Bucci C, Lavitola A, Salvatore P, Del Giudice L, Massardo D R, Bruni C B, Alifano P
Dipartimento di Biologia e Patologia, Cellulare e Molecolare, L. Califano, Università di Napoli Federico II, Centro di Endocrinologia ed Oncologia Sperimentale G. Salvatore of the Consiglio Nazionale delle Ricerche, Italy.
Mol Cell. 1999 Apr;3(4):435-45. doi: 10.1016/s1097-2765(00)80471-2.
Expression of serogroup B meningococcal capsular polysaccharide undergoes frequent phase variation involving reversible frameshift mutations within a homopolymeric repeat in the siaD gene. A high rate of phase variation is the consequence of a biochemical defect in methyl-directed mismatch repair. The mutator phenotype is associated to the absence of DNA adenine methyltransferase (Dam) activity in all pathogenic isolates and in 50% of commensal strains. Analysis of the meningococcal dam gene region revealed that in all Dam- strains a gene encoding a putative restriction endonuclease (drg) that cleaves only the methylated DNA sequence 5'-GmeATC-3' replaced the dam gene. Insertional inactivation of the dam and/or drg genes indicated that high rates of phase variation and hypermutator phenotype are caused by absence of a functional dam gene.
B群脑膜炎球菌荚膜多糖的表达频繁发生相变,涉及siaD基因中一个同聚物重复序列内的可逆移码突变。高频率的相变是甲基定向错配修复中生化缺陷的结果。突变体表型与所有致病分离株和50%的共生菌株中缺乏DNA腺嘌呤甲基转移酶(Dam)活性有关。对脑膜炎球菌dam基因区域的分析表明,在所有Dam-菌株中,一个编码仅切割甲基化DNA序列5'-GmeATC-3'的推定限制性内切酶(drg)的基因取代了dam基因。dam和/或drg基因的插入失活表明,高频率的相变和超突变体表型是由功能性dam基因的缺失引起的。