Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS, USA.
Nat Commun. 2021 Mar 19;12(1):1758. doi: 10.1038/s41467-021-22021-6.
The molecular machinery and chromosome structures carrying out meiosis are frequently conserved from yeast to mammals. However, signals initiating meiosis appear divergent: while nutrient restriction induces meiosis in the yeast system, retinoic acid (RA) and its target Stra8 have been shown to be necessary but not sufficient to induce meiotic initiation in mammalian germ cells. Here, we use primary culture of mouse undifferentiated spermatogonia without the support of gonadal somatic cells to show that nutrient restriction in combination with RA is sufficient to induce Stra8- and Spo11-dependent meiotic gene and chromosome programs that recapitulate the transcriptomic and cytologic features of in vivo meiosis. We demonstrate that neither nutrient restriction nor RA alone exerts these effects. Moreover, we identify a distinctive network of 11 nutrient restriction-upregulated transcription factor genes, which are associated with early meiosis in vivo and whose expression does not require RA. Our study proposes a conserved model, in which nutrient restriction induces meiotic initiation by upregulating key transcription factor genes for the meiotic gene program and provides an in vitro platform for meiotic induction that could facilitate research and haploid gamete production.
执行减数分裂的分子机制和染色体结构在从酵母到哺乳动物的过程中经常被保守。然而,启动减数分裂的信号似乎存在分歧:虽然营养限制会诱导酵母系统中的减数分裂,但已经表明视黄酸(RA)及其靶标 Stra8 对于诱导哺乳动物生殖细胞的减数分裂起始是必要的,但不是充分的。在这里,我们使用没有性腺体细胞支持的未分化精原细胞的原代培养,表明 RA 与营养限制相结合足以诱导 Stra8 和 Spo11 依赖性减数分裂基因和染色体程序,这些程序再现了体内减数分裂的转录组和细胞学特征。我们证明,单独的营养限制或 RA 都不会产生这些影响。此外,我们鉴定了一个独特的 11 个营养限制上调转录因子基因网络,这些基因与体内早期减数分裂有关,其表达不需要 RA。我们的研究提出了一个保守的模型,其中营养限制通过上调关键转录因子基因来诱导减数分裂起始,这些基因与减数分裂基因程序有关,并为减数分裂诱导提供了一个体外平台,这可能有助于研究和单倍体配子的产生。