Neuberger Michael S, Rada Cristina
Medical Research Council Laboratory of Molecular Biology, Cambridge, UK.
J Exp Med. 2007 Jan 22;204(1):7-10. doi: 10.1084/jem.20062409. Epub 2006 Dec 26.
Somatic hypermutation (SHM) introduces nucleotide substitutions into immunoglobulin variable (Ig V) region genes at all four bases, but the mutations at C/G and A/T pairs are achieved by distinct mechanisms. Mutations at C/G pairs are a direct consequence of the C-->U deamination catalyzed by activation-induced deaminase (AID). Mutations at A/T pairs, however, require a second mutagenic process that occurs during patch repair of the AID-generated U/G mismatch. Several DNA polymerases have been proposed to play a role in SHM, but accumulating evidence indicates that the mutations at A/T are overwhelmingly achieved by recruitment of DNA polymerase eta.
体细胞高频突变(SHM)会在免疫球蛋白可变区(Ig V)基因的所有四个碱基处引入核苷酸替换,但C/G和A/T碱基对处的突变是通过不同机制实现的。C/G碱基对处的突变是激活诱导脱氨酶(AID)催化C→U脱氨的直接结果。然而,A/T碱基对处的突变需要在修复AID产生的U/G错配的补丁修复过程中发生的第二个诱变过程。已经提出几种DNA聚合酶在SHM中起作用,但越来越多的证据表明,A/T处的突变绝大多数是通过招募DNA聚合酶η实现的。