One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana
Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the m...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Shumin, Zhou [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2015 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer-Verlag Berlin Heidelberg 2015 |
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| Übergeordnetes Werk: |
Enthalten in: Plant cell reports - Berlin : Springer, 1981, 34(2015), 10 vom: 02. Juli, Seite 1773-1780 |
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| Übergeordnetes Werk: |
volume:34 ; year:2015 ; number:10 ; day:02 ; month:07 ; pages:1773-1780 |
| Links: |
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| DOI / URN: |
10.1007/s00299-015-1823-8 |
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| Katalog-ID: |
SPR003907538 |
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| 100 | 1 | |a Shumin, Zhou |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana |
| 264 | 1 | |c 2015 | |
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| 520 | |a Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. | ||
| 650 | 4 | |a Tapetum |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a -element |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a CTCC |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a GCTGG |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Yan, Chen |4 aut | |
| 700 | 1 | |a Hulin, Sun |4 aut | |
| 700 | 1 | |a Bang, Zheng |4 aut | |
| 700 | 1 | |a Licheng, Sun |4 aut | |
| 700 | 1 | |a Wei, Zhang |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Plant cell reports |d Berlin : Springer, 1981 |g 34(2015), 10 vom: 02. Juli, Seite 1773-1780 |w (DE-627)254630367 |w (DE-600)1462082-0 |x 1432-203X |7 nnns |
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| 912 | |a GBV_ILN_100 | ||
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| 912 | |a GBV_ILN_105 | ||
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| 912 | |a GBV_ILN_2011 | ||
| 912 | |a GBV_ILN_2014 | ||
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| 912 | |a GBV_ILN_2021 | ||
| 912 | |a GBV_ILN_2025 | ||
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| 912 | |a GBV_ILN_2027 | ||
| 912 | |a GBV_ILN_2031 | ||
| 912 | |a GBV_ILN_2034 | ||
| 912 | |a GBV_ILN_2037 | ||
| 912 | |a GBV_ILN_2038 | ||
| 912 | |a GBV_ILN_2039 | ||
| 912 | |a GBV_ILN_2044 | ||
| 912 | |a GBV_ILN_2048 | ||
| 912 | |a GBV_ILN_2049 | ||
| 912 | |a GBV_ILN_2050 | ||
| 912 | |a GBV_ILN_2055 | ||
| 912 | |a GBV_ILN_2057 | ||
| 912 | |a GBV_ILN_2059 | ||
| 912 | |a GBV_ILN_2061 | ||
| 912 | |a GBV_ILN_2064 | ||
| 912 | |a GBV_ILN_2065 | ||
| 912 | |a GBV_ILN_2068 | ||
| 912 | |a GBV_ILN_2070 | ||
| 912 | |a GBV_ILN_2086 | ||
| 912 | |a GBV_ILN_2088 | ||
| 912 | |a GBV_ILN_2093 | ||
| 912 | |a GBV_ILN_2106 | ||
| 912 | |a GBV_ILN_2107 | ||
| 912 | |a GBV_ILN_2108 | ||
| 912 | |a GBV_ILN_2110 | ||
| 912 | |a GBV_ILN_2111 | ||
| 912 | |a GBV_ILN_2112 | ||
| 912 | |a GBV_ILN_2113 | ||
| 912 | |a GBV_ILN_2116 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2119 | ||
| 912 | |a GBV_ILN_2122 | ||
| 912 | |a GBV_ILN_2129 | ||
| 912 | |a GBV_ILN_2143 | ||
| 912 | |a GBV_ILN_2144 | ||
| 912 | |a GBV_ILN_2147 | ||
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| 912 | |a GBV_ILN_2152 | ||
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| 912 | |a GBV_ILN_2188 | ||
| 912 | |a GBV_ILN_2190 | ||
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| 912 | |a GBV_ILN_2336 | ||
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| 912 | |a GBV_ILN_4037 | ||
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| 912 | |a GBV_ILN_4112 | ||
| 912 | |a GBV_ILN_4125 | ||
| 912 | |a GBV_ILN_4126 | ||
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| 912 | |a GBV_ILN_4246 | ||
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| 912 | |a GBV_ILN_4251 | ||
| 912 | |a GBV_ILN_4305 | ||
