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胎儿卵巢减数分裂前期的基因调控程序。

A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary.

作者信息

Soh Y Q Shirleen, Junker Jan Philipp, Gill Mark E, Mueller Jacob L, van Oudenaarden Alexander, Page David C

机构信息

Whitehead Institute, Cambridge, Massachusetts, United States of America; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.

Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America; Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America; Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences) Utrecht, Netherlands; University Medical Center Utrecht, Utrecht, Netherlands.

出版信息

PLoS Genet. 2015 Sep 17;11(9):e1005531. doi: 10.1371/journal.pgen.1005531. eCollection 2015 Sep.

Abstract

The chromosomal program of meiotic prophase, comprising events such as laying down of meiotic cohesins, synapsis between homologs, and homologous recombination, must be preceded and enabled by the regulated induction of meiotic prophase genes. This gene regulatory program is poorly understood, particularly in organisms with a segregated germline. We characterized the gene regulatory program of meiotic prophase as it occurs in the mouse fetal ovary. By profiling gene expression in the mouse fetal ovary in mutants with whole tissue and single-cell techniques, we identified 104 genes expressed specifically in pre-meiotic to pachytene germ cells. We characterized the regulation of these genes by 1) retinoic acid (RA), which induces meiosis, 2) Dazl, which is required for germ cell competence to respond to RA, and 3) Stra8, a downstream target of RA required for the chromosomal program of meiotic prophase. Initial induction of practically all identified meiotic prophase genes requires Dazl. In the presence of Dazl, RA induces at least two pathways: one Stra8-independent, and one Stra8-dependent. Genes vary in their induction by Stra8, spanning fully Stra8-independent, partially Stra8-independent, and fully Stra8-dependent. Thus, Stra8 regulates the entirety of the chromosomal program but plays a more nuanced role in governing the gene expression program. We propose that Stra8-independent gene expression enables the stockpiling of selected meiotic structural proteins prior to the commencement of the chromosomal program. Unexpectedly, we discovered that Stra8 is required for prompt down-regulation of itself and Rec8. Germ cells that have expressed and down-regulated Stra8 are refractory to further Stra8 expression. Negative feedback of Stra8, and subsequent resistance to further Stra8 expression, may ensure a single, restricted pulse of Stra8 expression. Collectively, our findings reveal a gene regulatory logic by which germ cells prepare for the chromosomal program of meiotic prophase, and ensure that it is induced only once.

摘要

减数分裂前期的染色体程序,包括诸如减数分裂黏连蛋白的形成、同源染色体配对和同源重组等事件,必须在减数分裂前期基因的调控诱导之前发生并由其促成。这个基因调控程序目前还知之甚少,尤其是在具有分离生殖系的生物体中。我们对小鼠胎儿卵巢中发生的减数分裂前期的基因调控程序进行了表征。通过使用全组织和单细胞技术对小鼠胎儿卵巢中的基因表达进行分析,我们鉴定出了104个在减数分裂前到粗线期生殖细胞中特异性表达的基因。我们通过以下三个方面对这些基因的调控进行了表征:1)诱导减数分裂的视黄酸(RA);2)生殖细胞对RA作出反应所必需的Dazl;3)减数分裂前期染色体程序所需的RA下游靶点Stra8。几乎所有已鉴定的减数分裂前期基因的初始诱导都需要Dazl。在有Dazl的情况下,RA至少诱导两条途径:一条不依赖Stra8,一条依赖Stra8。不同基因对Stra8诱导的反应各不相同,包括完全不依赖Stra8、部分不依赖Stra8和完全依赖Stra8。因此,Stra8调节整个染色体程序,但在控制基因表达程序中发挥着更为细微的作用。我们提出,不依赖Stra8的基因表达能够在染色体程序开始之前储存选定的减数分裂结构蛋白。出乎意料的是,我们发现Stra8对于自身和Rec8的迅速下调是必需的。已经表达并下调了Stra8的生殖细胞对进一步的Stra8表达具有抗性。Stra8的负反馈以及随后对进一步Stra8表达的抗性,可能确保了Stra8表达的单一、有限脉冲。总的来说,我们的研究结果揭示了一种基因调控逻辑,通过这种逻辑生殖细胞为减数分裂前期的染色体程序做好准备,并确保其只被诱导一次。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/175b/4574967/ec9bd83f484f/pgen.1005531.g001.jpg

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