Transcriptomic changes under stress conditions with special reference to glutathione contents
Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic a...
Ausführliche Beschreibung
Autor*in: |
Boro, Priyanka [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2018 |
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Anmerkung: |
© Archana Sharma Foundation of Calcutta 2018 |
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Übergeordnetes Werk: |
Enthalten in: The nucleus - [New Delhi] : Springer India, 2010, 61(2018), 3 vom: 28. Nov., Seite 241-252 |
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Übergeordnetes Werk: |
volume:61 ; year:2018 ; number:3 ; day:28 ; month:11 ; pages:241-252 |
Links: |
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DOI / URN: |
10.1007/s13237-018-0256-5 |
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Katalog-ID: |
SPR03098047X |
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520 | |a Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. | ||
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10.1007/s13237-018-0256-5 doi (DE-627)SPR03098047X (SPR)s13237-018-0256-5-e DE-627 ger DE-627 rakwb eng Boro, Priyanka verfasserin aut Transcriptomic changes under stress conditions with special reference to glutathione contents 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Archana Sharma Foundation of Calcutta 2018 Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. GSH (dpeaa)DE-He213 Plant stress response (dpeaa)DE-He213 Multigenicity (dpeaa)DE-He213 Cross-talk (dpeaa)DE-He213 Sultana, Asma aut Mandal, Kajal aut Chattopadhyay, Sharmila aut Enthalten in The nucleus [New Delhi] : Springer India, 2010 61(2018), 3 vom: 28. Nov., Seite 241-252 (DE-627)644282746 (DE-600)2589081-5 0976-7975 nnns volume:61 year:2018 number:3 day:28 month:11 pages:241-252 https://dx.doi.org/10.1007/s13237-018-0256-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 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_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 61 2018 3 28 11 241-252 |
spelling |
10.1007/s13237-018-0256-5 doi (DE-627)SPR03098047X (SPR)s13237-018-0256-5-e DE-627 ger DE-627 rakwb eng Boro, Priyanka verfasserin aut Transcriptomic changes under stress conditions with special reference to glutathione contents 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Archana Sharma Foundation of Calcutta 2018 Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. GSH (dpeaa)DE-He213 Plant stress response (dpeaa)DE-He213 Multigenicity (dpeaa)DE-He213 Cross-talk (dpeaa)DE-He213 Sultana, Asma aut Mandal, Kajal aut Chattopadhyay, Sharmila aut Enthalten in The nucleus [New Delhi] : Springer India, 2010 61(2018), 3 vom: 28. Nov., Seite 241-252 (DE-627)644282746 (DE-600)2589081-5 0976-7975 nnns volume:61 year:2018 number:3 day:28 month:11 pages:241-252 https://dx.doi.org/10.1007/s13237-018-0256-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 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_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 61 2018 3 28 11 241-252 |
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10.1007/s13237-018-0256-5 doi (DE-627)SPR03098047X (SPR)s13237-018-0256-5-e DE-627 ger DE-627 rakwb eng Boro, Priyanka verfasserin aut Transcriptomic changes under stress conditions with special reference to glutathione contents 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Archana Sharma Foundation of Calcutta 2018 Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. GSH (dpeaa)DE-He213 Plant stress response (dpeaa)DE-He213 Multigenicity (dpeaa)DE-He213 Cross-talk (dpeaa)DE-He213 Sultana, Asma aut Mandal, Kajal aut Chattopadhyay, Sharmila aut Enthalten in The nucleus [New Delhi] : Springer India, 2010 61(2018), 3 vom: 28. Nov., Seite 241-252 (DE-627)644282746 (DE-600)2589081-5 0976-7975 nnns volume:61 year:2018 number:3 day:28 month:11 pages:241-252 https://dx.doi.org/10.1007/s13237-018-0256-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 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_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 61 2018 3 28 11 241-252 |
allfieldsGer |
10.1007/s13237-018-0256-5 doi (DE-627)SPR03098047X (SPR)s13237-018-0256-5-e DE-627 ger DE-627 rakwb eng Boro, Priyanka verfasserin aut Transcriptomic changes under stress conditions with special reference to glutathione contents 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Archana Sharma Foundation of Calcutta 2018 Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. GSH (dpeaa)DE-He213 Plant stress response (dpeaa)DE-He213 Multigenicity (dpeaa)DE-He213 Cross-talk (dpeaa)DE-He213 Sultana, Asma aut Mandal, Kajal aut Chattopadhyay, Sharmila aut Enthalten in The nucleus [New Delhi] : Springer India, 2010 61(2018), 3 vom: 28. Nov., Seite 241-252 (DE-627)644282746 (DE-600)2589081-5 0976-7975 nnns volume:61 year:2018 number:3 day:28 month:11 pages:241-252 https://dx.doi.org/10.1007/s13237-018-0256-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 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_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 61 2018 3 28 11 241-252 |
allfieldsSound |
