 1, p 232 (DE-627)335489060 (DE-600)2059868-3 14712229 nnns volume:10 year:2010 number:1, p 232 https://doi.org/10.1186/1471-2229-10-232 kostenfrei https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 kostenfrei http://www.biomedcentral.com/1471-2229/10/232 kostenfrei https://doaj.org/toc/1471-2229 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2010 1, p 232 |
allfieldsGer |
10.1186/1471-2229-10-232 doi (DE-627)DOAJ058857540 (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 DE-627 ger DE-627 rakwb eng QK1-989 Merino Fuencisla verfasserin aut The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< Botany Novo-Uzal Esther verfasserin aut Pomar Federico verfasserin aut Gayoso Carmen verfasserin aut Martínez de Ilárduya Óskar verfasserin aut In BMC Plant Biology BMC, 2003 10(2010), 1, p 232 (DE-627)335489060 (DE-600)2059868-3 14712229 nnns volume:10 year:2010 number:1, p 232 https://doi.org/10.1186/1471-2229-10-232 kostenfrei https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 kostenfrei http://www.biomedcentral.com/1471-2229/10/232 kostenfrei https://doaj.org/toc/1471-2229 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2010 1, p 232 |
allfieldsSound |
10.1186/1471-2229-10-232 doi (DE-627)DOAJ058857540 (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 DE-627 ger DE-627 rakwb eng QK1-989 Merino Fuencisla verfasserin aut The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< Botany Novo-Uzal Esther verfasserin aut Pomar Federico verfasserin aut Gayoso Carmen verfasserin aut Martínez de Ilárduya Óskar verfasserin aut In BMC Plant Biology BMC, 2003 10(2010), 1, p 232 (DE-627)335489060 (DE-600)2059868-3 14712229 nnns volume:10 year:2010 number:1, p 232 https://doi.org/10.1186/1471-2229-10-232 kostenfrei https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 kostenfrei http://www.biomedcentral.com/1471-2229/10/232 kostenfrei https://doaj.org/toc/1471-2229 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2010 1, p 232 |
language |
English |
source |
In BMC Plant Biology 10(2010), 1, p 232 volume:10 year:2010 number:1, p 232 |
sourceStr |
In BMC Plant Biology 10(2010), 1, p 232 volume:10 year:2010 number:1, p 232 |
format_phy_str_mv |
Article |
institution |
findex.gbv.de |
topic_facet |
Botany |
isfreeaccess_bool |
true |
container_title |
BMC Plant Biology |
authorswithroles_txt_mv |
Merino Fuencisla @@aut@@ Novo-Uzal Esther @@aut@@ Pomar Federico @@aut@@ Gayoso Carmen @@aut@@ Martínez de Ilárduya Óskar @@aut@@ |
publishDateDaySort_date |
2010-01-01T00:00:00Z |
hierarchy_top_id |
335489060 |
id |
DOAJ058857540 |
language_de |
englisch |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ058857540</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503064222.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230228s2010 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1186/1471-2229-10-232</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ058857540</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ2dcf793f68194eaeb6700791696dac34</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QK1-989</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Merino Fuencisla</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="4"><subfield code="a">The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2010</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a"><p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p<</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Botany</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Novo-Uzal Esther</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Pomar Federico</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Gayoso Carmen</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Martínez de Ilárduya Óskar</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">BMC Plant Biology</subfield><subfield code="d">BMC, 2003</subfield><subfield code="g">10(2010), 1, p 232</subfield><subfield code="w">(DE-627)335489060</subfield><subfield code="w">(DE-600)2059868-3</subfield><subfield code="x">14712229</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:10</subfield><subfield code="g">year:2010</subfield><subfield code="g">number:1, p 232</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1186/1471-2229-10-232</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/2dcf793f68194eaeb6700791696dac34</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.biomedcentral.com/1471-2229/10/232</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/1471-2229</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_11</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_170</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_206</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_702</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2001</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2003</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2005</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2006</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2008</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2009</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2010</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2011</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2015</