SINE transcription by RNA polymerase III is suppressed by histone methylation but not by DNA methylation

被引:76
作者
Varshney, Dhaval [1 ,2 ]
Vavrova-Anderson, Jana [1 ]
Oler, Andrew J. [3 ,4 ]
Cowling, Victoria H. [2 ]
Cairns, Bradley R. [3 ,4 ]
White, Robert J. [1 ,5 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Dundee, MRC Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland
[3] Univ Utah, Sch Med, Huntsman Canc Inst, Dept Oncol Sci, Salt Lake City, UT 84112 USA
[4] Univ Utah, Sch Med, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA
[5] Univ York, Dept Biol, York YO10 5DD, N Yorkshire, England
基金
英国惠康基金;
关键词
H3; LYSINE-9; METHYLATION; HOMOLOGOUS RECOMBINATION; ALU REPEATS; TANDEM DUPLICATION; POL II; BINDING; REPRESSION; CHROMATIN; ELEMENTS; MLL;
D O I
10.1038/ncomms7569
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
Short interspersed nuclear elements (SINEs), such as Alu, spread by retrotransposition, which requires their transcripts to be copied into DNA and then inserted into new chromosomal sites. This can lead to genetic damage through insertional mutagenesis and chromosomal rearrangements between non-allelic SINEs at distinct loci. SINE DNA is heavily methylated and this was thought to suppress its accessibility and transcription, thereby protecting against retrotransposition. Here we provide several lines of evidence that methylated SINE DNA is occupied by RNA polymerase III, including the use of high-throughput bisulphite sequencing of ChIP DNA. We find that loss of DNA methylation has little effect on accessibility of SINEs to transcription machinery or their expression in vivo. In contrast, a histone methyltransferase inhibitor selectively promotes SINE expression and occupancy by RNA polymerase III. The data suggest that methylation of histones rather than DNA plays a dominant role in suppressing SINE transcription.
引用
收藏
页数:12
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