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通过足迹法和核酸外切酶III分析对噬菌体S13的H/A基因区域中的RNA聚合酶结合位点进行定位。

Mapping of RNA polymerase binding sites in the H/A gene region of bacteriophage S13 by footprinting and exonuclease III analysis.

作者信息

Arquint M, Spencer J H

机构信息

Department of Biochemistry, Queen's University, Kingston, Ontario, Canada.

出版信息

Biochim Biophys Acta. 1994 Aug 2;1218(3):339-45. doi: 10.1016/0167-4781(94)90186-4.

Abstract

The H/A gene region of the bacteriophage S13 genome (map positions 4597 to 289) was analyzed for Escherichia coli RNA polymerase-binding sites by combined DNase I footprinting, exonuclease III analysis and DNA sequencing. Two high-affinity binding sites were identified, one corresponding to the A gene promoter at position 5384 to 56, overlapping the H/A intergenic region at position 1 to 63, the other at position 5171 to 5230, at the 3'-end of the H gene. A medium-affinity RNA polymerase binding site was mapped at position 4810 to 4850 in the middle of the H gene upstream of a low-affinity site at position 5280 to 5330. The studies complete footprinting analyses of the S13 genome from position 4597 to 2198 and in combination with previous studies on transcription provide definitive evidence on the position of the A gene promoter in S13 and the closely related phage psi X174.

摘要

通过结合DNA酶I足迹法、核酸外切酶III分析和DNA测序,对噬菌体S13基因组的H/A基因区域(图谱位置4597至289)进行了大肠杆菌RNA聚合酶结合位点分析。鉴定出两个高亲和力结合位点,一个对应于位置5384至56处的A基因启动子,与位置1至63处的H/A基因间隔区重叠,另一个位于H基因3'端的位置5171至5230处。在H基因中部位置4810至4850处定位到一个中等亲和力的RNA聚合酶结合位点,其上游位置5280至5330处为低亲和力位点。这些研究完成了对S13基因组从位置4597至2198的足迹分析,并结合先前关于转录的研究,为S13和密切相关的噬菌体psi X174中A基因启动子的位置提供了确凿证据。

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