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大肠杆菌uvrD基因调控区的核苷酸序列。

Nucleotide sequence of the regulatory region of the uvrD gene of Escherichia coli.

作者信息

Finch P, Emmerson P T

出版信息

Gene. 1983 Nov;25(2-3):317-23. doi: 10.1016/0378-1119(83)90236-6.

Abstract

We have sequenced the control region of the Escherichia coli uvrD gene and demonstrated the presence of a nucleotide sequence which is a perfect match for the consensus LexA protein binding site [Little and Mount, Cell 29 (1982) 11-22]. Upstream of this presumed LexA binding site is a promoter sequence, uvrD P1 which would be under LexA control while farther downstream is another possible promoter, uvrD P2, which would be independent of LexA control. Downstream of the LexA binding site is a potential transcription terminator in the form of a stem-loop structure followed by a series of T residues. On the basis of this sequence analysis, expression of the uvrD gene would be expected to increase after DNA damage or replication inhibition as part of the SOS response, as is reported in the preceding paper [Arthur and Eastlake, Gene 25 (1983) 309-316].

摘要

我们已对大肠杆菌uvrD基因的调控区进行了测序,并证明存在一个核苷酸序列,该序列与LexA蛋白结合位点的共有序列完全匹配[利特尔和芒特,《细胞》29(1982)11 - 22]。在这个推测的LexA结合位点上游是一个启动子序列uvrD P1,它将受LexA调控,而在更下游是另一个可能的启动子uvrD P2,它将独立于LexA调控。LexA结合位点下游是一个潜在的转录终止子,其形式为茎环结构,后面跟着一系列T残基。基于此序列分析,正如前文[亚瑟和伊斯特莱克,《基因》25(1983)309 - 316]所报道的,uvrD基因的表达预计会在DNA损伤或复制抑制后作为SOS反应的一部分而增加。

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