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Chromatin Accessibility Landscape in Human Early Embryos and Its Association with Evolution
Author(s) -
Lei Gao,
Keliang Wu,
Zhenbo Liu,
Xuelong Yao,
Shenli Yuan,
Wenrong Tao,
Lizhi Yi,
Guanling Yu,
Zhenzhen Hou,
Dongdong Fan,
Yong Tian,
Jianqiao Liu,
ZiJiang Chen,
Jiang Liu
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.02.028
Subject(s) - biology , maternal to zygotic transition , chromatin , transposable element , embryo , gene , genome , genetics , embryonic stem cell , embryogenesis , regulation of gene expression , promoter , microbiology and biotechnology , evolutionary biology , gene expression , zygote
The dynamics of the chromatin regulatory landscape during human early embryogenesis remains unknown. Using DNase I hypersensitive site (DHS) sequencing, we report that the chromatin accessibility landscape is gradually established during human early embryogenesis. Interestingly, the DHSs with OCT4 binding motifs are enriched at the timing of zygotic genome activation (ZGA) in humans, but not in mice. Consistently, OCT4 contributes to ZGA in humans, but not in mice. We further find that lower CpG promoters usually establish DHSs at later stages. Similarly, younger genes tend to establish promoter DHSs and are expressed at later embryonic stages, while older genes exhibit these features at earlier stages. Moreover, our data show that human active transposons SVA and HERV-K harbor DHSs and are highly expressed in early embryos, but not in differentiated tissues. In summary, our data provide an evolutionary developmental view for understanding the regulation of gene and transposon expression.

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