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1
PCR mutagenesis identifies a polymerase-binding sequence of sigma 54 that includes a sigma 70 homology region.聚合酶链式反应诱变鉴定出σ54的一个聚合酶结合序列,该序列包含一个σ70同源区域。
J Bacteriol. 1995 Oct;177(20):5818-25. doi: 10.1128/jb.177.20.5818-5825.1995.
2
DNA-binding determinants of sigma 54 as deduced from libraries of mutations.从突变文库推导的σ54的DNA结合决定因素。
J Bacteriol. 1997 Feb;179(4):1239-45. doi: 10.1128/jb.179.4.1239-1245.1997.
3
RNA polymerase binding using a strongly acidic hydrophobic-repeat region of sigma 54.利用σ54的强酸性疏水重复区域进行RNA聚合酶结合。
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2120-4. doi: 10.1073/pnas.91.6.2120.
4
The hydrophobic heptad repeat in Region III of Escherichia coli transcription factor sigma 54 is essential for core RNA polymerase binding.大肠杆菌转录因子σ54第三区域中的疏水七肽重复序列对于核心RNA聚合酶的结合至关重要。
Microbiology (Reading). 1999 Nov;145 ( Pt 11):3081-3088. doi: 10.1099/00221287-145-11-3081.
5
Mutagenesis of region 4 of sigma 28 from Chlamydia trachomatis defines determinants for protein-protein and protein-DNA interactions.沙眼衣原体σ28第4区域的诱变确定了蛋白质-蛋白质和蛋白质-DNA相互作用的决定因素。
J Bacteriol. 2009 Jan;191(2):651-60. doi: 10.1128/JB.01083-08. Epub 2008 Oct 31.
6
Mutations in the 1.1 subdomain of Escherichia coli sigma factor sigma70 and disruption of its overall structure.大肠杆菌σ因子σ70的1.1亚结构域中的突变及其整体结构的破坏。
Eur J Biochem. 1997 Mar 1;244(2):613-8. doi: 10.1111/j.1432-1033.1997.00613.x.
7
Mutational analysis of beta '260-309, a sigma 70 binding site located on Escherichia coli core RNA polymerase.β'260 - 309的突变分析,β'260 - 309是位于大肠杆菌核心RNA聚合酶上的一个σ70结合位点。
J Biol Chem. 2000 Jul 28;275(30):23113-9. doi: 10.1074/jbc.M002040200.
8
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。
Biochemistry. 1998 Mar 10;37(10):3312-20. doi: 10.1021/bi972041m.
9
Characterization of the Escherichia coli transcription factor sigma 70: localization of a region involved in the interaction with core RNA polymerase.大肠杆菌转录因子σ70的特性:与核心RNA聚合酶相互作用相关区域的定位
Biochemistry. 1989 Sep 19;28(19):7728-34. doi: 10.1021/bi00445a031.
10
Mapping the molecular interface between the sigma(70) subunit of E. coli RNA polymerase and T4 AsiA.绘制大肠杆菌RNA聚合酶σ(70)亚基与T4 AsiA之间的分子界面
J Mol Biol. 2001 Mar 2;306(4):631-42. doi: 10.1006/jmbi.2001.4445.

