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噬菌体TP901-1的CI阻遏蛋白操纵位点的鉴定:与其他噬菌体的进化联系

Identification of operator sites of the CI repressor of phage TP901-1: evolutionary link to other phages.

作者信息

Johansen Annette H, Brøndsted Lone, Hammer Karin

机构信息

Section of Molecular Microbiology, Biocentrum-DTU, Technical University of Denmark, DK-2800, Lyngby, Denmark.

出版信息

Virology. 2003 Jun 20;311(1):144-56. doi: 10.1016/s0042-6822(03)00169-7.

Abstract

The repressor encoded by the cI gene of the temperate Lactococcus lactis subsp. cremoris bacteriophage TP901-1 has been purified. Gel-retardation and footprinting analyses identified three palindromic operator sites (O(R), O(L), and O(D)). The operator site O(R) is located between the two divergent early promoters P(R) and P(L), O(L) overlaps the transcriptional start of the lytic P(L) promoter, and O(D) is located downstream of the mor gene, the first gene in the lytic gene cluster. The function of O(L) was verified by mutational analysis. Binding was found to be specific and cooperative. Multimeric forms of the repressor were observed, thus indicating that the repressor may bind simultaneously to all three operator sites. Inverted repeats with homology to the operator sites of TP901-1 were identified in phage genomes encoding repressors homologous to CI of TP901-1. Interestingly, the locations of these repeats on the phage genomes correspond to those found in TP901-1, indicating that the same system of cooperative repression of early phage promoters has been inherited by modular evolution.

摘要

温和型乳酸乳球菌亚种cremoris噬菌体TP901-1的cI基因编码的阻遏蛋白已被纯化。凝胶阻滞和足迹分析确定了三个回文操纵位点(O(R)、O(L)和O(D))。操纵位点O(R)位于两个反向早期启动子P(R)和P(L)之间,O(L)与裂解性P(L)启动子的转录起始位点重叠,O(D)位于裂解基因簇中的第一个基因mor基因的下游。通过突变分析验证了O(L)的功能。发现结合具有特异性和协同性。观察到阻遏蛋白的多聚体形式,因此表明阻遏蛋白可能同时与所有三个操纵位点结合。在编码与TP901-1的CI同源的阻遏蛋白的噬菌体基因组中,鉴定出与TP901-1的操纵位点具有同源性的反向重复序列。有趣的是,这些重复序列在噬菌体基因组上的位置与在TP901-1中发现的位置相对应,这表明早期噬菌体启动子的协同阻遏系统通过模块进化得以遗传。

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