N6-Methyladenosine Sequencing Highlights the Involvement of mRNA Methylation in Oocyte Meiotic Maturation and Embryo Development by Regulating Translation in Xenopus laevis

被引:69
作者
Qi, Shu-Tao [1 ]
Ma, Jun-Yu [2 ]
Wang, Zhen-Bo [1 ]
Guo, Lei [1 ]
Hou, Yi [1 ]
Sun, Qing-Yuan [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, Beijing 100101, Peoples R China
[2] Qingdao Agr Univ, Coll Anim Sci & Technol, Qingdao 266109, Peoples R China
关键词
CYTOPLASMIC POLYADENYLATION; GENOME ACTIVATION; DNA-REPLICATION; ZYGOTIC GENOME; NUCLEAR-RNA; PROTEIN; MOS; CPEB; N6-METHYLADENOSINE; PHOSPHORYLATION;
D O I
10.1074/jbc.M116.748889
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-6-methyladenosine (m(6)A) modified mRNAs in fully grown germinal vesicle-stage and metaphase II-stage oocytes. As a result, we identified 4207 mRNAs with m(6)A 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.
引用
收藏
页码:23020 / 23026
页数:7
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