引用本文的文献

1
Structure of the RNA polymerase core-binding domain of sigma(54) reveals a likely conformational fracture point.σ54的RNA聚合酶核心结合结构域的结构揭示了一个可能的构象断裂点。
J Mol Biol. 2009 Jul 3;390(1):70-82. doi: 10.1016/j.jmb.2009.04.070. Epub 2009 May 5.
2
When coupled to natural transformation in Acinetobacter sp. strain ADP1, PCR mutagenesis is made less random by mismatch repair.当与不动杆菌属ADP1菌株中的自然转化相结合时,错配修复会降低PCR诱变的随机性。
Appl Environ Microbiol. 2005 Nov;71(11):7610-2. doi: 10.1128/AEM.71.11.7610-7612.2005.
3
Single amino acid substitution mutants of Klebsiella pneumoniae sigma(54) defective in transcription.肺炎克雷伯菌σ因子(54)中在转录方面存在缺陷的单氨基酸取代突变体。
Nucleic Acids Res. 2000 Nov 15;28(22):4419-27. doi: 10.1093/nar/28.22.4419.
4
Transcription initiation-defective forms of sigma(54) that differ in ability To function with a heteroduplex DNA template.在与异源双链DNA模板发挥功能的能力上存在差异的σ(54)转录起始缺陷形式。
J Bacteriol. 2000 Nov;182(22):6503-8. doi: 10.1128/JB.182.22.6503-6508.2000.
5
Identifying a core RNA polymerase surface critical for interactions with a sigma-like specificity factor.鉴定对与类σ特异性因子相互作用至关重要的核心RNA聚合酶表面。
Mol Cell Biol. 2000 Sep;20(18):7013-23. doi: 10.1128/MCB.20.18.7013-7023.2000.
6
The bacterial enhancer-dependent sigma(54) (sigma(N)) transcription factor.细菌增强子依赖性σ(54)(σ(N))转录因子。
J Bacteriol. 2000 Aug;182(15):4129-36. doi: 10.1128/JB.182.15.4129-4136.2000.
7
The role of region II in the RNA polymerase sigma factor sigma(N) (sigma(54)).区域II在RNA聚合酶σ因子σ(N)(σ54)中的作用。
Nucleic Acids Res. 2000 Jul 1;28(13):2563-70. doi: 10.1093/nar/28.13.2563.
8
Conservation of sigma-core RNA polymerase proximity relationships between the enhancer-independent and enhancer-dependent sigma classes.增强子非依赖型和增强子依赖型σ因子类别之间σ核心RNA聚合酶邻近关系的保守性。
EMBO J. 2000 Jun 15;19(12):3038-48. doi: 10.1093/emboj/19.12.3038.
9
Reciprocal domain evolution within a transactivator in a restricted sequence space.在受限序列空间中反式激活因子内的互反结构域进化。
Proc Natl Acad Sci U S A. 2000 Mar 28;97(7):3314-8. doi: 10.1073/pnas.97.7.3314.
10
The amino terminus of Salmonella enterica serovar Typhimurium sigma(54) is required for interactions with an enhancer-binding protein and binding to fork junction DNA.鼠伤寒沙门氏菌σ(54)的氨基末端是与增强子结合蛋白相互作用及与叉状连接DNA结合所必需的。
J Bacteriol. 2000 Jan;182(2):513-7. doi: 10.1128/JB.182.2.513-517.2000.

