Conservation of regulatory elements controlling the expression of the rpsB-tsf operon in γ-proteobacteria

被引:10
作者
Aseev, L. V. [1 ]
Levandovskaya, A. A. [1 ]
Skaptsova, N. V. [1 ]
Boni, I. V. [1 ]
机构
[1] Russian Acad Sci, Shemyakin & Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
基金
俄罗斯基础研究基金会;
关键词
rpsB-tsf operon; gamma-proteobacteria; autogenous regulation; extended-10; promoter; phylogenetic analysis; ESCHERICHIA-COLI; PROTEIN-SYNTHESIS; RNA-POLYMERASE; PROMOTER; INITIATION; TRANSCRIPTION; RECOGNITION; SEQUENCE; REGION;
D O I
10.1134/S0026893309010142
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In eubacteria, the rpsB-tsf operon encodes two essential components of the translational apparatus, ribosomal protein S2 and elongation factor Ts. We have recently localized the promoter region of the Escherichia coli rpsB-tsf operon and have demonstrated that both rpsB and tsf are negatively regulated by S2 at the translational level. In this work, phylogenetic analysis showed high conservation of both the promoter signature and the structure of the 5'-untranslated region (5'-UTR) of the rpsB mRNA in gamma-proteobacteria. Despite the difference in length and overall primary structure of rpsB 5'-UTRs among various gamma-proteobacteria, several short regions within 5'-UTRs proved to be universally conserved, implying their participation in expression regulation. Phylogenetic predictions were experimentally verified. The putative rpsB promoter regions of Yersinia pestis, Haemophilus influenzae, and Pseudomonas aeruginosa drove transcription of the lacZ reporter in E. coli, and the corresponding rpsB 5'-UTRs were subject to autogenous repression by S2 in vivo.
引用
收藏
页码:101 / 107
页数:7
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