Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis

被引:174
作者
Ernst, Christina [1 ,2 ]
Eling, Nils [1 ,2 ]
Martinez-Jimenez, Celia P. [2 ,3 ]
Marioni, John C. [1 ,2 ,3 ]
Odom, Duncan T. [2 ,4 ]
机构
[1] European Bioinformat Inst, European Mol Biol Lab, Wellcome Genome Campus, Cambridge CB10 1SD, England
[2] Univ Cambridge, Canc Res UK Cambridge Inst, Robinson Way, Cambridge CB2 0RE, England
[3] Wellcome Sanger Inst, Welcome Genome Campus, Cambridge CB10 1SA, England
[4] German Canc Res Ctr, Div Signaling & Funct Genom, D-69120 Heidelberg, Germany
基金
英国惠康基金; 欧洲研究理事会;
关键词
MEIOTIC PROPHASE; GENE-EXPRESSION; SERTOLI-CELLS; STEM-CELLS; IN-SITU; TESTIS; ACID; SPERMIOGENESIS; SPERMATOGONIA; TRANSITIONS;
D O I
10.1038/s41467-019-09182-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Male gametes are generated through a specialised differentiation pathway involving a series of developmental transitions that are poorly characterised at the molecular level. Here, we use droplet-based single-cell RNA-Sequencing to profile spermatogenesis in adult animals and at multiple stages during juvenile development. By exploiting the first wave of spermatogenesis, we both precisely stage germ cell development and enrich for rare somatic cell-types and spermatogonia. To capture the full complexity of spermatogenesis including cells that have low transcriptional activity, we apply a statistical tool that identifies previously uncharacterised populations of leptotene and zygotene spermatocytes. Focusing on postmeiotic events, we characterise the temporal dynamics of X chromosome re-activation and profile the associated chromatin state using CUT&RUN. This identifies a set of genes strongly repressed by H3K9me3 in spermatocytes, which then undergo extensive chromatin remo-delling post-meiosis, thus acquiring an active chromatin state and spermatid-specific expression.
引用
收藏
页数:20
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