Loenen W A, Daniel A S, Braymer H D, Murray N E
Department of Molecular Biology, University of Edinburgh, Scotland.
J Mol Biol. 1987 Nov 20;198(2):159-70. doi: 10.1016/0022-2836(87)90303-2.
The nucleotide sequence of the hsdR and M genes, together with that for hsdS comprises an 8400 base segment spanning the entire hsd region of Escherichia coli K-12. The three hsd genes are transcribed in the same direction, but from two promoters. hsdR and hsdM are separated by 492 base-pairs, whereas the termination codon of hsdM overlaps the initiation codon of hsdS. pres precedes hsdR, and our data indicate a transcription termination signal in the interval between hsdR and pmod, as expected if transcription of hsdM and S is dependent on pmod. Transcription from pres is not influenced by the products of the hsdM and S genes, and the mechanism whereby restriction is prevented when the hsd region is transferred to a modification-deficient cell remains to be elucidated. A segment of the predicted amino acid sequence of the M polypeptide shares homology with a variety of adenine methylases and may identify part of the active site for methylation of specific adenine residues. The R polypeptide shows homology with a variety of ATPases, and pronounced regions of alpha-helical structure are predicted, one of which is amphipathic.
hsdR和M基因的核苷酸序列,连同hsdS的序列,构成了一个跨越大肠杆菌K - 12整个hsd区域的8400个碱基的片段。这三个hsd基因沿相同方向转录,但来自两个启动子。hsdR和hsdM相隔492个碱基对,而hsdM的终止密码子与hsdS的起始密码子重叠。pres位于hsdR之前,我们的数据表明在hsdR和pmod之间的区间存在转录终止信号,正如预期的那样,如果hsdM和S的转录依赖于pmod。来自pres的转录不受hsdM和S基因产物的影响,当hsd区域转移到修饰缺陷型细胞时防止限制的机制仍有待阐明。M多肽预测的氨基酸序列的一段与多种腺嘌呤甲基化酶具有同源性,可能确定了特定腺嘌呤残基甲基化的活性位点的一部分。R多肽与多种ATP酶具有同源性,预测有明显的α - 螺旋结构区域,其中一个是两亲性的。