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1
The role of TFIIB-RNA polymerase II interaction in start site selection in yeast cells.TFIIB与RNA聚合酶II的相互作用在酵母细胞起始位点选择中的作用。
Nucleic Acids Res. 2002 Jul 15;30(14):3078-85. doi: 10.1093/nar/gkf422.
2
The N-terminal region of yeast TFIIB contains two adjacent functional domains involved in stable RNA polymerase II binding and transcription start site selection.酵母TFIIB的N端区域包含两个相邻的功能域,它们参与稳定的RNA聚合酶II结合以及转录起始位点的选择。
J Biol Chem. 1998 Jul 10;273(28):17859-64. doi: 10.1074/jbc.273.28.17859.
3
Mechanism of start site selection by RNA polymerase II: interplay between TFIIB and Ssl2/XPB helicase subunit of TFIIH.RNA 聚合酶 II 启动子选择的机制:TFIIB 和 TFIIH 的 Ssl2/XPB 解旋酶亚基之间的相互作用。
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4
Mutational analysis of the D1/E1 core helices and the conserved N-terminal region of yeast transcription factor IIB (TFIIB): identification of an N-terminal mutant that stabilizes TATA-binding protein-TFIIB-DNA complexes.酵母转录因子IIB(TFIIB)的D1/E1核心螺旋和保守N端区域的突变分析:鉴定一种能稳定TATA结合蛋白-TFIIB-DNA复合物的N端突变体。
Mol Cell Biol. 1997 Dec;17(12):6784-93. doi: 10.1128/MCB.17.12.6784.
5
Promoter-specific shifts in transcription initiation conferred by yeast TFIIB mutations are determined by the sequence in the immediate vicinity of the start sites.酵母TFIIB突变导致的转录起始位点特异性转移由起始位点紧邻区域的序列决定。
Mol Cell Biol. 2001 Jul;21(14):4427-40. doi: 10.1128/MCB.21.14.4427-4440.2001.
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Functional interaction between TFIIB and the Rpb9 (Ssu73) subunit of RNA polymerase II in Saccharomyces cerevisiae.酿酒酵母中TFIIB与RNA聚合酶II的Rpb9(Ssu73)亚基之间的功能相互作用。
Nucleic Acids Res. 1996 Jul 1;24(13):2560-6. doi: 10.1093/nar/24.13.2560.
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The sua8 suppressors of Saccharomyces cerevisiae encode replacements of conserved residues within the largest subunit of RNA polymerase II and affect transcription start site selection similarly to sua7 (TFIIB) mutations.酿酒酵母的sua8抑制子编码RNA聚合酶II最大亚基内保守残基的替换,并且与sua7(TFIIB)突变类似地影响转录起始位点的选择。
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High-resolution protein-DNA contacts for the yeast RNA polymerase II general transcription machinery.酵母RNA聚合酶II通用转录机制的高分辨率蛋白质-DNA相互作用。
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Intramolecular interaction of yeast TFIIB in transcription control.酵母TFIIB在转录调控中的分子内相互作用。
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Recruitment of TBP or TFIIB to a promoter proximal position leads to stimulation of RNA polymerase II transcription without activator proteins both in vivo and in vitro.在体内和体外,TBP 或 TFIIB 募集到启动子近端位置都会在没有激活蛋白的情况下刺激 RNA 聚合酶 II 的转录。
Biochem Biophys Res Commun. 1999 Mar 5;256(1):45-51. doi: 10.1006/bbrc.1999.0280.