10.1007/s13237-018-0256-5 doi (DE-627)SPR03098047X (SPR)s13237-018-0256-5-e DE-627 ger DE-627 rakwb eng Boro, Priyanka verfasserin aut Transcriptomic changes under stress conditions with special reference to glutathione contents 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Archana Sharma Foundation of Calcutta 2018 Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. GSH (dpeaa)DE-He213 Plant stress response (dpeaa)DE-He213 Multigenicity (dpeaa)DE-He213 Cross-talk (dpeaa)DE-He213 Sultana, Asma aut Mandal, Kajal aut Chattopadhyay, Sharmila aut Enthalten in The nucleus [New Delhi] : Springer India, 2010 61(2018), 3 vom: 28. Nov., Seite 241-252 (DE-627)644282746 (DE-600)2589081-5 0976-7975 nnns volume:61 year:2018 number:3 day:28 month:11 pages:241-252 https://dx.doi.org/10.1007/s13237-018-0256-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 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_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 61 2018 3 28 11 241-252 |
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English |
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Enthalten in The nucleus 61(2018), 3 vom: 28. Nov., Seite 241-252 volume:61 year:2018 number:3 day:28 month:11 pages:241-252 |
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Enthalten in The nucleus 61(2018), 3 vom: 28. Nov., Seite 241-252 volume:61 year:2018 number:3 day:28 month:11 pages:241-252 |
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GSH Plant stress response Multigenicity Cross-talk |
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The nucleus |
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Boro, Priyanka @@aut@@ Sultana, Asma @@aut@@ Mandal, Kajal @@aut@@ Chattopadhyay, Sharmila @@aut@@ |
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2018-11-28T00:00:00Z |
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transcriptomic changes under stress conditions with special reference to glutathione contents |
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Transcriptomic changes under stress conditions with special reference to glutathione contents |
abstract |
Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. © Archana Sharma Foundation of Calcutta 2018 |
abstractGer |
Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. © Archana Sharma Foundation of Calcutta 2018 |
abstract_unstemmed |
Abstract Plants are sessile organisms. They have to endure the environmental catastrophe throughout their life cycle. To survive in these hostile surroundings, plants posses an efficient and fine-tuned defense mechanism. This is a well established fact that various defense molecules viz. salicylic acid (SA), jasmonic acid, abscisic acid (ABA), ethylene (ET) and so on, are working in a synergistic as well as antagonistic fashion to establish and activate the effective defense mechanism. Interestingly, glutathione is gaining a gradual importance in this complex scenario. This multifunctional biomolecule exists in two forms. The reduced form, viz. GSH, is primarily present at millimolar concentrations in various plant tissues as compared to its oxidized form, glutathione disulfide, GSSG. Proteo-genomics analysis confirmed that GSH plays a vital role in plant resistance against biotic and abiotic stresses by stimulating various defense genes and proteins. In recent times, it has been reported that modulation of GSH contents transmits information through diverse signaling mechanisms. GSH also modulates various stresses and defense related genes by interacting with ABA and ET in response to abiotic stress conditions. However, there are still many unanswered questions about the intricate molecular mechanism of GSH’s contribution in plant defense. With these backgrounds, presently we primarily discussed the transcriptomic changes under stress conditions in Arabidopsis thaliana at altered GSH contents. Transcriptomic profiling of phytoalexin-deficient mutant (pad2.1), a GSH depleted A. thaliana mutant, in response to combined cold and osmotic stress treatment, was compared to that of A. thaliana ecotype Col-0, the wild type, with a view to identify the genes altered under changed GSH conditions to combat stress. It was evident from these datasets that the transcript level responses of pad2.1 to this treatment were massive. Again, analysis of combined cold and osmotic stress treated other mutants of Arabidopsis transcriptome was performed to elucidate the crosstalk between the ABA, ET and GSH. Results revealed the differential regulation of about 2313 and 4131 transcripts in A. thaliana mutants viz. ethylene insensitive (ein2) and ABA deficient 1(aba1.6) respectively. Together, present findings elucidate an active interplay of GSH with SA, ET, and ABA to combat environmental stress conditions in planta. © Archana Sharma Foundation of Calcutta 2018 |
collection_details |
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3 |
title_short |
Transcriptomic changes under stress conditions with special reference to glutathione contents |
url |
https://dx.doi.org/10.1007/s13237-018-0256-5 |
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author2 |
Sultana, Asma Mandal, Kajal Chattopadhyay, Sharmila |
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doi_str |
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up_date |
2024-07-03T21:17:39.785Z |
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score |
7.399419 |