Transcription-coupled and epigenome-encoded mechanisms direct H3K4 methylation.
Transcription-coupled and epigenome-encoded mechanisms direct H3K4 methylation.
复制标题
转录偶联和表观基因组编码机制指导 H3K4 甲基化。
DOI:
10.1101/2021.06.03.446702
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Soichi Inagaki
中科院分区:
文献类型:
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作者:
Satoyo Oya;Mayumi Takahashi;Kazuya Takashima;Tetsuji Kakutani;Soichi Inagaki
Mono-, di-, and trimethylation of histone H3 lysine 4 (H3K4me1/2/3) are associated with transcription, yet it remains controversial whether H3K4me1/2/3 promote or result from transcription. Our previous characterizations ofArabidopsisH3K4 demethylases suggest roles for H3K4me1 in transcription. However, the control of H3K4me1 remains unexplored inArabidopsis, in which no methyltransferase for H3K4me1 has been identified. Here, we identify threeArabidopsismethyltransferases that direct H3K4me1. Analyses of their genome-wide localization using ChIP-seq and machine learning reveal that one of the enzymes cooperates with the transcription machinery, while the other two are associated with specific histone modifications and DNA sequences. Importantly, these two types of localization patterns are also found for the other H3K4 methyltransferases inArabidopsisand mice. These results suggest that H3K4me1/2/3 are established and maintained via interplay with transcription as well as inputs from other chromatin features, presumably enabling elaborate gene control.