Priebe S D, Hadi S M, Greenberg B, Lacks S A
Biology Department, Brookhaven National Laboratory, Upton, New York 11973.
J Bacteriol. 1988 Jan;170(1):190-6. doi: 10.1128/jb.170.1.190-196.1988.
The Hex system of heteroduplex DNA base mismatch repair operates in Streptococcus pneumoniae after transformation and replication to correct donor and nascent DNA strands, respectively. A functionally similar system, called Mut, operates in Escherichia coli and Salmonella typhimurium. The nucleotide sequence of a 3.8-kilobase segment from the S. pneumoniae chromosome that includes the 2.7-kilobase hexA gene was determined. An open reading frame that could encode a 17-kilodalton polypeptide (OrfC) was located just upstream of the gene encoding a polypeptide of 95 kilodaltons corresponding to HexA. Shine-Dalgarno sequences and putative promoters were identified upstream of each protein start site. Insertion mutations showed that only HexA functioned in mismatch repair and that the promoter for hexA transcription was located within the OrfC-coding region. The HexA polypeptide contains a consensus sequence for ATP- or GTP-binding sites in proteins. Comparison of the entire HexA protein sequence to that of MutS of S. typhimurium, which was determined by Haber et al. in the accompanying paper (L. T. Haber, P. P. Pang, D. I. Sobell, J. A. Mankovitch, and G. C. Walker, J. Bacteriol. 170:197-202, 1988), showed the proteins to be homologous, inasmuch as 36% of their amino acid residues were identical. This homology indicates that the Hex and Mut systems of mismatch repair evolved from an ancestor common to the gram-positive streptococci and the gram-negative enterobacteria. It is the first direct evidence linking the two systems.
异源双链DNA碱基错配修复的Hex系统在肺炎链球菌转化和复制后发挥作用,分别校正供体DNA链和新生DNA链。一种功能类似的系统,称为Mut,在大肠杆菌和鼠伤寒沙门氏菌中发挥作用。测定了肺炎链球菌染色体上一个3.8千碱基片段的核苷酸序列,该片段包含2.7千碱基的hexA基因。一个可编码17千道尔顿多肽(OrfC)的开放阅读框位于编码与HexA相对应的95千道尔顿多肽的基因上游。在每个蛋白质起始位点上游鉴定出了Shine-Dalgarno序列和推定的启动子。插入突变表明,只有HexA在错配修复中起作用,hexA转录的启动子位于OrfC编码区内。HexA多肽包含蛋白质中ATP或GTP结合位点的共有序列。将整个HexA蛋白序列与鼠伤寒沙门氏菌的MutS蛋白序列进行比较(Haber等人在随附论文中测定了该序列[L.T.Haber,P.P.Pang,D.I.Sobell,J.A.Mankovitch,和G.C.Walker,J.Bacteriol.170:197 - 202,1988]),结果显示这两种蛋白质具有同源性,因为它们有36%的氨基酸残基相同。这种同源性表明,错配修复的Hex和Mut系统是从革兰氏阳性链球菌和革兰氏阴性肠杆菌的共同祖先进化而来的。这是将这两个系统联系起来的首个直接证据。