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基因AtHsp17.6-C2启动子的克隆及其热诱导动力学研究(英文)

Clonning the Promoter of AtHsp17.6-C2 and Its Heat Inducible Kinetics

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【作者】 曾卫军王水平李小方徐萍王瑞刚

【Author】 ZENG Wei-jun1,2WANG Shui-ping1LI Xiao-fang1XU Ping3WANG Rui-gang4(1 School of Life Science,East China Normal University,Shanghai200062,China)(2 College of Life Science and Chemistry,Xinjiang Normal University,Urumqi830054,China)(3 Shanghai Information Center for Life Science,CAS,Shanghai200031,China)(4 College of Life Sciences,Inner Mongolia Agricultural University,Huhhot010018,China)

【机构】 华东师范大学生命科学学院新疆师范大学生命科学与化学学院中国科学院上海生命科学信息中心内蒙古农业大学生命科学学院

【摘要】 介绍一个植物表达系统,由热激蛋白基因(AtHsp17.6-C2)的启动子来驱动GUS基因的表达。在22℃生长条件下,稳定遗传的转基因植株中几乎检测不到GUS的活性。但是当温度升至34~37℃时,GUS的活性迅速升高。37℃是该植物表达系统最适诱导温度。转基因植株经37℃热诱导2小时后再返回22℃培育2小时,GUS的活性增加80多倍。多次热诱导实验表明这个表达系统是能够被重复多次热诱导的。实验结果表明这个植物诱导表达系统能够适用于多种目的需要。

【Abstract】 A gene expression system were constructed,driven by a heat-shock gene promoter(AtHsp17.6-C2),to control the expression of reporter gene(GUS)in transgenic plants.The expression of the AtHsp17.6-C2 chimeric gene in the stable transformants of ⊿F1-22-13 was hardly detected in culture at 22℃.However,the expression increased dramatically at the transcriptional level when the incubation temperature was shifted to 34~37℃.The optimal temperature for heat(shock)induction was 37℃.After a 2h incubation at 37℃ and 2h recovery phase at 22℃,GUS activity was about 80 fold greater than that before heat shock.Multiple heat-shock treatments showed that this system was heat reinducible.This new system can be applied in numerous and various applications.

【基金】 supported by The Project-sponsored by SRF for ROCS,SEM.(2006);grants from Natural Scientific Foundation of China(30660014);Natural Scientific Foundation of Inner Mongolia(200508010503)~~
  • 【文献出处】 中国生物工程杂志 ,China Biotechnology , 编辑部邮箱 ,2010年06期
  • 【分类号】Q786
  • 【被引频次】1
  • 【下载频次】114
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