Cromie Gareth A
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.
J Bacteriol. 2009 Aug;191(16):5076-84. doi: 10.1128/JB.00254-09. Epub 2009 Jun 19.
RecBCD and AddAB are bacterial enzymes that share similar helicase and nuclease activities and initiate repair of DNA double-strand breaks by homologous recombination. Examination of the phylogenetic distribution of AddAB and RecBCD revealed that one or the other complex is present in most sequenced bacteria. In addition, horizontal gene transfer (HGT) events involving addAB and recBCD appear to be common, with the genes encoding one complex frequently replacing those encoding the other. HGT may also explain the unexpected identification of archaeal addAB genes. More than 85% of addAB and recBCD genes are clustered on the genome, suggesting operon structures. A few organisms, including the Mycobacteria, encode multiple copies of these complexes of either the same or mixed classes. The possibility that the enzymatic activities of the AddAB and RecBCD enzymes promote their horizontal transfer is discussed, and the distribution of AddAB/RecBCD is compared to that of the RecU/RuvC resolvases. Finally, it appears that two sequence motifs, the Walker A box involved in ATP binding and an iron-sulfur-cysteine cluster, are present only in subsets of AddB proteins, suggesting the existence of mechanistically distinct classes of AddB.
RecBCD和AddAB是细菌酶,它们具有相似的解旋酶和核酸酶活性,并通过同源重组启动DNA双链断裂的修复。对AddAB和RecBCD的系统发育分布进行研究后发现,在大多数已测序的细菌中都存在这两种复合物中的一种。此外,涉及addAB和recBCD的水平基因转移(HGT)事件似乎很常见,编码一种复合物的基因经常取代编码另一种复合物的基因。HGT也可能解释了古菌addAB基因的意外发现。超过85%的addAB和recBCD基因在基因组上成簇分布,表明存在操纵子结构。包括分枝杆菌在内的一些生物体编码这些相同或混合类型复合物的多个拷贝。文中讨论了AddAB和RecBCD酶的酶活性促进其水平转移的可能性,并将AddAB/RecBCD的分布与RecU/RuvC解离酶的分布进行了比较。最后,似乎有两个序列基序,即参与ATP结合的沃克A框和一个铁硫半胱氨酸簇,仅存在于AddB蛋白的子集中,这表明存在机制上不同类型的AddB。