Maternal mRNAs with distinct 3′ UTRs define the temporal pattern of Ccnb1 synthesis during mouse oocyte meiotic maturation

被引:50
作者
Yang, Ye [1 ,2 ,3 ,4 ]
Yang, Cai-Rong [2 ,3 ,4 ]
Han, Seung Jin [2 ,3 ,4 ,5 ]
Daldello, Enrico Maria [2 ,3 ,4 ]
Cho, Ara [2 ,3 ,4 ]
Martins, Joao P. Sousa [2 ,3 ,4 ]
Xia, Guoliang [1 ]
Conti, Marco [2 ,3 ,4 ]
机构
[1] China Agr Univ, Coll Biol Sci, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China
[2] Univ Calif San Francisco, Ctr Reprod Sci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Obstet & Gynecol & Reprod Sci, San Francisco, CA 94143 USA
[5] Inje Univ, Dept Biol Sci, Gimhae 621749, South Korea
基金
美国国家卫生研究院;
关键词
APA; cyclins; meiosis; oocyte; translation; CYTOPLASMIC POLYADENYLATION; ALTERNATIVE POLYADENYLATION; CYCLIC-GMP; TRANSLATION; EXPRESSION; ARREST; DAZL;
D O I
10.1101/gad.296871.117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The final stages of female gamete maturation occur in the virtual absence of transcription, with gene expression driven by a program of selective unmasking, translation, and degradation of maternal mRNAs. Here we demonstrate that the timing of Ccnb1 mRNA translation in mouse oocytes is dependent on the presence of transcripts with different 3' untranslated regions (UTRs). This 3' UTR heterogeneity directs distinct temporal patterns of translational activation or repression. Inclusion or exclusion of cis-acting elements is responsible for these divergent regulations. Our findings reveal an additional layer of translation control through alternative polyadenylation usage required to fine-tune the timing of meiosis progression.
引用
收藏
页码:1302 / 1307
页数:6
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