University at Albany, Department of Biological Sciences, RNA Institute; 1400 Washington Avenue, LSRB 2033D, Albany, NY 12222.
University at Albany, Department of Biological Sciences, RNA Institute; 1400 Washington Avenue, LSRB 2033D, Albany, NY 12222; 10x Genomics, Inc., 6230 Stoneridge Mall Road, Pleasanton, CA, 94588.
Curr Biol. 2021 Jul 26;31(14):2984-2994.e7. doi: 10.1016/j.cub.2021.04.052. Epub 2021 May 13.
In sexually reproducing animals, the oocyte contributes a large supply of RNAs that are essential to launch development upon fertilization. The mechanisms that regulate the composition of the maternal RNA contribution during oogenesis are unclear. Here, we show that a subset of RNAs expressed during the early stages of oogenesis is subjected to regulated degradation during oocyte specification. Failure to remove these RNAs results in oocyte dysfunction and death. We identify the RNA-degrading Super Killer complex and No-Go Decay factor Pelota as key regulators of oogenesis via targeted degradation of specific RNAs expressed in undifferentiated germ cells. These regulators target RNAs enriched for cytidine sequences that are bound by the polypyrimidine tract binding protein Half pint. Thus, RNA degradation helps orchestrate a germ cell-to-maternal transition that gives rise to the maternal contribution to the zygote.
在有性生殖的动物中,卵母细胞提供了大量的 RNA,这些 RNA 对于受精后胚胎的发育是必不可少的。然而,调控卵母细胞发生过程中母体 RNA 组成的机制尚不清楚。本文中,作者发现卵母细胞特化过程中,一部分在卵母细胞发生早期表达的 RNA 会受到调控降解。如果这些 RNA 不能被有效去除,将会导致卵母细胞功能障碍和死亡。作者鉴定到 Super Killer 复合物和 No-Go Decay 因子 Pelota 是调控卵母细胞发生的关键因子,通过靶向降解未分化生殖细胞中特异性表达的 RNA 发挥作用。这些调控因子靶向富含胞嘧啶序列的 RNA,这些 RNA 与多嘧啶序列结合蛋白 Half pint 结合。因此,RNA 降解有助于协调从生殖细胞到母体的转变,从而为合子提供母体贡献。