Epigenetic Marking of the Zebrafish Developmental Program

被引:41
作者
Andersen, Ingrid S. [1 ,2 ]
Lindeman, Leif C. [1 ,2 ]
Reiner, Andrew H. [1 ,2 ]
Ostrup, Olga [1 ,2 ]
Aanes, Havard [3 ]
Alestrom, Peter [3 ]
Collas, Philippe [1 ,2 ]
机构
[1] Univ Oslo, Fac Med, Inst Basic Med Sci, Stem Cell Epigenet Lab, Oslo, Norway
[2] Univ Oslo, Norwegian Ctr Stem Cell Res, Oslo, Norway
[3] Norwegian Sch Vet Sci, BasAM, Oslo, Norway
来源
EPIGENETICS AND DEVELOPMENT | 2013年 / 104卷
关键词
PROMOTER DNA METHYLATION; EMBRYONIC-DEVELOPMENT; HISTONE MODIFICATIONS; GENOMIC METHYLATION; CHROMATIN-STRUCTURE; GENE-EXPRESSION; BINDING; ACTIVATION; TRANSCRIPTOME; IDENTIFICATION;
D O I
10.1016/B978-0-12-416027-9.00003-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A characteristic of anamniote development is a relatively long period of embryonic cell divisions in the absence of on-going transcription. In zebrafish, this period lasts for 10 cell cycles, or similar to 3-h postfertilization, after which zygotic genome activation (ZGA) takes place during the midblastula transition. How the embryo establishes transcriptional competence and how ZGA is spatially and temporally regulated have not been examined until recently. We review here recent data on the transitions in DNA methylation and posttranslational histone modifications occurring during early zebrafish development, as the embryo acquires transcriptional competence and initiates its own gene expression program. We also address models accounting for the origin of epigenetic states detected in early embryos. From these observations, a concept of epigenetic prepatterning of the embryonic gene expression program prior to the onset of ZGA is emerging. The recent data collectively start shedding light on how ZGA may be programmed and regulated.
引用
收藏
页码:85 / 112
页数:28
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