Distinct patterns of RNA polymerase II and transcriptional elongation characterize mammalian genome activation

被引:11
作者
Abe, Kenichiro [1 ]
Schauer, Tamas [1 ,2 ]
Torres-Padilla, Maria-Elena [1 ,3 ]
机构
[1] Helmholtz Zentrum Munchen, Inst Epigenet & Stem Cells, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Biomed Ctr, Bioinformat Unit, D-82152 Planegg Martinsried, Germany
[3] Ludwig Maximilians Univ Munchen, Fac Biol, Munich, Germany
来源
CELL REPORTS | 2022年 / 41卷 / 13期
关键词
GENE-EXPRESSION; IN-VIVO; MOUSE OOCYTES; MUERV-L; CHROMATIN; CELLS; SEQ; SPT5; DEGRADATION; TERMINATION;
D O I
10.1016/j.celrep.2022.111865
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
How transcription is regulated as development commences is fundamental to understand how the transcriptionally silent mature gametes are reprogrammed. The embryonic genome is activated for the first time during zygotic genome activation (ZGA). How RNA polymerase II (Pol II) and productive elongation are regulated during this process remains elusive. Here, we generate genome-wide maps of Serine 5 and Serine 2-phosphorylated Pol II during and after ZGA in mouse embryos. We find that both phosphorylated Pol II forms display similar distributions across genes during ZGA, with typical elongation enrichment of Pol II emerging after ZGA. Serine 2-phosphorylated Pol II occurs at genes prior to their activation, suggesting that Serine 2 phosphorylation may prime gene expression. Functional perturbations demonstrate that CDK9 and SPT5 are major ZGA regulators and that SPT5 prevents precocious activation of some genes. Overall, our work sheds molecular insights into transcriptional regulation at the beginning of mammalian development.
引用
收藏
页数:22
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