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阿维链霉菌A因子调控级联反应中的关键转录激活因子——AraC/XylS家族的AdpA的自抑制作用

Autorepression of AdpA of the AraC/XylS family, a key transcriptional activator in the A-factor regulatory cascade in Streptomyces griseus.

作者信息

Kato Jun-Ya, Ohnishi Yasuo, Horinouchi Sueharu

机构信息

Department of Biotechnology, Graduate School of Agriculture and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.

出版信息

J Mol Biol. 2005 Jul 1;350(1):12-26. doi: 10.1016/j.jmb.2005.04.058.

Abstract

AdpA belonging to the AraC/XylS family is a key transcriptional activator in the A-factor regulatory cascade in Streptomyces griseus, activating a number of genes required for physiological and morphological differentiation. On the other hand, AdpA repressed its own transcription by cooperative binding to the promoter region containing multiple operator sites. AdpA contained three operator sites, site 1 approximately at nucleotide position -100, site 2 at the promoter elements, and site 3 at position +80. AdpA bound to a strong binding site 1 increased the affinity for AdpA of a weak site 2, probably by forming a DNA loop via the two molecules of AdpA dimer, thus preventing RNA polymerase from access to the promoter. AdpA bound to site 3 with rather weak affinity repressed the AdpA promoter activity independently of sites 1 and 2, perhaps preventing RNA polymerase from chain elongation. Consistent with this model, the in vivo transcription of AdpA containing mutated site 1 or site 3 was greatly increased. In addition, streptomycin production, one of the phenotypes controlled positively by AdpA, was greatly increased in the mutants containing AdpA with a mutation at site 1 and site 3. The in vitro transcription of AdpA containing mutated site 1 was also increased. Thus, the transcription of AdpA, encoding an important transcriptional factor for ordered physiological and morphological development, is self-controlled.

摘要

属于AraC/XylS家族的AdpA是灰色链霉菌A因子调控级联反应中的关键转录激活因子,可激活生理和形态分化所需的多个基因。另一方面,AdpA通过与含有多个操纵位点的启动子区域协同结合来抑制自身转录。AdpA包含三个操纵位点,位点1大约在核苷酸位置-100处,位点2在启动子元件处,位点3在位置+80处。与强结合位点1结合的AdpA增加了与弱位点2的AdpA亲和力,可能是通过两个AdpA二聚体分子形成DNA环,从而阻止RNA聚合酶进入启动子。与位点3以相当弱的亲和力结合的AdpA独立于位点1和位点2抑制AdpA启动子活性,可能是阻止RNA聚合酶进行链延伸。与该模型一致,含有突变位点1或位点3的AdpA的体内转录大大增加。此外,在含有位点1和位点3发生突变的AdpA的突变体中,由AdpA正向控制的表型之一链霉素产量大大增加。含有突变位点1的AdpA的体外转录也增加。因此,编码有序生理和形态发育重要转录因子的AdpA的转录是自我调控的。

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