首页> 美国卫生研究院文献>The EMBO Journal >Region 2.5 of the Escherichia coli RNA polymerase sigma70 subunit is responsible for the recognition of the extended-10 motif at promoters.
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Region 2.5 of the Escherichia coli RNA polymerase sigma70 subunit is responsible for the recognition of the extended-10 motif at promoters.

机译:大肠杆菌RNA聚合酶sigma70亚基的2.5区负责启动子上 extended-10基序的识别。

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摘要

At some bacterial promoters, a 5'-TG-3' sequence element, located one base upstream of the -10 hexamer element, provides an essential motif necessary for transcription initiation. We have identified a mutant of the Escherichia coli RNA polymerase sigma70 subunit that has an altered preference for base sequences in this 'extended -10' region. We show that this mutant sigma70 subunit substantially increases transcription from promoters bearing 5'-TC-3' or 5'-TT-3' instead of a 5'-TG-3' motif, located one base upstream of the -10 hexamer. The mutant results from a single base pair substitution in the rpoD gene that causes a Glu to Gly change at position 458 of sigma70. This substitution identifies a functional region in sigma70 that is immediately adjacent to the well-characterized region 2.4 (positions 434-453, previously shown to contact the -10 hexamer). From these results, we conclude that this region (which we name region 2.5) is involved in contacting the 5'-TG-3' motif found at some bacterial promoters: thus, extended -10 regions are recognized by an extended region 2 of the RNA polymerase sigma70 subunit.
机译:在某些细菌启动子上,位于-10六聚体元件上游一个碱基处的5'-TG-3'序列元件提供了转录起始所必需的必要基序。我们已经鉴定出大肠杆菌RNA聚合酶sigma70亚基的突变体,该突变体对该“扩展-10”区域中碱基序列的偏好有所改变。我们表明,此突变体sigma70亚基大大增加了从承载5'-TC-3'或5'-TT-3'而不是位于-10六聚体上游一个碱基的5'-TG-3'的启动子的转录。该突变体是由rpoD基因中的单个碱基对取代引起的,该取代导致sigma70位置458处的Glu变为Gly。该取代标识了sigma70中与功能齐全的区域2.4紧邻的功能区域(位置434-453,先前显示与-10六聚体接触)。根据这些结果,我们得出结论,该区域(我们将其称为区域2.5)与一些细菌启动子上的5'-TG-3'基序接触有关:因此,扩展的-10个区域可被细菌的扩展区域2识别。 RNA聚合酶sigma70亚基。

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