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大肠杆菌RNA聚合酶对启动子DNA非模板链的碱基特异性识别。

Base-specific recognition of the nontemplate strand of promoter DNA by E. coli RNA polymerase.

作者信息

Roberts C W, Roberts J W

机构信息

Section of Biochemistry, Molecular and Cell Biology Cornell University Ithaca, New York 14853, USA.

出版信息

Cell. 1996 Aug 9;86(3):495-501. doi: 10.1016/s0092-8674(00)80122-1.

DOI:10.1016/s0092-8674(00)80122-1
PMID:8756731
Abstract

RNA polymerase recognizes its promoters through base-specific interaction between defined segments of DNA and the sigma subunit of the enzyme. This interaction leads to separation of base pairs and exposure of the template strand for RNA synthesis. We show that base-specific recognition by the sigma 70 holoenzyme in this process involves primarily nontemplate strand bases in the -10 promoter region. We suggest that melting involves the persistence of these contacts as the bound duplex (closed) form is converted to the single-stranded (open) form of the enzyme-promoter complex.

摘要

RNA聚合酶通过DNA特定片段与该酶的σ亚基之间的碱基特异性相互作用来识别其启动子。这种相互作用导致碱基对分离,并使模板链暴露以进行RNA合成。我们发现,在此过程中,σ70全酶的碱基特异性识别主要涉及-10启动子区域中的非模板链碱基。我们认为,解链涉及这些接触的持续存在,因为结合的双链体(闭合)形式转变为酶-启动子复合物的单链(开放)形式。

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Base-specific recognition of the nontemplate strand of promoter DNA by E. coli RNA polymerase.大肠杆菌RNA聚合酶对启动子DNA非模板链的碱基特异性识别。
Cell. 1996 Aug 9;86(3):495-501. doi: 10.1016/s0092-8674(00)80122-1.
2
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Promoter recognition as measured by binding of polymerase to nontemplate strand oligonucleotide.通过聚合酶与非模板链寡核苷酸的结合来衡量启动子识别。
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Conformation and DNA binding properties of a single-stranded DNA binding region of sigma 70 subunit from Escherichia coli RNA polymerase are modulated by an interaction with the core enzyme.来自大肠杆菌RNA聚合酶σ70亚基单链DNA结合区域的构象和DNA结合特性受与核心酶相互作用的调节。
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