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地衣芽孢杆菌spoOH基因的完整DNA序列及调控区域

The complete DNA sequence and regulatory regions of the Bacillus licheniformis spoOH gene.

作者信息

Ramakrishna N, Dubnau E, Smith I

出版信息

Nucleic Acids Res. 1984 Feb 24;12(4):1779-90. doi: 10.1093/nar/12.4.1779.

Abstract

We have determined the sequence of a 1228 base-pair cloned DNA fragment from Bacillus licheniformis capable of specifically complementing mutations in the spoOH gene, which is required for the early stage of sporulation in B. subtilis. The sequence has only one long open reading frame consisting of 168 codons. In vivo and in vitro transcription mapping studies indicate the size of complementary RNA to be around 1 kb with the 5' initiation site at base 79 and the 3' termination site in the area of base 1138. This indicates the presence of a 5' untranslated RNA and a fairly long 3' extension. The promoter sequence of this gene is 5'TATAAT3' at -10, and 5'TTGACG3' at -35, a typical E. coli-like promoter sequence, and is transcribed in vitro specifically only by RNA polymerase containing delta 55 and not delta 37-containing holoenzyme.

摘要

我们已经确定了来自地衣芽孢杆菌的一个1228个碱基对的克隆DNA片段的序列,该片段能够特异性地互补枯草芽孢杆菌孢子形成早期所需的spoOH基因突变。该序列只有一个由168个密码子组成的长开放阅读框。体内和体外转录图谱研究表明,互补RNA的大小约为1 kb,5'起始位点在第79个碱基处,3'终止位点在第1138个碱基区域。这表明存在5'非翻译RNA和相当长的3'延伸。该基因的启动子序列在-10处为5'TATAAT3',在-35处为5'TTGACG3',是典型的大肠杆菌样启动子序列,并且在体外仅由含有δ55的RNA聚合酶特异性转录,而不是含有δ37的全酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01ff/318620/7ad34c12031a/nar00322-0026-a.jpg

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