An FGF timer for zygotic genome activation

被引:6
|
作者
Treen, Nicholas [1 ]
Chavarria, Emily [2 ]
Weaver, Claire J. [2 ]
Brangwynne, Clifford P. [1 ,3 ,4 ]
Levine, Michael [1 ,2 ]
机构
[1] Princeton Univ, Lewis Sigler Inst Integrat Genom, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[3] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[4] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
美国国家卫生研究院;
关键词
Ciona; developmental biology; zygotic genome activation; NEURAL TISSUE; TRANSCRIPTION; SPECIFICATION; REPRESSION; PROTEIN; EMBRYOS; FATE; ERF;
D O I
10.1101/gad.350164.122
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Zygotic genome activation has been extensively studied in a variety of systems including flies, frogs, and mammals. However, there is comparatively little known about the precise timing of gene induction during the earliest phases of embryogenesis. Here we used high-resolution in situ detection methods, along with genetic and experimental manipulations, to study the timing of zygotic activation in the simple model chordate Ciona with minute-scale temporal precision. We found that two Prdm1 homologs in Ciona are the earliest genes that respond to FGF signaling. We present evidence for a FGF timing mechanism that is driven by ERK-mediated derepression of the ERF repressor. Depletion of ERF results in ectopic activation of FGF target genes throughout the embryo. A highlight of this timer is the sharp transition in FGF responsiveness between the eight- and 16-cell stages of development. We propose that this timer is an innovation of chordates that is also used by vertebrates.
引用
收藏
页码:80 / 85
页数:6
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