Molecular and Cell Biology, Taiwan International Graduate Program, Academia Sinica, Taipei 11529, Taiwan, R.O.C.
Graduate Institute of Life Science, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C.
Development. 2020 Jan 15;147(2):dev182063. doi: 10.1242/dev.182063.
WD40 proteins control many cellular processes via protein interactions. Wuho (Wh, a WD40 protein) controls fertility, although the involved mechanisms are unclear. Here, we show that Wh promotion of Mei-p26 (a human TRIM32 ortholog) function maintains ovarian germ cell homeostasis. Wh and Mei-p26 are epistatically linked, with and mutants showing nearly identical phenotypes, including germline stem cell (GSC) loss, stem-cyst formation due to incomplete cytokinesis between GSCs and daughter cells, and overproliferation of GSC progeny. Mechanistically, Wh interacts with Mei-p26 in different cellular contexts to induce cell type-specific effects. In GSCs, Wh and Mei-p26 promote BMP stemness signaling for proper GSC division and maintenance. In GSC progeny, Wh and Mei-p26 silence translation, downregulate a subset of microRNAs involved in germ cell differentiation and suppress ribosomal biogenesis via dMyc to limit germ cell mitosis. We also found that the human ortholog of Wh (WDR4) interacts with TRIM32 in human cells. Our results show that Wh is a regulator of Mei-p26 in germ cells and suggest that the WD40-TRIM interaction may also control tissue homeostasis in other stem cell systems.
WD40 蛋白通过蛋白相互作用控制许多细胞过程。Wuho(Wh,一种 WD40 蛋白)控制着生殖能力,尽管涉及的机制尚不清楚。在这里,我们表明 Wh 促进 Mei-p26(人类 TRIM32 同源物)的功能维持卵巢生殖细胞的稳态。Wh 和 Mei-p26 是上位性相关的,和 突变体表现出几乎相同的表型,包括生殖干细胞(GSC)丢失、由于 GSCs 和子细胞之间不完全胞质分裂而形成的干细胞囊肿,以及 GSC 后代的过度增殖。在机制上,Wh 在不同的细胞环境中与 Mei-p26 相互作用,诱导细胞类型特异性效应。在 GSCs 中,Wh 和 Mei-p26 促进 BMP 干性信号以进行适当的 GSC 分裂和维持。在 GSC 后代中,Wh 和 Mei-p26 沉默 翻译,下调一组参与生殖细胞分化的 microRNAs,并通过 dMyc 抑制核糖体生物发生,以限制生殖细胞有丝分裂。我们还发现 Wh 的人类同源物(WDR4)在人类细胞中与 TRIM32 相互作用。我们的结果表明 Wh 是 Mei-p26 在 生殖细胞中的调节剂,并表明 WD40-TRIM 相互作用可能也控制其他干细胞系统中的组织稳态。