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mRNA 3'-UTR 介导的翻译调控在小鼠卵母细胞中的组合编码。

A combinatorial code for mRNA 3'-UTR-mediated translational control in the mouse oocyte.

机构信息

MOEKey Laboratory for Biosystems Homeostasis & Protection and InnovationCenter for Cell Signaling Network, Life Sciences Institute, Zhejiang University, Hangzhou 310058, China.

Fertility Preservation Laboratory, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.

出版信息

Nucleic Acids Res. 2019 Jan 10;47(1):328-340. doi: 10.1093/nar/gky971.

DOI:10.1093/nar/gky971
PMID:30335155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6326793/
Abstract

Meiotic maturation of mammalian oocytes depends on the temporally and spatially regulated cytoplasmic polyadenylation and translational activation of maternal mRNAs. Cytoplasmic polyadenylation is controlled by cis-elements in the 3'-UTRs of mRNAs including the polyadenylation signal (PAS), which is bound by the cleavage and polyadenylation specificity factor (CPSF) and the cytoplasmic polyadenylation element (CPE), which recruits CPE binding proteins. Using the 3'-UTRs of mouse Cpeb1, Btg4 and Cnot6l mRNAs, we deciphered the combinatorial code that controls developmental stage-specific translation during meiotic maturation: (i) translation of a maternal transcript at the germinal vesicle (GV) stage requires one or more PASs that locate far away from CPEs; (ii) PASs distal and proximal to the 3'-end of the transcripts are equally effective in mediating translation at the GV stage, as long as they are not close to the CPEs; (iii) Both translational repression at the GV stage and activation after germinal vesicle breakdown require at least one CPE adjacent to the PAS; (iv) The numbers and positions of CPEs in relation to PASs within the 3'-UTR of a given transcript determines its repression efficiency in GV oocytes. This study reveals a previously unrecognized non-canonical mechanism by which the proximal PASs mediate 3'-terminal polyadenylation and translation of maternal transcripts.

摘要

哺乳动物卵母细胞的减数分裂成熟依赖于母体 mRNA 的时空调节的细胞质多聚腺苷酸化和翻译激活。细胞质多聚腺苷酸化由 mRNA 的 3'UTR 中的顺式元件控制,包括多聚腺苷酸化信号 (PAS),它被切割和多聚腺苷酸化特异性因子 (CPSF) 结合,细胞质多聚腺苷酸化元件 (CPE) 招募 CPE 结合蛋白。使用小鼠 Cpeb1、Btg4 和 Cnot6l mRNA 的 3'UTR,我们破解了控制减数分裂成熟过程中发育阶段特异性翻译的组合密码:(i) 在生发泡 (GV) 阶段翻译母体转录本需要一个或多个远离 CPE 的 PAS;(ii) 转录本 3'末端的远侧和近侧 PAS 在 GV 阶段同样有效地介导翻译,只要它们不靠近 CPE;(iii) 在 GV 阶段的翻译抑制和细胞质破裂后的激活都需要至少一个邻近 PAS 的 CPE;(iv) 在给定转录本的 3'UTR 中 PAS 相对于 CPE 的数量和位置决定了其在 GV 卵母细胞中的抑制效率。这项研究揭示了一种以前未被认识的非典型机制,即近端 PAS 介导母体转录本的 3'末端多聚腺苷酸化和翻译。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/6136a13b326c/gky971fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/ee4b3a4c296a/gky971fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/18b0f037d101/gky971fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/aac5b1e7c6ff/gky971fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/031bf9ccac73/gky971fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/f83a73ed69cc/gky971fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/e81f54ef501f/gky971fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/6136a13b326c/gky971fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/ee4b3a4c296a/gky971fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/18b0f037d101/gky971fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/aac5b1e7c6ff/gky971fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/031bf9ccac73/gky971fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/f83a73ed69cc/gky971fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/e81f54ef501f/gky971fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc5/6326793/6136a13b326c/gky971fig7.jpg

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