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| 912 | |a GBV_ILN_4307 | ||
| 912 | |a GBV_ILN_4313 | ||
| 912 | |a GBV_ILN_4322 | ||
| 912 | |a GBV_ILN_4323 | ||
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| 912 | |a GBV_ILN_4326 | ||
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10.1007/s00299-015-1823-8 doi (DE-627)SPR003907538 (SPR)s00299-015-1823-8-e DE-627 ger DE-627 rakwb eng Shumin, Zhou verfasserin aut One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. Tapetum (dpeaa)DE-He213 -element (dpeaa)DE-He213 CTCC (dpeaa)DE-He213 GCTGG (dpeaa)DE-He213 Yan, Chen aut Hulin, Sun aut Bang, Zheng aut Licheng, Sun aut Wei, Zhang aut Enthalten in Plant cell reports Berlin : Springer, 1981 34(2015), 10 vom: 02. Juli, Seite 1773-1780 (DE-627)254630367 (DE-600)1462082-0 1432-203X nnns volume:34 year:2015 number:10 day:02 month:07 pages:1773-1780 https://dx.doi.org/10.1007/s00299-015-1823-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_152 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2190 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 10 02 07 1773-1780 |
| spelling |
10.1007/s00299-015-1823-8 doi (DE-627)SPR003907538 (SPR)s00299-015-1823-8-e DE-627 ger DE-627 rakwb eng Shumin, Zhou verfasserin aut One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. Tapetum (dpeaa)DE-He213 -element (dpeaa)DE-He213 CTCC (dpeaa)DE-He213 GCTGG (dpeaa)DE-He213 Yan, Chen aut Hulin, Sun aut Bang, Zheng aut Licheng, Sun aut Wei, Zhang aut Enthalten in Plant cell reports Berlin : Springer, 1981 34(2015), 10 vom: 02. Juli, Seite 1773-1780 (DE-627)254630367 (DE-600)1462082-0 1432-203X nnns volume:34 year:2015 number:10 day:02 month:07 pages:1773-1780 https://dx.doi.org/10.1007/s00299-015-1823-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_152 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2190 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 10 02 07 1773-1780 |
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10.1007/s00299-015-1823-8 doi (DE-627)SPR003907538 (SPR)s00299-015-1823-8-e DE-627 ger DE-627 rakwb eng Shumin, Zhou verfasserin aut One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. Tapetum (dpeaa)DE-He213 -element (dpeaa)DE-He213 CTCC (dpeaa)DE-He213 GCTGG (dpeaa)DE-He213 Yan, Chen aut Hulin, Sun aut Bang, Zheng aut Licheng, Sun aut Wei, Zhang aut Enthalten in Plant cell reports Berlin : Springer, 1981 34(2015), 10 vom: 02. Juli, Seite 1773-1780 (DE-627)254630367 (DE-600)1462082-0 1432-203X nnns volume:34 year:2015 number:10 day:02 month:07 pages:1773-1780 https://dx.doi.org/10.1007/s00299-015-1823-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_152 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2190 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 10 02 07 1773-1780 |
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10.1007/s00299-015-1823-8 doi (DE-627)SPR003907538 (SPR)s00299-015-1823-8-e DE-627 ger DE-627 rakwb eng Shumin, Zhou verfasserin aut One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. Tapetum (dpeaa)DE-He213 -element (dpeaa)DE-He213 CTCC (dpeaa)DE-He213 GCTGG (dpeaa)DE-He213 Yan, Chen aut Hulin, Sun aut Bang, Zheng aut Licheng, Sun aut Wei, Zhang aut Enthalten in Plant cell reports Berlin : Springer, 1981 34(2015), 10 vom: 02. Juli, Seite 1773-1780 (DE-627)254630367 (DE-600)1462082-0 1432-203X nnns volume:34 year:2015 number:10 day:02 month:07 pages:1773-1780 https://dx.doi.org/10.1007/s00299-015-1823-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_152 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2190 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 10 02 07 1773-1780 |
