A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary

• Main Authors: Junker, Jan Philipp (Contributor), Gill, Mark E. (Contributor), Mueller, Jacob L. (Author), van Oudenaarden, Alexander (Contributor), Soh, Ying Qi Shirleen (Author), Page, David C (Author)
• Other Authors: Massachusetts Institute of Technology. Department of Biology (Contributor), Massachusetts Institute of Technology. Department of Physics (Contributor), Whitehead Institute for Biomedical Research (Contributor), Soh, Y. Q. Shirleen (Contributor), Page, David C. (Contributor)
• Format: Article
• Language: English
• Published: Public Library of Science, 2015-11-09T16:45:58Z.
• Subjects: Article
• Online Access: Get fulltext

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.
Howard Hughes Medical Institute
European Research Council (Grant ERC-AdG 294325-GeneNoiseControl)
National Institutes of Health (U.S.) (Grant R01-GM068957)
Howard Hughes Medical Institute (International Student Research Fellowship)
Whitehead Institute for Biomedical Research (Abraham Siegal Fellowship)