AID is required to initiate Nbs1/gamma-H2AX focus formation and mutations at sites of class switching

Article

关键词: DOUBLE-STRAND BREAKS;    CYTIDINE DEAMINASE AID;    HEAVY-CHAIN SWITCH;    SOMATIC HYPERMUTATION;    B-CELLS;    IMMUNOGLOBULIN GENES;    DNA-DAMAGE;    RECOMBINATION;    REPAIR;    SEQUENCES;   

DOI  :  10.1038/414660a

来源: SCIE

【 摘 要 】

Class switch recombination (CSR) is a region-specific DNA recombination reaction that replaces one immunoglobulin heavy-chain constant region (CH) gene with another. This enables a single variable (V) region gene to be used in conjunction with different downstream CH genes, each having a unique biological activity. The molecular mechanisms that mediate CSR have not been defined, but activation-induced cytidine deaminase (AID), a putative RNA-editing enzyme, is required for this reaction(1). Here we report that the Nijmegen breakage syndrome protein (Nbs1) and phosphorylated H2A histone family member X (gamma -H2AX, also known as gamma -H2afx), which facilitate DNA double-strand break (DSB) repair(2-4), form nuclear foci at the CH region in the G1 phase of the cell cycle in cells undergoing CSR, and that switching is impaired in H2AX(-/-) mice. Localization of Nbs1 and gamma -H2AX to the IgH locus during CSR is dependent on AID. In addition, AID is required for induction of switch region (S mu)-specific DNA lesions that precede CSR. These results place AID function upstream of the DNA modifications that initiate CSR.

【 授权许可】

Free