Histone3 lysine4 trimethylation regulated by the facilitates chromatin transcription complex is critical for DNA cleavage in class switch recombination

被引:78
作者
Stanlie, Andre [1 ]
Aida, Masatoshi [1 ]
Muramatsu, Masamichi [2 ]
Honjo, Tasuku [1 ]
Begum, Nasim A. [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Immunol & Genom Med, Kyoto 6068501, Japan
[2] Kanazawa Univ, Grad Sch Med Sci, Dept Mol Genet, Kanazawa, Ishikawa 9208640, Japan
关键词
RNA-POLYMERASE-II; CYTIDINE DEAMINASE AID; MEIOTIC RECOMBINATION; NUCLEOSOME DYNAMICS; V(D)J RECOMBINATION; H3K4; METHYLATION; ACTIVATION; UBIQUITYLATION; ELONGATION; INITIATION;
D O I
10.1073/pnas.1016923108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ig class switch recombination (CSR) requires expression of activation-induced cytidine deaminase (AID) and transcription through target switch (S) regions. Here we show that knockdown of the histone chaperone facilitates chromatin transcription (FACT) completely inhibited S region cleavage and CSR in IgA-switch-inducible CH12F3-2A B cells. FACT knockdown did not reduce AID or S region transcripts but did decrease histone3 lysine4 trimethylation (H3K4me3) at both the S mu and S alpha regions. Because knockdown of FACT or H3K4 methyltransferase cofactors inhibited DNA cleavage in H3K4me3-depleted S regions, H3K4me3 may serve as a mark for recruiting CSR recombinase. These findings revealed an unexpected evolutionary conservation between CSR and meiotic recombination.
引用
收藏
页码:22190 / 22195
页数:6
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