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TFIIH generates a six-base-pair open complex during RNAP II transcription initiation and start-site scanning.TFIIH在RNA聚合酶II转录起始和起始位点扫描过程中产生一个六碱基对的开放复合物。
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Relationships of RNA polymerase II genetic interactors to transcription start site usage defects and growth in Saccharomyces cerevisiae.RNA 聚合酶 II 遗传互作因子与酿酒酵母转录起始位点使用缺陷和生长的关系。
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Dissection of Pol II trigger loop function and Pol II activity-dependent control of start site selection in vivo.体内 Pol II 触发环功能的剖析和 Pol II 活性依赖性启动子选择的控制。
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6
Evidence that RNA polymerase II and not TFIIB is responsible for the difference in transcription initiation patterns between Saccharomyces cerevisiae and Schizosaccharomyces pombe.证据表明,RNA 聚合酶 II 而不是 TFIIB 负责酿酒酵母和裂殖酵母转录起始模式的差异。
Nucleic Acids Res. 2012 Aug;40(14):6495-507. doi: 10.1093/nar/gks323. Epub 2012 Apr 17.
7
Mechanism of start site selection by RNA polymerase II: interplay between TFIIB and Ssl2/XPB helicase subunit of TFIIH.RNA 聚合酶 II 启动子选择的机制:TFIIB 和 TFIIH 的 Ssl2/XPB 解旋酶亚基之间的相互作用。
J Biol Chem. 2012 Jan 2;287(1):557-567. doi: 10.1074/jbc.M111.281576. Epub 2011 Nov 11.
8
RNA polymerase II-TFIIB structure and mechanism of transcription initiation.RNA聚合酶II - TFIIB转录起始的结构与机制
Nature. 2009 Nov 19;462(7271):323-30. doi: 10.1038/nature08548.
9
Control of the timing of promoter escape and RNA catalysis by the transcription factor IIb fingertip.转录因子IIb指尖对启动子逃逸和RNA催化时机的调控。
J Biol Chem. 2008 Jun 6;283(23):15665-71. doi: 10.1074/jbc.M801439200. Epub 2008 Apr 14.
10
Functions of Saccharomyces cerevisiae TFIIF during transcription start site utilization.酿酒酵母TFIIF在转录起始位点利用过程中的功能。
Mol Cell Biol. 2008 Jun;28(11):3757-66. doi: 10.1128/MCB.02272-07. Epub 2008 Mar 24.

本文引用的文献

1
Promoter-specific shifts in transcription initiation conferred by yeast TFIIB mutations are determined by the sequence in the immediate vicinity of the start sites.酵母TFIIB突变导致的转录起始位点特异性转移由起始位点紧邻区域的序列决定。
Mol Cell Biol. 2001 Jul;21(14):4427-40. doi: 10.1128/MCB.21.14.4427-4440.2001.
2
Structural basis of transcription: an RNA polymerase II elongation complex at 3.3 A resolution.转录的结构基础:分辨率为3.3埃的RNA聚合酶II延伸复合物
Science. 2001 Jun 8;292(5523):1876-82. doi: 10.1126/science.1059495. Epub 2001 Apr 19.
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Structural basis of transcription: RNA polymerase II at 2.8 angstrom resolution.转录的结构基础:分辨率为2.8埃的RNA聚合酶II
Science. 2001 Jun 8;292(5523):1863-76. doi: 10.1126/science.1059493. Epub 2001 Apr 19.
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RNA polymerase II subunit Rpb9 regulates transcription elongation in vivo.
J Biol Chem. 2000 Nov 10;275(45):35506-11. doi: 10.1074/jbc.M004721200.
5
Artificially recruited TATA-binding protein fails to remodel chromatin and does not activate three promoters that require chromatin remodeling.人工招募的TATA结合蛋白无法重塑染色质,也不能激活三个需要染色质重塑的启动子。
Mol Cell Biol. 2000 Aug;20(16):5847-57. doi: 10.1128/MCB.20.16.5847-5857.2000.
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Intramolecular interaction of yeast TFIIB in transcription control.酵母TFIIB在转录调控中的分子内相互作用。
Nucleic Acids Res. 2000 May 1;28(9):1913-20. doi: 10.1093/nar/28.9.1913.
7
Rad25p, a DNA helicase subunit of yeast transcription factor TFIIH, is required for promoter escape in vivo.Rad25p是酵母转录因子TFIIH的一种DNA解旋酶亚基,在体内启动子逃逸过程中是必需的。
Gene. 2000 Mar 7;245(1):109-17. doi: 10.1016/s0378-1119(00)00029-9.
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The conformation of the transcription factor TFIIB modulates the response to transcriptional activators in vivo.转录因子TFIIB的构象在体内调节对转录激活因子的反应。
Curr Biol. 2000 Mar 9;10(5):273-6. doi: 10.1016/s0960-9822(00)00363-8.
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Yeast RNA polymerase II subunit RPB9. Mapping of domains required for transcription elongation.酵母RNA聚合酶II亚基RPB9。转录延伸所需结构域的定位。
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10
Mutational analysis of yeast TFIIB. A functional relationship between Ssu72 and Sub1/Tsp1 defined by allele-specific interactions with TFIIB.酵母TFIIB的突变分析。通过与TFIIB的等位基因特异性相互作用定义的Ssu72与Sub1/Tsp1之间的功能关系。
Genetics. 1999 Oct;153(2):643-52. doi: 10.1093/genetics/153.2.643.