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2020</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2025</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2031</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2038</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2044</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2048</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2050</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2055</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2056</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2057</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2061</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2111</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2113</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2190</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">10</subfield><subfield code="j">2010</subfield><subfield code="e">1, p 232</subfield></datafield></record></collection>
|
callnumber-first |
Q - Science |
author |
Merino Fuencisla |
spellingShingle |
Merino Fuencisla misc QK1-989 misc Botany The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
authorStr |
Merino Fuencisla |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)335489060 |
format |
electronic Article |
delete_txt_mv |
keep |
author_role |
aut aut aut aut aut |
collection |
DOAJ |
remote_str |
true |
callnumber-label |
QK1-989 |
illustrated |
Not Illustrated |
issn |
14712229 |
topic_title |
QK1-989 The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
topic |
misc QK1-989 misc Botany |
topic_unstemmed |
misc QK1-989 misc Botany |
topic_browse |
misc QK1-989 misc Botany |
format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
format_main_str_mv |
Text Zeitschrift/Artikel |
carriertype_str_mv |
cr |
hierarchy_parent_title |
BMC Plant Biology |
hierarchy_parent_id |
335489060 |
hierarchy_top_title |
BMC Plant Biology |
isfreeaccess_txt |
true |
familylinks_str_mv |
(DE-627)335489060 (DE-600)2059868-3 |
title |
The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
ctrlnum |
(DE-627)DOAJ058857540 (DE-599)DOAJ2dcf793f68194eaeb6700791696dac34 |
title_full |
The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
author_sort |
Merino Fuencisla |
journal |
BMC Plant Biology |
journalStr |
BMC Plant Biology |
callnumber-first-code |
Q |
lang_code |
eng |
isOA_bool |
true |
recordtype |
marc |
publishDateSort |
2010 |
contenttype_str_mv |
txt |
author_browse |
Merino Fuencisla Novo-Uzal Esther Pomar Federico Gayoso Carmen Martínez de Ilárduya Óskar |
container_volume |
10 |
class |
QK1-989 |
format_se |
Elektronische Aufsätze |
author-letter |
Merino Fuencisla |
doi_str_mv |
10.1186/1471-2229-10-232 |
author2-role |
verfasserin |
title_sort |
<it<ve</it<-mediated resistance response of the tomato to <it<verticillium dahliae </it<involves h<sub<2</sub<o<sub<2</sub<, peroxidase and lignins and drives <it<pal </it<gene expression |
callnumber |
QK1-989 |
title_auth |
The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
abstract |
<p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< |
abstractGer |
<p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< |
abstract_unstemmed |
<p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p< |
collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 |
container_issue |
1, p 232 |
title_short |
The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression |
url |
https://doi.org/10.1186/1471-2229-10-232 https://doaj.org/article/2dcf793f68194eaeb6700791696dac34 http://www.biomedcentral.com/1471-2229/10/232 https://doaj.org/toc/1471-2229 |
remote_bool |
true |
author2 |
Novo-Uzal Esther Pomar Federico Gayoso Carmen Martínez de Ilárduya Óskar |
author2Str |
Novo-Uzal Esther Pomar Federico Gayoso Carmen Martínez de Ilárduya Óskar |
ppnlink |
335489060 |
callnumber-subject |
QK - Botany |
mediatype_str_mv |
c |
isOA_txt |
true |
hochschulschrift_bool |
false |
doi_str |
10.1186/1471-2229-10-232 |
callnumber-a |
QK1-989 |
up_date |
2024-07-03T20:27:43.178Z |
_version_ |
1803591051577917440 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ058857540</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503064222.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230228s2010 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1186/1471-2229-10-232</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ058857540</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ2dcf793f68194eaeb6700791696dac34</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QK1-989</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Merino Fuencisla</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="4"><subfield code="a">The <it<Ve</it<-mediated resistance response of the tomato to <it<Verticillium dahliae </it<involves H<sub<2</sub<O<sub<2</sub<, peroxidase and lignins and drives <it<PAL </it<gene expression</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2010</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a"><p<Abstract</p< <p<Background</p< <p<<it<Verticillium dahliae </it<is a fungal pathogen that infects a wide range of hosts. The only known genes for resistance to <it<Verticillium </it<in the Solanaceae are found in the tomato (<it<Solanum lycopersicum</it<) <it<Ve </it<locus, formed by two linked genes, <it<Ve1 </it<and <it<Ve2</it<. To characterize the resistance response mediated by the tomato <it<Ve </it<gene, we inoculated two nearly isogenic tomato lines, LA3030 (<it<ve</it</<it<ve</it<) and LA3038 (<it<Ve</it</<it<Ve</it<), with <it<V. dahliae</it<.