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10.1007/s00299-015-1823-8 doi (DE-627)SPR003907538 (SPR)s00299-015-1823-8-e DE-627 ger DE-627 rakwb eng Shumin, Zhou verfasserin aut One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. Tapetum (dpeaa)DE-He213 -element (dpeaa)DE-He213 CTCC (dpeaa)DE-He213 GCTGG (dpeaa)DE-He213 Yan, Chen aut Hulin, Sun aut Bang, Zheng aut Licheng, Sun aut Wei, Zhang aut Enthalten in Plant cell reports Berlin : Springer, 1981 34(2015), 10 vom: 02. Juli, Seite 1773-1780 (DE-627)254630367 (DE-600)1462082-0 1432-203X nnns volume:34 year:2015 number:10 day:02 month:07 pages:1773-1780 https://dx.doi.org/10.1007/s00299-015-1823-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_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_152 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2190 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_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 10 02 07 1773-1780 |
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Shumin, Zhou @@aut@@ Yan, Chen @@aut@@ Hulin, Sun @@aut@@ Bang, Zheng @@aut@@ Licheng, Sun @@aut@@ Wei, Zhang @@aut@@ |
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Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. 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Shumin, Zhou |
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Shumin, Zhou misc Tapetum misc -element misc CTCC misc GCTGG One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana |
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One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana Tapetum (dpeaa)DE-He213 -element (dpeaa)DE-He213 CTCC (dpeaa)DE-He213 GCTGG (dpeaa)DE-He213 |
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misc Tapetum misc -element misc CTCC misc GCTGG |
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One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana |
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One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana |
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Shumin, Zhou Yan, Chen Hulin, Sun Bang, Zheng Licheng, Sun Wei, Zhang |
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one novel cis-element is essential for correct dysfunctional tapetum 1 (dyt1) expression in arabidopsis thaliana |
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One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana |
| abstract |
Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. © Springer-Verlag Berlin Heidelberg 2015 |
| abstractGer |
Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. © Springer-Verlag Berlin Heidelberg 2015 |
| abstract_unstemmed |
Key message We studied the function ofDYT1promoter, found the important sectorscontrollingspecific expression ofDYT1, and identified a newcis-elementfor further investigation ofDYT1upstream genes. Abstract DYT1 is a core regulatory gene for tapetum development in Arabidopsis thaliana. However, the mechanism leading to DYT1 tapetum-preferential expression is still unknown up to date. Here we employed promoter truncation and deletion assay to identify a ‘CTCC’ cis-element, which was essential for correct DYT1 expression within DYT1 promoter region. Through comparing truncated DYT1 promoter-driven GFP expression, the −481 to −513 bp region from the start point of transcription (SPT) of DYT1 was found indispensable for proper DYT1 expression. Further deletion assay around this region revealed that an approximate −468 bp ‘CTCC’ sequence deletion abolished normal DYT1 expression completely. Bioinformatics assay suggested that this ‘CTCC’ motif was potentially a novel DNA-recognition sequence, providing new clue for investigating relationship between DYT1 and its upstream genes. © Springer-Verlag Berlin Heidelberg 2015 |
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One novel cis-element is essential for correct DYSFUNCTIONAL TAPETUM 1 (DYT1) expression in Arabidopsis thaliana |
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https://dx.doi.org/10.1007/s00299-015-1823-8 |
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Yan, Chen Hulin, Sun Bang, Zheng Licheng, Sun Wei, Zhang |
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2024-07-03T22:26:47.289Z |
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| score |
7.4010143 |