TFIIB与RNA聚合酶II的相互作用在酵母细胞起始位点选择中的作用。

The role of TFIIB-RNA polymerase II interaction in start site selection in yeast cells.

作者信息

Zhang Dong-Yi, Carson Daniel J, Ma Jun

机构信息

Division of Developmental Biology, Children's Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

出版信息

Nucleic Acids Res. 2002 Jul 15;30(14):3078-85. doi: 10.1093/nar/gkf422.

DOI:10.1093/nar/gkf422
PMID:12136090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC135743/
Abstract

Previous studies have established a critical role of both TFIIB and RNA polymerase II (RNAPII) in start site selection in the yeast Saccharomyces cerevisiae. However, it remains unclear how the TFIIB-RNAPII interaction impacts on this process since such an interaction can potentially influence both preinitiation complex (PIC) stability and conformation. In this study, we further investigate the role of TFIIB in start site selection by characterizing our newly generated TFIIB mutants, two of which exhibit a novel upstream shift of start sites in vivo. We took advantage of an artificial recruitment system in which an RNAPII holoenzyme component is covalently linked to a DNA-binding domain for more direct and stable recruitment. We show that TFIIB mutations can exert their effects on start site selection in such an artificial recruitment system even though it has a relaxed requirement for TFIIB. We further show that these TFIIB mutants have normal affinity for RNAPII and do not alter the promoter melting/scanning step. Finally, we show that overexpressing the genetically isolated TFIIB mutant E62K, which has a reduced affinity for RNAPII, can correct its start site selection defect. We discuss a model in which the TFIIB-RNAPII interaction controls the start site selection process by influencing the conformation of PIC prior to or during PIC assembly, as opposed to PIC stability.

摘要

先前的研究已经证实,转录因子IIB(TFIIB)和RNA聚合酶II(RNAPII)在酿酒酵母起始位点选择过程中都起着关键作用。然而,TFIIB与RNAPII之间的相互作用如何影响这一过程仍不清楚,因为这种相互作用可能会潜在地影响起始前复合物(PIC)的稳定性和构象。在本研究中,我们通过对新构建的TFIIB突变体进行表征,进一步探究了TFIIB在起始位点选择中的作用,其中两个突变体在体内表现出起始位点的新型上游移位。我们利用了一种人工招募系统,在该系统中,RNAPII全酶组分与一个DNA结合结构域共价连接,以实现更直接和稳定的招募。我们发现,尽管该人工招募系统对TFIIB的要求较为宽松,但TFIIB突变体仍能在此系统中对起始位点选择产生影响。我们进一步表明,这些TFIIB突变体对RNAPII具有正常的亲和力,并且不会改变启动子解链/扫描步骤。最后,我们发现过表达对RNAPII亲和力降低但经基因分离的TFIIB突变体E62K,可以纠正其起始位点选择缺陷。我们讨论了一个模型,其中TFIIB-RNAPII相互作用通过在PIC组装之前或期间影响PIC的构象来控制起始位点选择过程,而不是通过影响PIC的稳定性。