本文引用的文献

1
Functional roles for the glutamines within the glutamine-rich region of the transcription factor sigma 54.转录因子σ54富含谷氨酰胺区域内谷氨酰胺的功能作用。
J Biol Chem. 1994 Jan 7;269(1):373-8.
2
RNA polymerase binding using a strongly acidic hydrophobic-repeat region of sigma 54.利用σ54的强酸性疏水重复区域进行RNA聚合酶结合。
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2120-4. doi: 10.1073/pnas.91.6.2120.
3
The domain structure of sigma 54 as determined by analysis of a set of deletion mutants.通过对一组缺失突变体的分析确定的σ54的结构域结构。
J Mol Biol. 1994 Feb 11;236(1):81-90. doi: 10.1006/jmbi.1994.1120.
4
Novel proteins of the phosphotransferase system encoded within the rpoN operon of Escherichia coli. Enzyme IIANtr affects growth on organic nitrogen and the conditional lethality of an erats mutant.大肠杆菌rpoN操纵子内编码的磷酸转移酶系统的新型蛋白质。酶IIANtr影响有机氮上的生长以及erats突变体的条件致死性。
J Biol Chem. 1995 Mar 3;270(9):4822-39. doi: 10.1074/jbc.270.9.4822.
5
Physical and genetic characterization of the glnA--glnG region of the Escherichia coli chromosome.大肠杆菌染色体谷氨酰胺合成酶基因(glnA)-谷氨酰胺合成酶基因激活蛋白基因(glnG)区域的物理和遗传特征分析
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3743-7. doi: 10.1073/pnas.78.6.3743.
6
The nucleotide sequence of the nitrogen-regulation gene ntrA of Klebsiella pneumoniae and comparison with conserved features in bacterial RNA polymerase sigma factors.肺炎克雷伯菌氮调节基因ntrA的核苷酸序列及其与细菌RNA聚合酶σ因子保守特征的比较。
Nucleic Acids Res. 1985 Nov 11;13(21):7607-20. doi: 10.1093/nar/13.21.7607.
7
Transcription of glnA in E. coli is stimulated by activator bound to sites far from the promoter.在大肠杆菌中,谷氨酰胺合成酶基因(glnA)的转录受到与远离启动子的位点结合的激活剂的刺激。
Cell. 1986 Jun 20;45(6):785-92. doi: 10.1016/0092-8674(86)90553-2.
8
Transcription of glnA by purified Escherichia coli components: core RNA polymerase and the products of glnF, glnG, and glnL.用纯化的大肠杆菌成分转录谷氨酰胺合成酶基因A:核心RNA聚合酶以及谷氨酰胺合成酶基因F、谷氨酰胺合成酶基因G和谷氨酰胺合成酶基因L的产物。
Proc Natl Acad Sci U S A. 1985 Dec;82(24):8453-7. doi: 10.1073/pnas.82.24.8453.
9
Characterization of the Escherichia coli transcription factor sigma 70: localization of a region involved in the interaction with core RNA polymerase.大肠杆菌转录因子σ70的特性:与核心RNA聚合酶相互作用相关区域的定位
Biochemistry. 1989 Sep 19;28(19):7728-34. doi: 10.1021/bi00445a031.
10
Expression of sigma 54 (ntrA)-dependent genes is probably united by a common mechanism.σ54(ntrA)依赖性基因的表达可能由一种共同机制统一起来。
Microbiol Rev. 1989 Sep;53(3):367-76. doi: 10.1128/mr.53.3.367-376.1989.

聚合酶链式反应诱变鉴定出σ54的一个聚合酶结合序列,该序列包含一个σ70同源区域。

PCR mutagenesis identifies a polymerase-binding sequence of sigma 54 that includes a sigma 70 homology region.

作者信息

Tintut Y, Gralla J D

机构信息

Department of Chemistry and Biochemistry, University of California, Los Angeles 90095, USA.

出版信息

J Bacteriol. 1995 Oct;177(20):5818-25. doi: 10.1128/jb.177.20.5818-5825.1995.

DOI:10.1128/jb.177.20.5818-5825.1995
PMID:7592329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC177404/
Abstract

Sigma 54 is a minor bacterial sigma factor that is not a member of the sigma 70 family of proteins but binds the same core RNA polymerase. Previously, we identified a region of sigma 54 that is important for binding core polymerase. In this work, PCR mutagenesis was used to identify specific amino acids important for this binding. The results show that important residues are clustered most closely in a short sequence that was previously speculated to be potentially homologous to a sequence in sigma 70. The mutagenesis also identifies important residues in the flanking hydrophobic-acidic region of sigma 54, which is absent in sigma 70. Overall, the data indicate that sigma 54 binds core polymerase through a sequence homologous to that of sigma 70 but in addition uses unique motifs to modify this interaction.

摘要

σ54是一种次要的细菌σ因子,它不是σ70蛋白家族的成员,但能结合相同的核心RNA聚合酶。此前,我们鉴定出σ54中对结合核心聚合酶很重要的一个区域。在这项研究中,利用PCR诱变来鉴定对这种结合很重要的特定氨基酸。结果表明,重要残基最紧密地聚集在一个短序列中,该序列此前被推测可能与σ70中的一个序列同源。诱变还鉴定出了σ54侧翼疏水-酸性区域中的重要残基,这一区域在σ70中不存在。总体而言,数据表明σ54通过与σ70同源的序列结合核心聚合酶,但此外还利用独特的基序来修饰这种相互作用。