Balganesh T S, Lacks S A
J Bacteriol. 1985 Jun;162(3):979-84. doi: 10.1128/jb.162.3.979-984.1985.
Mutations affecting heteroduplex DNA mismatch repair in Streptococcus pneumoniae were localized in two genes, hexA and hexB, by fractionation of restriction fragments carrying mutant alleles. A fragment containing the hexA4 allele was cloned in the S. pneumoniae cloning system, and the hexA+ allele was introduced into the recombinant plasmid by chromosomal facilitation of plasmid transfer. Subcloning localized the functional hexA gene to a 3.5-kilobase segment of the cloned pneumococcal DNA. The product of this gene was shown in Bacillus subtilis minicells to be a polypeptide with an Mr of 86,000. Two mutant alleles of hexA showed partial expression of the repair system when present in multicopy plasmids. A model for mismatch repair, which depends on the interaction of two protein components to recognize the mismatched base pair and excise a segment of DNA between strand breaks surrounding the mismatch, is proposed.
通过携带突变等位基因的限制性片段分级分离,将影响肺炎链球菌异源双链DNA错配修复的突变定位在两个基因hexA和hexB中。含有hexA4等位基因的片段被克隆到肺炎链球菌克隆系统中,通过质粒转移的染色体促进作用将hexA+等位基因导入重组质粒。亚克隆将功能性hexA基因定位到克隆的肺炎球菌DNA的一个3.5千碱基片段上。该基因的产物在枯草芽孢杆菌微小细胞中显示为一种分子量为86,000的多肽。hexA的两个突变等位基因在多拷贝质粒中存在时显示出修复系统的部分表达。提出了一种错配修复模型,该模型依赖于两种蛋白质成分的相互作用来识别错配碱基对并切除错配周围链断裂之间的一段DNA。