Qi Shu-Tao, Ma Jun-Yu, Wang Zhen-Bo, Guo Lei, Hou Yi, Sun Qing-Yuan
From the State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China and.
the College of Animal Science and Technology, Qingdao Agricultural University, Qingdao 266109, China.
J Biol Chem. 2016 Oct 28;291(44):23020-23026. doi: 10.1074/jbc.M116.748889. Epub 2016 Sep 9.
During the oogenesis of Xenopus laevis, oocytes accumulate maternal materials for early embryo development. As the transcription activity of the oocyte is silenced at the fully grown stage and the global genome is reactivated only by the mid-blastula embryo stage, the translation of maternal mRNAs accumulated during oocyte growth should be accurately regulated. Previous evidence has illustrated that the poly(A) tail length and RNA binding elements mediate RNA translation regulation in the oocyte. Recently, RNA methylation has been found to exist in various systems. In this study, we sequenced the N-methyladenosine (mA) modified mRNAs in fully grown germinal vesicle-stage and metaphase II-stage oocytes. As a result, we identified 4207 mRNAs with mA peaks in germinal vesicle-stage or metaphase II-stage oocytes. When we integrated the mRNA methylation data with transcriptome and proteome data, we found that the highly methylated mRNAs showed significantly lower protein levels than those of the hypomethylated mRNAs, although the RNA levels showed no significant difference. We also found that the hypomethylated mRNAs were mainly enriched in the cell cycle and translation pathways, whereas the highly methylated mRNAs were mainly associated with protein phosphorylation. Our results suggest that oocyte mRNA methylation can regulate cellular translation and cell division during oocyte meiotic maturation and early embryo development.
在非洲爪蟾的卵子发生过程中,卵母细胞积累母体物质用于早期胚胎发育。由于卵母细胞的转录活性在完全成熟阶段被沉默,并且只有到囊胚中期胚胎阶段全基因组才会重新激活,因此在卵母细胞生长过程中积累的母体mRNA的翻译应该得到精确调控。先前的证据表明,多聚腺苷酸(poly(A))尾长度和RNA结合元件介导卵母细胞中的RNA翻译调控。最近,人们发现RNA甲基化存在于各种系统中。在本研究中,我们对完全成熟的生发泡期和中期II期卵母细胞中N-甲基腺苷(m⁶A)修饰的mRNA进行了测序。结果,我们在生发泡期或中期II期卵母细胞中鉴定出4207个具有m⁶A峰的mRNA。当我们将mRNA甲基化数据与转录组和蛋白质组数据整合时,我们发现,尽管RNA水平没有显著差异,但高度甲基化的mRNA的蛋白质水平明显低于低甲基化的mRNA。我们还发现,低甲基化的mRNA主要富集在细胞周期和翻译途径中,而高度甲基化的mRNA主要与蛋白质磷酸化相关。我们的结果表明,卵母细胞mRNA甲基化可以在卵母细胞减数分裂成熟和早期胚胎发育过程中调节细胞翻译和细胞分裂。