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Arac/XylS转录调节因子家族。

Arac/XylS family of transcriptional regulators.

作者信息

Gallegos M T, Schleif R, Bairoch A, Hofmann K, Ramos J L

机构信息

Department of Biochemistry and Molecular and Cellular Biology of Plants, Consejo Superior de Investigaciones Científicas, Estación Experimental del Zaìdín, Granada, Spain.

出版信息

Microbiol Mol Biol Rev. 1997 Dec;61(4):393-410. doi: 10.1128/mmbr.61.4.393-410.1997.

Abstract

The ArC/XylS family of prokaryotic positive transcriptional regulators includes more than 100 proteins and polypeptides derived from open reading frames translated from DNA sequences. Members of this family are widely distributed and have been found in the gamma subgroup of the proteobacteria, low- and high-G + C-content gram-positive bacteria, and cyanobacteria. These proteins are defined by a profile that can be accessed from PROSITE PS01124. Members of the family are about 300 amino acids long and have three main regulatory functions in common: carbon metabolism, stress response, and pathogenesis. Multiple alignments of the proteins of the family define a conserved stretch of 99 amino acids usually located at the C-terminal region of the regulator and connected to a nonconserved region via a linker. The conserved stretch contains all the elements required to bind DNA target sequences and to activate transcription from cognate promoters. Secondary analysis of the conserved region suggests that it contains two potential alpha-helix-turn-alpha-helix DNA binding motifs. The first, and better-fitting motif is supported by biochemical data, whereas existing biochemical data neither support nor refute the proposal that the second region possesses this structure. The phylogenetic relationship suggests that members of the family have recruited the nonconserved domain(s) into a series of existing domains involved in DNA recognition and transcription stimulation and that this recruited domain governs the role that the regulator carries out. For some regulators, it has been demonstrated that the nonconserved region contains the dimerization domain. For the regulators involved in carbon metabolism, the effector binding determinants are also in this region. Most regulators belonging to the AraC/XylS family recognize multiple binding sites in the regulated promoters. One of the motifs usually overlaps or is adjacent to the -35 region of the cognate promoters. Footprinting assays have suggested that these regulators protect a stretch of up to 20 bp in the target promoters, and multiple alignments of binding sites for a number of regulators have shown that the proteins recognize short motifs within the protected region.

摘要

原核生物正转录调节因子的ArC/XylS家族包括100多种蛋白质和多肽,它们来源于从DNA序列翻译而来的开放阅读框。该家族成员分布广泛,已在变形菌门的γ亚群、低G+C含量和高G+C含量的革兰氏阳性菌以及蓝细菌中发现。这些蛋白质由一个可从PROSITE PS01124获取的图谱定义。该家族成员约300个氨基酸长,具有三个共同的主要调节功能:碳代谢、应激反应和致病作用。该家族蛋白质的多重比对确定了一段99个氨基酸的保守序列,通常位于调节因子的C末端区域,并通过一个连接子与一个非保守区域相连。保守序列包含结合DNA靶序列和激活同源启动子转录所需的所有元件。对保守区域的二级分析表明,它包含两个潜在的α-螺旋-转角-α-螺旋DNA结合基序。第一个且拟合度更好的基序得到了生化数据的支持,而现有的生化数据既不支持也不反驳第二个区域具有这种结构的提议。系统发育关系表明,该家族成员已将非保守结构域纳入一系列参与DNA识别和转录刺激的现有结构域中,并且这种招募的结构域决定了调节因子所发挥的作用。对于一些调节因子,已证明非保守区域包含二聚化结构域。对于参与碳代谢的调节因子,效应物结合决定簇也在该区域。大多数属于AraC/XylS家族的调节因子识别受调控启动子中的多个结合位点。其中一个基序通常与同源启动子的-35区域重叠或相邻。足迹分析表明,这些调节因子在靶启动子中保护一段长达20 bp的序列,并且多个调节因子结合位点的比对表明,这些蛋白质识别受保护区域内的短基序。

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本文引用的文献

1
L-Arabinose-sensitive, L-ribulose 5-phosphate 4-epimerase-deficient mutants of Escherichia coli.
J Bacteriol. 1962 Jul;84(1):137-46. doi: 10.1128/jb.84.1.137-146.1962.
2
Structural basis for ligand-regulated oligomerization of AraC.
Science. 1997 Apr 18;276(5311):421-5. doi: 10.1126/science.276.5311.421.
4
How AraC interacts specifically with its target DNAs.
J Mol Biol. 1996 Dec 13;264(4):667-74. doi: 10.1006/jmbi.1996.0668.
6
The linker region of AraC protein.
J Bacteriol. 1996 Dec;178(24):7025-30. doi: 10.1128/jb.178.24.7025-7030.1996.
8
YbtA, an AraC-type regulator of the Yersinia pestis pesticin/yersiniabactin receptor.
Mol Microbiol. 1996 Oct;22(2):315-25. doi: 10.1046/j.1365-2958.1996.00118.x.
10
Dual regulation of the paraquat-inducible gene pqi-5 by SoxS and RpoS in Escherichia coli.
Mol Microbiol. 1996 Oct;22(1):53-61. doi: 10.1111/j.1365-2958.1996.tb02655.x.

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