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N4病毒粒子RNA聚合酶转录起始位点。

N4 virion RNA polymerase sites of transcription initiation.

作者信息

Haynes L L, Rothman-Denes L B

出版信息

Cell. 1985 Jun;41(2):597-605. doi: 10.1016/s0092-8674(85)80032-5.

Abstract

Coliphage N4 virion encapsulated RNA polymerase shows a marked preference for denatured N4 DNA as a template. We show that initiation on denatured N4 virion DNA occurs with in vivo specificity. The location of the in vivo and in vitro initiation sites and the corresponding DNA sequences were determined. The N4 virion RNA polymerase promoters contain extensive sequence homology from position -18 to position 1, with a conserved GC-rich heptamer centered at -12, and two sets of short inverted repeats. We suggest that the N4 virion RNA polymerase recognizes the promoter only in a novel single-stranded form, and that the formation of the initiation complex is facilitated in vivo by supercoiling and E. coli single-stranded DNA binding protein.

摘要

大肠杆菌噬菌体N4病毒粒子包裹的RNA聚合酶对变性的N4 DNA作为模板表现出明显的偏好。我们发现,在变性的N4病毒粒子DNA上起始具有体内特异性。确定了体内和体外起始位点的位置以及相应的DNA序列。N4病毒粒子RNA聚合酶启动子从-18位到1位具有广泛的序列同源性,在-12位有一个保守的富含GC的七聚体,以及两组短的反向重复序列。我们认为,N4病毒粒子RNA聚合酶仅以一种新的单链形式识别启动子,并且在体内超螺旋和大肠杆菌单链DNA结合蛋白促进了起始复合物的形成。

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