期刊文献+

RNA聚合酶Ⅱ动态调控及其成像技术的研究进展 被引量:4

Recent Advances on Dynamic Regulation and Imaging Techniques of RNA Polymerase Ⅱ
下载PDF
导出
摘要 RNA聚合酶Ⅱ(RNA polymerase Ⅱ,RNAP Ⅱ或Pol Ⅱ)在调节生物生长发育和响应环境变化中发挥着重要的作用。转录工厂是细胞核RNA聚合酶Ⅱ集合的位点,多个基因被招募到转录工厂发生共转录,形成一个高度动态协调的过程。尽管真核生物转录过程中RNA聚合酶Ⅱ的重要功能已经被广泛研究,但是植物RNAP Ⅱ在不同生理条件下的活体动态特征仍然知之甚少。活细胞单分子成像技术和分子标记技术的发展,将有助于提升人们对植物RNAP Ⅱ的活体动态特征的新认识。主要阐述了真核生物RNAP Ⅱ的结构和功能特点,并介绍了细胞核内RNAP Ⅱ的动态调控转录机制,重点总结了活细胞内RNAP Ⅱ的动态标记和成像技术的研究进展,以期为今后开展植物RNAP Ⅱ的动态调控研究提供理论依据。 RNA polymerase Ⅱ(RNAP Ⅱ or Pol Ⅱ)plays a vital role in regulating the growth and development of organisms and responding to environmental changes.RNA polymerase Ⅱ assembles and locates at transcription factory,where multiple genes are recruited for the formation of co-transcription,which is a highly dynamic and coordinated process.Although the critical functions of RNA polymerase Ⅱ in eukaryotic gene transcription have been widely studied,the dynamic characteristics of plant RNAP Ⅱ under different physiological conditions are still poorly understood.The development of single-molecule imaging and labeling techniques in living cell will contribute to improving our new understanding of the dynamic characteristics of plant RNAP Ⅱ in vivo.In this review,we mainly expound the structural and functional characteristics of RNAP Ⅱ,and introduce the dynamic regulation and transcription mechanism of RNAP Ⅱ.Furthermore,we put the emphasis on summarizing the recent progresses in dynamic labeling and imaging techniques of RNAP Ⅱ in living cells,aiming to provide theoretical basis for further studies on the dynamic regulation of RNAP Ⅱ in plant.
作者 钱虹萍 陈博 林金星 崔亚宁 QIAN Hong-ping;CHEN Bo;LIN Jin-xing;CUI Ya-ning(Beijing Advanced Innovation Center for Tree Breeding by Molecular Design,Beijing Forestry University,Beijing 100083;College of Biological Sciences&Biotechnology,Beijing Forestry University,Beijing 100083)
出处 《生物技术通报》 CAS CSCD 北大核心 2021年第4期293-302,共10页 Biotechnology Bulletin
基金 国家自然科学基金项目(31530084) 北京林业大学科技创新计划项目(BLX201911)。
关键词 转录工厂 动态标记技术 单分子活体成像技术 调控机制 transcription factory dynamic labeling technology imaging technique of single-molecule in vivo regulatory mechanism
  • 相关文献

参考文献17

二级参考文献177

  • 1ZHANG Yunhai1, PAN Dengke1,2, SUN Xiuzhu1, SUN Guojie1, WANG Xiaobo1, LIU Xiaohui1, LI Yan1, DAI Yunping1 & LI Ning1 1. State Key Laboratory for Agrobiotechnology, China Agricultural University, Beijing 100094, China,2. College of Animal Science and Technology, China Agricultural University, Beijing 100094, China.Production of porcine cloned transgenic embryos expressing green fluorescent protein by somatic cell nuclear transfer[J].Science China(Life Sciences),2006,49(2):164-171. 被引量:10
  • 2郭晓强,王江雁,王仁杰.真核mRNA转录终止机制[J].细胞生物学杂志,2005,27(4):400-402. 被引量:1
  • 3D'Alessio JA et al. Core promoter recognition complex changes accompany liver development. Proc Natl Acad Sci USA, 2011, 108:3906-3911. 被引量:1
  • 4Deato MD et al. MyoD targets TAF3/TRF3 to activate myogenin transcription. Mol Cell, 2008, 32:96-105. 被引量:1
  • 5Yao J et al. Subnuclear segregation of genes and core promoter factors in myogenesis. Genes Dev, 2011, 25:569-580. 被引量:1
  • 6Roeder RG. The role of general initiation factors in transcription by RNA polymerase II. Trends Biochem Sci, 1996, 21 : 327-335. 被引量:1
  • 7Manzano-Winkler B et al. TFII! is required for transcription of the naturally TATA-Iess but initiator-containing V[3 promoter. J Biol Chem, 1996, 271:12076-12081. 被引量:1
  • 8Martinez E et al. Core promoter-specific function of a mutant transcription factor TFIID defective in TATA-box binding. Proc NatlAcadSci USA, 1995, 92:11864-11868. 被引量:1
  • 9Ince TA et al. A conserved downstream element defines a new class of RNA polymerase II promoters. J Biol Chem, 1995, 270: 30249-30252. 被引量:1
  • 10George AA et al. Transcription regulation from a TATA and INR- less promoter: spatial segregation of promoter function. EMBO J, 2006, 25:811-821. 被引量:1

共引文献424

同被引文献44

引证文献4

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部