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A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326793/ https://www.ncbi.nlm.nih.gov/pubmed/30335155 http://dx.doi.org/10.1093/nar/gky971 |
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author | Dai, Xing-Xing Jiang, Jun-Chao Sha, Qian-Qian Jiang, Yu Ou, Xiang-Hong Fan, Heng-Yu |
author_facet | Dai, Xing-Xing Jiang, Jun-Chao Sha, Qian-Qian Jiang, Yu Ou, Xiang-Hong Fan, Heng-Yu |
author_sort | Dai, Xing-Xing |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6326793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63267932019-01-15 A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte Dai, Xing-Xing Jiang, Jun-Chao Sha, Qian-Qian Jiang, Yu Ou, Xiang-Hong Fan, Heng-Yu Nucleic Acids Res RNA and RNA-protein complexes 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. Oxford University Press 2019-01-10 2018-10-18 /pmc/articles/PMC6326793/ /pubmed/30335155 http://dx.doi.org/10.1093/nar/gky971 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA and RNA-protein complexes Dai, Xing-Xing Jiang, Jun-Chao Sha, Qian-Qian Jiang, Yu Ou, Xiang-Hong Fan, Heng-Yu A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte |
title | A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte |
title_full | A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte |
title_fullStr | A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte |
title_full_unstemmed | A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte |
title_short | A combinatorial code for mRNA 3′-UTR-mediated translational control in the mouse oocyte |
title_sort | combinatorial code for mrna 3′-utr-mediated translational control in the mouse oocyte |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326793/ https://www.ncbi.nlm.nih.gov/pubmed/30335155 http://dx.doi.org/10.1093/nar/gky971 |
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