A basal promoter element recognized by free RNA polymerase σ subunit determines promoter recognition by RNA polymerase holoenzyme

被引:74
作者
Feklistov, Andrey
Barinova, Nataliya
Sevostyanova, Anastasiya
Heyduk, Ewa
Bass, Irina
Vvedenskaya, Irina
Kuznedelov, Konstantin
Merkiene, Egle
Stavrovskaya, Elena
Klimasauskas, Saulius
Nikiforov, Vadim
Heyduk, Tomasz
Severinov, Konstantin
Kulbachinskiy, Andrey
机构
[1] Russian Acad Sci, Inst Mol Genet, Moscow 123182, Russia
[2] Moscow MV Lomonosov State Univ, Dept Mol Biol, Moscow 119992, Russia
[3] Publ Hlth Res Inst, Newark, NJ 07103 USA
[4] St Louis Univ, Sch Med, St Louis, MO 63104 USA
[5] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
[6] Inst Biotechnol, LT-02241 Vilnius, Lithuania
[7] Russian Acad Sci, Inst Informat Transmiss Problems, Moscow 127994, Russia
关键词
D O I
10.1016/j.molcel.2006.06.010
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
During transcription initiation by bacterial RNA polymerase, the sigma subunit recognizes the -35 and -10 promoter elements; free sigma, however, does not bind DNA. We selected ssDNA aptamers that strongly and specifically bound free sigma(A) from Thermus aquaticus. A consensus sequence, GTA(CfT)AATGGGA, was required for aptamer binding to sigma(A), with the TA(C/T)AAT segment making interactions similar to those made by the -10 promoter element (consensus sequence TATAAT) in the context of RNA polymerase holoenzyme. When in dsDNA form, the aptamers function as strong promoters for the T. aquaticus RNA polymerase sigma(A) holoenzyme. Recognition of the aptamer-based promoters depends on the downstream GGGA motif from the aptamers' common sequence, which is contacted by sigma(A) region 1.2 and directs transcription initiation even in the absence of the -35 promoter element. Thus, recognition of bacterial promoters is controlled by independent interactions of a with multiple basal promoter elements.
引用
收藏
页码:97 / 107
页数:11
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