马铃薯StCOL基因启动子的克隆及序列分析
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- 论文作者：郭建林 ; 杨清
- 年：2017
- 作者机构：南京农业大学生命科学学院;
- 论文关键词：马铃薯 ; StCOL基因 ; 克隆 ; 序列
- 会议召开时间：2017-06-18
- 会议录名称：马铃薯产业与精准扶贫2017
- 语种：中文
- 分类号：S532
- 学会代码：ZMLS
- 会议名称：2017年马铃薯大会
- 会议地点：中国贵州毕节
- 主办单位：中国作物学会马铃薯专业委员会
- 学会名称：中国作物学会马铃薯专业委员会
- 页数：5
- 文件大小：1818k
- 原文格式：D
- 会议级别：全国
摘要
为了更好地了解StCOL基因的表达调控方式,利用技术,从马铃薯(Solanum tuberosumL.)基因组中克隆了约900bp的StCOL基因的启动子序列。序列分析显示,该启动子中存在多个光调节元件及非生物胁迫反应元件,如GATA-box、I-box、MYC识别位点和MYB结合位点等。
引文
[1]Martinez-Garcia J F,Virgos-Soler A,Prat S.Control of photoperiod-regulated tuberization in potato by the Arabidopsisflowering-time gene CONSTANS[J].Proceedings of the National Academy of Sciences,2002,99(23):15 211-15 216.
[2]Abe H,Urao T,Ito T,et al.Arabidopsis At MYC2(b HLH)and At MYB2(MYB)function as transcriptional activators inabscisic acid signaling[J].Plant and Cell Physiology,2003(15):63-78.
[3]Tyagi A K.Plant genes and their expression[J].Current Science,2001,80(2):161-169.
[4]闫新甫.转基因植物[M].北京:科学出版社,2002.
[5]Nakamura M,Tsunoda T,Obokata J.Photosynthesis nuclear genes generally lack TATA-boxes:A tobacco photosystem I gene responds to light through an initiater[J].Plant Journal,2002,29:1-10.
[6]Degenhardt J,Tobin E M.A DNA binding activity for one of two closely defined phytochrome regulatory elements in anLhcb promoter is more abundant in etiolated than in green plants[J].Plant Cell,1996,8(1):31-41.
[7]Borello U,Caccarelli E,Giuliano G.Constitutive,light-responsive and circadian clock-responsive factors compete forthe different I box elements in plant light-regulated promoters[J].Plant Journal for Cell and Molecular Biology,1993(4):611-619.
[8]Doyle M R,Davis S J,Bastow R M,et al.The ELF4 gene controls circadian rhythms and flowering time in Arabidopsisthaliana[J].Nature,2002,419(6902):74-77.
[9]Grotewold E,Drummond B J,Bowen B,et al.The myb-homologous P gene controls phlobaphene pigmentation in maizefloral organs by directly activating a flavonoid biosynthetic gene subset[J].Cell,1994,76(3):543-553.
[10]Reyes J C,Muro-Pastor M I,Florencio F J.The GATA family of transcription factors in Arabidopsis and rice[J].PlantPhysiology,2004,134(4):1 718-1 732.
[11]Saghaimaroof M A,Soliman K M,Jorgensen R A,et al.Ribosomal DNA spacer length polymorphisms in barley:Men-delian inheritance,chromosomal location and population dynamics[J].Proceedings of the National Academy of Sciences ofthe United States of America,1984,81(24):8 014-8 018.
[12]Singh K B.Transcriptional regulation in plants:The importance of combinatorial control[J].Plant Physiology,1998,118(4):1 111-1 120.
[13]Thum K E,Kim M,Morishige D T,et al.Analysis of barley chloroplast psb D light-responsive promoter elements intransplastomic tobacco[J].Plant Molecular Biology,2001,47(3):353-366.
[14]Xu N,Hagen G,Guilfoyle T.Multiple auxin response modules in the soybean SAUR15A promoter[J].Plant Science,1997,126(2):193-201.
[15]Xue G P.The DNA-binding activity of an AP2 transcriptional activator Hv CBF2 involved in regulation of low-temperatureresponsive genes in barley is modulated by temperature[J].Plant Journal,2003,33(2):373-383.
[16]Yanagisawa S,Schmidt R J.Diversity and similarity among recognition sequences of Dof transcription factors[J].PlantJournal,1999,17(2):209-214.
[2]Abe H,Urao T,Ito T,et al.Arabidopsis At MYC2(b HLH)and At MYB2(MYB)function as transcriptional activators inabscisic acid signaling[J].Plant and Cell Physiology,2003(15):63-78.
[3]Tyagi A K.Plant genes and their expression[J].Current Science,2001,80(2):161-169.
[4]闫新甫.转基因植物[M].北京:科学出版社,2002.
[5]Nakamura M,Tsunoda T,Obokata J.Photosynthesis nuclear genes generally lack TATA-boxes:A tobacco photosystem I gene responds to light through an initiater[J].Plant Journal,2002,29:1-10.
[6]Degenhardt J,Tobin E M.A DNA binding activity for one of two closely defined phytochrome regulatory elements in anLhcb promoter is more abundant in etiolated than in green plants[J].Plant Cell,1996,8(1):31-41.
[7]Borello U,Caccarelli E,Giuliano G.Constitutive,light-responsive and circadian clock-responsive factors compete forthe different I box elements in plant light-regulated promoters[J].Plant Journal for Cell and Molecular Biology,1993(4):611-619.
[8]Doyle M R,Davis S J,Bastow R M,et al.The ELF4 gene controls circadian rhythms and flowering time in Arabidopsisthaliana[J].Nature,2002,419(6902):74-77.
[9]Grotewold E,Drummond B J,Bowen B,et al.The myb-homologous P gene controls phlobaphene pigmentation in maizefloral organs by directly activating a flavonoid biosynthetic gene subset[J].Cell,1994,76(3):543-553.
[10]Reyes J C,Muro-Pastor M I,Florencio F J.The GATA family of transcription factors in Arabidopsis and rice[J].PlantPhysiology,2004,134(4):1 718-1 732.
[11]Saghaimaroof M A,Soliman K M,Jorgensen R A,et al.Ribosomal DNA spacer length polymorphisms in barley:Men-delian inheritance,chromosomal location and population dynamics[J].Proceedings of the National Academy of Sciences ofthe United States of America,1984,81(24):8 014-8 018.
[12]Singh K B.Transcriptional regulation in plants:The importance of combinatorial control[J].Plant Physiology,1998,118(4):1 111-1 120.
[13]Thum K E,Kim M,Morishige D T,et al.Analysis of barley chloroplast psb D light-responsive promoter elements intransplastomic tobacco[J].Plant Molecular Biology,2001,47(3):353-366.
[14]Xu N,Hagen G,Guilfoyle T.Multiple auxin response modules in the soybean SAUR15A promoter[J].Plant Science,1997,126(2):193-201.
[15]Xue G P.The DNA-binding activity of an AP2 transcriptional activator Hv CBF2 involved in regulation of low-temperatureresponsive genes in barley is modulated by temperature[J].Plant Journal,2003,33(2):373-383.
[16]Yanagisawa S,Schmidt R J.Diversity and similarity among recognition sequences of Dof transcription factors[J].PlantJournal,1999,17(2):209-214.