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原核生物转录调控研究技术及进展 被引量:1

Research Technology and Progress in Transcriptional Regulation in Prokaryotes
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摘要 原核生物基因表达调控主要发生在转录水平,研究原核生物的转录调控有利于了解其基因表达调节机制。近年来,随着分子生物学及相关技术的突破,转录调控研究技术也不断发展,因此主要综述了原核生物转录调控的技术方法及其新进展,包括凝胶电泳迁移率实验、DNase I足迹技术、染色质免疫共沉淀技术、微量热泳动技术、等温滴定量热法及细菌单杂交系统,以期系统地了解这些方法的优缺点和适用性,帮助研究者更好的利用原核生物转录调控为人类造福。 The regulation of gene expression in prokaryotes mainly occurs at the transcriptional level.Knowledge on the regulation of transcription in prokaryotes is conducive to understanding the mechanism of gene expression regulation.In recent years,with the breakthrough of molecular biology and related technologies,the research technology of transcriptional regulation has also been continuously developed.The technical methods and new developments of prokaryotic transcriptional regulation are reviewed in the present study,including electrophoretic mobility shift assay,DNase I footprinting technology,chromatin immunoprecipitation technology,microthermophoresis technology,isothermal titration calorimetry and bacterial one hybrid system,aiming to systematically understand the advantages/disadvantages and suitability of these methods,help researchers to better use the transcriptional regulation of prokaryotes for bringing great benefits to human life.
作者 陈臣 黄芝阳 于海燕 袁海彬 田怀香 CHEN Chen;HUANG Zhi-yang;YU Hai-yan;YUAN Hai-bin;TIAN Huai-xiang(School of Perfume and Aroma Technology,Shanghai Institute of Technology,Shanghai 201418)
出处 《生物技术通报》 CAS CSCD 北大核心 2022年第10期54-65,共12页 Biotechnology Bulletin
基金 国家自然科学基金面上项目(31972197)。
关键词 转录调控 相互作用 启动子 转录因子 转录因子结合位点 transcriptional regulation interaction promoter transcription factor transcription factor binding site
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  • 1蒲泽锦,吴灵飞.核因子-κB电泳迁移率变动分析方法的改进[J].汕头大学医学院学报,2005,18(3):169-171. 被引量:3
  • 2孙宇,贾凌云,任军.蛋白质相互作用的研究方法[J].分析化学,2007,35(5):760-766. 被引量:11
  • 3Galas D,Schmitz A.DNase footprinting: a simple method for the detection of protein-DNA binding specificity[].Nucleic Acids Research.1978
  • 4Ausubel F.Current Protocols in Molecular Biology[]..1997
  • 5Sandaltzopoulos R,Becker P B.Solid phase DNaseⅠfootprinting:quick and versatile[].Nucleic Acids Research.1994
  • 6Dignam J D,Lebovitz R M,Roeder R G.Accurate transcription initiation by RNA polymerase Ⅱ in a soluble extract from isolated mammalian nuclei[].Nucleic Acids Research.1983
  • 7Bannister A, Kouzarides T. Basic peptides enhance protein- DNA interaction in vitro[J]. Nuel Acids Res, 1992,20:3523.
  • 8Sambrook J, Russell D. Molecular cloning: a laboratory manual [J]. 3rd ed. New York: Cold Spring Harbor Laboratory Press, 2001:1322-1336.
  • 9Fried M G, Crothers D M. Kinetics and mechanism in the re- action of gene regulatory proteins with DNA[J]. J Mol Biol, 1984,172:263-282.
  • 10Ellingtion A D, Szostak J W. In vitro selection of RNA mole- cules that bind specific ligands[J]. Nature, 1990,346(6287): 818-822.

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