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枯草芽孢杆菌新型RNA聚合酶对启动子选择的改变

Altered promoter selection by a novel form of Bacillus subtilis RNA polymerase.

作者信息

Jaehning J A, Wiggs J L, Chamberlin M J

出版信息

Proc Natl Acad Sci U S A. 1979 Nov;76(11):5470-4. doi: 10.1073/pnas.76.11.5470.

Abstract

Bacillus subtilis RNA polymerase holoenzyme prepared by several standard methods utilizes bacteriophage T7 DeltaD111 DNA as an efficient template. The major RNA products are specific transcripts from T7 promoters A(1) and C; these promoters are also efficiently utilized by RNA polymerases purified from a wide range of other bacterial species [Wiggs, J., Bush, J. & Chamberlin, M. (1979) Cell 16, 97-109]. In contrast, B. subtilis RNA polymerase preparations purified by a modification of the method of Burgess and Jendrisak (designated fraction 5) utilize T7 DeltaD111 promoters A(1) and C and an additional promoter site, J, which has been located at 90.6% on the standard T7 physical map. This promoter is not used by B. subtilis core RNA polymerase or by RNA polymerase from any other bacterial species we have tested. Sodium dodecyl sulfate/polyacrylamide gel electrophoresis of fraction 5 RNA polymerase shows that it contains B. subtilis components sigma and delta and a polypeptide of M(r) 92,000 in addition to the B. subtilis beta, beta', and alpha subunits. Chromatography of fraction 5 on single-stranded DNA-cellulose gives an enzyme fraction, Bs I, that is indistinguishable from B. subtilis RNA polymerase holoenzyme both in its peptide composition (betabeta'alpha(2)sigma) and in the selective transcription of only T7 RNAs A(1) and C. Chromatography of fraction 5 on phosphocellulose yields an enzyme fraction, Bs II, devoid of sigma subunit but containing the M(r) 92,000 peptide and traces of delta. This fraction synthesizes predominantly T7 J RNA in vitro together with traces of T7 A(1) and C RNAs. Hence, B. subtilis RNA polymerase fraction Bs II appears to contain a form of RNA polymerase that can transcribe selectively without detectable amounts of B. subtilis sigma subunit and that utilizes a promoter site not used by other known bacterial RNA polymerases. The structural basis for this specificity is not yet known.

摘要

通过几种标准方法制备的枯草芽孢杆菌RNA聚合酶全酶可将噬菌体T7 ΔD111 DNA用作高效模板。主要的RNA产物是来自T7启动子A(1)和C的特异性转录本;这些启动子也被从多种其他细菌物种中纯化的RNA聚合酶有效利用[威格斯,J.,布什,J.和钱伯林,M.(1979年)《细胞》16卷,97 - 109页]。相比之下,通过对伯吉斯和延德里萨克方法进行改进而纯化的枯草芽孢杆菌RNA聚合酶制剂(称为组分5)利用T7 ΔD111启动子A(1)和C以及一个额外的启动子位点J,该位点位于标准T7物理图谱的90.6%处。这个启动子不被枯草芽孢杆菌核心RNA聚合酶或我们测试过的任何其他细菌物种的RNA聚合酶所使用。组分5 RNA聚合酶的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳显示,除了枯草芽孢杆菌的β、β'和α亚基外,它还含有枯草芽孢杆菌组分σ和δ以及一个分子量为92,000的多肽。组分5在单链DNA - 纤维素上进行色谱分离得到一种酶组分Bs I,其肽组成(ββ'α(2)σ)以及仅对T7 RNA A(1)和C的选择性转录与枯草芽孢杆菌RNA聚合酶全酶没有区别。组分5在磷酸纤维素上进行色谱分离得到一种酶组分Bs II,它不含σ亚基,但含有分子量为92,000的肽和微量的δ。该组分在体外主要合成T7 J RNA以及微量的T7 A(1)和C RNA。因此,枯草芽孢杆菌RNA聚合酶组分Bs II似乎含有一种RNA聚合酶形式,它可以在没有可检测量的枯草芽孢杆菌σ亚基的情况下进行选择性转录,并且利用一个其他已知细菌RNA聚合酶未使用的启动子位点。这种特异性的结构基础尚不清楚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c23f/411670/a434e6714745/pnas00011-0065-a.jpg

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