Germ cell differentiation requires Tdrd7-dependent chromatin and transcriptome reprogramming marked by germ plasm relocalization.
Germ cell differentiation requires Tdrd7-dependent chromatin and transcriptome reprogramming marked by germ plasm relocalization.
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DOI:
10.1016/j.devcel.2021.02.007
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发表时间:
2021-03-08
影响因子:
11.8
通讯作者:
Müller F
中科院分区:
文献类型:
--
作者:
D'Orazio FM;Balwierz PJ;González AJ;Guo Y;Hernández-Rodríguez B;Wheatley L;Jasiulewicz A;Hadzhiev Y;Vaquerizas JM;Cairns B;Lenhard B;Müller F
In many animal models, primordial germ cell (PGC) development depends on maternally deposited germ plasm, which prevents somatic cell fate. Here, we show that PGCs respond to regulatory information from the germ plasm in two distinct phases using two distinct mechanisms in zebrafish. We demonstrate that PGCs commence zygotic genome activation together with the somatic blastocysts with no demonstrable differences in transcriptional and chromatin opening. Unexpectedly, both PGC and somatic blastocysts activate germ-cell-specific genes, which are only stabilized in PGCs by cytoplasmic germ plasm determinants. Disaggregated perinuclear relocalization of germ plasm during PGC migration is regulated by the germ plasm determinant Tdrd7 and is coupled to dramatic divergence between PGC and somatic transcriptomes. This transcriptional divergence relies on PGC-specific cis-regulatory elements characterized by promoter-proximal distribution. We show that Tdrd7-dependent reconfiguration of chromatin accessibility is required for elaboration of PGC fate but not for PGC migration. No evidence for transcriptional activation delay in zebrafish PGCs Germ-plasm-associated post-transcriptional divergence during ZGA Epigenetic reprogramming marks onset of PGC migration Epigenetic reprogramming in PGCs relies on Tdrd7, coupled to germ plasm relocalization D’Orazio et al. show that zygotic genome activation in zebrafish primordial germ cells (PGCs) occurs in two phases. PGCs and somatic cells activate the genome concurrently, showing similar transcriptional and chromatin landscapes. Divergence occurs during PGC migration, when a PGC-specific chromatin landscape is coupled to Tdrd7a-dependent perinuclear germ plasm relocalization.
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