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噬菌体phi 29转录激活因子在病毒晚期启动子中诱导产生的弯曲对于激活是必需的。

Bend induced by the phage phi 29 transcriptional activator in the viral late promoter is required for activation.

作者信息

Rojo F, Zaballos A, Salas M

机构信息

Centro de Biología Molecular (CSIC-UAM) Universidad Autónoma de Madrid, Spain.

出版信息

J Mol Biol. 1990 Feb 20;211(4):713-25. doi: 10.1016/0022-2836(90)90072-t.

DOI:10.1016/0022-2836(90)90072-t
PMID:2107318
Abstract

Transcription initiation from the Bacillus subtilis phage phi 29 late A3 promoter requires the viral protein p4, a transcriptional activator. Protein p4 binds to a region of the A3 promoter, located between nucleotides -50 and -100 relative to the transcription start site, that presents a sequence-directed curvature. This curvature is enhanced when protein p4 binds to the promoter. A number of deletion mutants at the carboxyl end of protein p4 have been constructed and their behavior as transcriptional activators of the late A3 promoter has been investigated. The binding of these deletion mutants to the late A3 promoter has been analyzed by gel retardation, DNase I footprinting, methylation interference and circular permutation assays. The results suggest that the last 12 amino acid residues of protein p4, six of which are positively charged, although not involved in the specific recognition of the promoter are responsible for part of the bend induced by protein p4 in its binding site. Evidence is presented which suggests that full induction of this curvature is needed for the transcription activation process. A model is proposed for protein p4 interaction with the A3 promoter, in which the bend is induced in two steps: first, two monomers of protein p4 bind to the inverted recognition sequences, subsequent interaction between them generating a bend between these sequences; second, the highly basic carboxyl terminus of protein p4 establishes non-specific electrostatic interactions with the DNA backbone inducing a bend at both ends of the protein p4 binding region.

摘要

枯草芽孢杆菌噬菌体φ29晚期A3启动子的转录起始需要病毒蛋白p4,一种转录激活因子。蛋白p4结合到A3启动子的一个区域,该区域位于相对于转录起始位点的核苷酸-50至-100之间,呈现出序列导向的弯曲。当蛋白p4与启动子结合时,这种弯曲会增强。已构建了蛋白p4羧基末端的多个缺失突变体,并研究了它们作为晚期A3启动子转录激活因子的行为。通过凝胶阻滞、DNase I足迹分析、甲基化干扰和环形置换分析,分析了这些缺失突变体与晚期A3启动子的结合情况。结果表明,蛋白p4的最后12个氨基酸残基,其中6个带正电荷,虽然不参与启动子的特异性识别,但负责蛋白p4在其结合位点诱导的部分弯曲。有证据表明,转录激活过程需要这种弯曲的完全诱导。提出了一个蛋白p4与A3启动子相互作用的模型,其中弯曲分两步诱导:首先,蛋白p4的两个单体结合到反向识别序列上,它们之间的后续相互作用在这些序列之间产生一个弯曲;其次,蛋白p4高度碱性的羧基末端与DNA主链建立非特异性静电相互作用,在蛋白p4结合区域的两端诱导弯曲。

相似文献

1
Bend induced by the phage phi 29 transcriptional activator in the viral late promoter is required for activation.噬菌体phi 29转录激活因子在病毒晚期启动子中诱导产生的弯曲对于激活是必需的。
J Mol Biol. 1990 Feb 20;211(4):713-25. doi: 10.1016/0022-2836(90)90072-t.
2
Short N-terminal deletions in the phage phi 29 transcriptional activator protein impair its DNA-binding ability.噬菌体phi 29转录激活蛋白的N端短缺失会损害其DNA结合能力。
Gene. 1990 Nov 30;96(1):75-81. doi: 10.1016/0378-1119(90)90343-p.
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Identification of the sequences recognized by phage phi 29 transcriptional activator: possible interaction between the activator and the RNA polymerase.噬菌体φ29转录激活因子识别序列的鉴定:激活因子与RNA聚合酶之间可能的相互作用。
Nucleic Acids Res. 1991 May 11;19(9):2337-42. doi: 10.1093/nar/19.9.2337.
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Characterization of a new prokaryotic transcriptional activator and its DNA recognition site.
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Transcription activation at a distance by phage phi 29 protein p4. Effect of bent and non-bent intervening DNA sequences.
J Mol Biol. 1991 Jun 5;219(3):403-14. doi: 10.1016/0022-2836(91)90182-6.
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Residues of the Bacillus subtilis phage phi 29 transcriptional activator required both to interact with RNA polymerase and to activate transcription.枯草芽孢杆菌噬菌体phi 29转录激活因子的残基既需要与RNA聚合酶相互作用,也需要激活转录。
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A DNA curvature can substitute phage phi 29 regulatory protein p4 when acting as a transcriptional repressor.当作为转录阻遏物起作用时,DNA弯曲可以替代噬菌体phi 29调节蛋白p4。
EMBO J. 1991 Nov;10(11):3429-38. doi: 10.1002/j.1460-2075.1991.tb04907.x.
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Bacteriophage PSP3 and phiR73 activator proteins: analysis of promoter specificities.噬菌体PSP3和phiR73激活蛋白:启动子特异性分析
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Transcriptional activator of phage phi 29 late promoter: mapping of residues involved in interaction with RNA polymerase and in DNA bending.噬菌体phi 29晚期启动子的转录激活因子:与RNA聚合酶相互作用及DNA弯曲相关残基的定位
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Transcription activation by phage phi29 protein p4 is mediated by interaction with the alpha subunit of Bacillus subtilis RNA polymerase.噬菌体phi29蛋白p4的转录激活是通过与枯草芽孢杆菌RNA聚合酶的α亚基相互作用介导的。
Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6616-20. doi: 10.1073/pnas.93.13.6616.

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A precise DNA bend angle is essential for the function of the phage phi29 transcriptional regulator.精确的DNA弯曲角度对于噬菌体phi29转录调节因子的功能至关重要。
Nucleic Acids Res. 2005 Jan 7;33(1):126-34. doi: 10.1093/nar/gki146. Print 2005.
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Binding of phage Phi29 architectural protein p6 to the viral genome: evidence for topological restriction of the phage linear DNA.噬菌体Phi29结构蛋白p6与病毒基因组的结合:噬菌体线性DNA拓扑限制的证据。
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Relevance of UP elements for three strong Bacillus subtilis phage phi29 promoters.UP元件对三个强枯草芽孢杆菌噬菌体phi29启动子的相关性
Nucleic Acids Res. 2004 Feb 18;32(3):1166-76. doi: 10.1093/nar/gkh290. Print 2004.
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The phi29 transcriptional regulator contacts the nucleoid protein p6 to organize a repression complex.phi29转录调节因子与类核蛋白p6相互作用以组建一个阻遏复合物。
EMBO J. 2002 Nov 15;21(22):6185-94. doi: 10.1093/emboj/cdf623.
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Mechanism for the switch of phi29 DNA early to late transcription by regulatory protein p4 and histone-like protein p6.调控蛋白p4和类组蛋白p6介导phi29 DNA转录从早期向晚期转换的机制。
EMBO J. 2001 Nov 1;20(21):6060-70. doi: 10.1093/emboj/20.21.6060.
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Transcription activation by phage phi29 protein p4 is mediated by interaction with the alpha subunit of Bacillus subtilis RNA polymerase.噬菌体phi29蛋白p4的转录激活是通过与枯草芽孢杆菌RNA聚合酶的α亚基相互作用介导的。
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