体细胞突变
胞苷脱氨酶
生物
活化诱导(胞苷)脱氨酶
生发中心
亲和力成熟
体细胞
基因
遗传学
基底切除修复术
DNA错配修复
点突变
免疫球蛋白类转换
胞苷
分子生物学
B细胞
DNA修复
突变
抗体
生物化学
酶
作者
Jonathan U. Peled,Fei Kuang,Maria D. Iglesias-Ussel,Sergio Roa,Susan L. Kalis,Myron F. Goodman,Matthew D. Scharff
标识
DOI:10.1146/annurev.immunol.26.021607.090236
摘要
Affinity maturation of the humoral response is mediated by somatic hypermutation of the immunoglobulin (Ig) genes and selection of higher-affinity B cell clones. Activation-induced cytidine deaminase (AID) is the first of a complex series of proteins that introduce these point mutations into variable regions of the Ig genes. AID deaminates deoxycytidine residues in single-stranded DNA to deoxyuridines, which are then processed by DNA replication, base excision repair (BER), or mismatch repair (MMR). In germinal center B cells, MMR, BER, and other factors are diverted from their normal roles in preserving genomic integrity to increase diversity within the Ig locus. Both AID and these components of an emerging error-prone mutasome are regulated on many levels by complex mechanisms that are only beginning to be elucidated.
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