</p< <p<Results</p< <p<We found induction of H<sub<2</sub<O<sub<2 </sub<production in roots of inoculated plants, followed by an increase in peroxidase activity only in roots of inoculated resistant plants. Phenylalanine-ammonia lyase (PAL) activity was also increased in resistant roots 2 hours after inoculation, while induction of PAL activity in susceptible roots was not seen until 48 hours after inoculation. Phenylpropanoid metabolism was also affected, with increases in ferulic acid, <it<p</it<-coumaric acid, vanillin and <it<p</it<-hydroxybenzaldehyde contents in resistant roots after inoculation. Six tomato <it<PAL </it<cDNA sequences (<it<PAL1 </it<- <it<PAL6</it<) were found in the SolGenes tomato EST database. RT-PCR analysis showed that these genes were expressed in all organs of the plant, albeit at different levels. Real-time RT-PCR indicated distinct patterns of expression of the different <it<PAL </it<genes in <it<V. dahliae</it<-inoculated roots. Phylogenetic analysis of 48 partial <it<PAL </it<cDNAs corresponding to 19 plant species grouped angiosperm <it<PAL </it<sequences into four clusters, suggesting functional differences among the six tomato genes, with <it<PAL2 </it<and <it<PAL6 </it<presumably involved in lignification, and the remaining <it<PAL </it<genes implicated in other biological processes.</p< <p<An increase in the synthesis of lignins was found 16 and 28 days after inoculation in both lines; this increase was greater and faster to develop in the resistant line. In both resistant and susceptible inoculated plants, an increase in the ratio of guaiacyl/syringyl units was detected 16 days after inoculation, resulting from the lowered amount of syringyl units in the lignins of inoculated plants.</p< <p<Conclusions</p< <p<The interaction between the tomato and <it<V. dahliae </it<triggered a number of short- and long-term defensive mechanisms. Differences were found between compatible and incompatible interactions, including onset of H<sub<2</sub<O<sub<2 </sub<production and activities of peroxidase and PAL, and phenylpropanoid metabolism and synthesis of lignins.</p<</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Botany</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Novo-Uzal Esther</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Pomar Federico</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Gayoso Carmen</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Martínez de Ilárduya Óskar</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">BMC Plant Biology</subfield><subfield code="d">BMC, 2003</subfield><subfield code="g">10(2010), 1, p 232</subfield><subfield code="w">(DE-627)335489060</subfield><subfield code="w">(DE-600)2059868-3</subfield><subfield code="x">14712229</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:10</subfield><subfield code="g">year:2010</subfield><subfield code="g">number:1, p 232</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1186/1471-2229-10-232</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/2dcf793f68194eaeb6700791696dac34</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.biomedcentral.com/1471-2229/10/232</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/1471-2229</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_11</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_170</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_206</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_702</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2001</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2003</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2005</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2006</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2008</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2009</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2010</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2011</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2015</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2020</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2025</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2031</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2038</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2044</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2048</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2050</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2055</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2056</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2057</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2061</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2111</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2113</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2190</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">10</subfield><subfield code="j">2010</subfield><subfield code="e">1, p 232</subfield></datafield></record></collection>
|
score |
7.400522 |