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High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development

High-resolution ribosome fractionation and low-input ribosome profiling of bovine oocytes and preimplantation embryos has enabled us to define the translational landscapes of early embryo development at an unprecedented level. We analyzed the transcriptome and the polysome- and non-polysome-bound RN...

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Autores principales: Zhu, Linkai, Zhou, Tong, Iyyappan, Rajan, Ming, Hao, Dvoran, Michal, Wang, Yinjuan, Chen, Qi, Roberts, R. Michael, Susor, Andrej, Jiang, Zongliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687001/
https://www.ncbi.nlm.nih.gov/pubmed/36227586
http://dx.doi.org/10.1242/dev.200819
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author Zhu, Linkai
Zhou, Tong
Iyyappan, Rajan
Ming, Hao
Dvoran, Michal
Wang, Yinjuan
Chen, Qi
Roberts, R. Michael
Susor, Andrej
Jiang, Zongliang
author_facet Zhu, Linkai
Zhou, Tong
Iyyappan, Rajan
Ming, Hao
Dvoran, Michal
Wang, Yinjuan
Chen, Qi
Roberts, R. Michael
Susor, Andrej
Jiang, Zongliang
author_sort Zhu, Linkai
collection PubMed
description High-resolution ribosome fractionation and low-input ribosome profiling of bovine oocytes and preimplantation embryos has enabled us to define the translational landscapes of early embryo development at an unprecedented level. We analyzed the transcriptome and the polysome- and non-polysome-bound RNA profiles of bovine oocytes (germinal vesicle and metaphase II stages) and early embryos at the two-cell, eight-cell, morula and blastocyst stages, and revealed four modes of translational selectivity: (1) selective translation of non-abundant mRNAs; (2) active, but modest translation of a selection of highly expressed mRNAs; (3) translationally suppressed abundant to moderately abundant mRNAs; and (4) mRNAs associated specifically with monosomes. A strong translational selection of low-abundance transcripts involved in metabolic pathways and lysosomes was found throughout bovine embryonic development. Notably, genes involved in mitochondrial function were prioritized for translation. We found that translation largely reflected transcription in oocytes and two-cell embryos, but observed a marked shift in the translational control in eight-cell embryos that was associated with the main phase of embryonic genome activation. Subsequently, transcription and translation become more synchronized in morulae and blastocysts. Taken together, these data reveal a unique spatiotemporal translational regulation that accompanies bovine preimplantation development.
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spelling pubmed-96870012022-12-16 High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development Zhu, Linkai Zhou, Tong Iyyappan, Rajan Ming, Hao Dvoran, Michal Wang, Yinjuan Chen, Qi Roberts, R. Michael Susor, Andrej Jiang, Zongliang Development Research Article High-resolution ribosome fractionation and low-input ribosome profiling of bovine oocytes and preimplantation embryos has enabled us to define the translational landscapes of early embryo development at an unprecedented level. We analyzed the transcriptome and the polysome- and non-polysome-bound RNA profiles of bovine oocytes (germinal vesicle and metaphase II stages) and early embryos at the two-cell, eight-cell, morula and blastocyst stages, and revealed four modes of translational selectivity: (1) selective translation of non-abundant mRNAs; (2) active, but modest translation of a selection of highly expressed mRNAs; (3) translationally suppressed abundant to moderately abundant mRNAs; and (4) mRNAs associated specifically with monosomes. A strong translational selection of low-abundance transcripts involved in metabolic pathways and lysosomes was found throughout bovine embryonic development. Notably, genes involved in mitochondrial function were prioritized for translation. We found that translation largely reflected transcription in oocytes and two-cell embryos, but observed a marked shift in the translational control in eight-cell embryos that was associated with the main phase of embryonic genome activation. Subsequently, transcription and translation become more synchronized in morulae and blastocysts. Taken together, these data reveal a unique spatiotemporal translational regulation that accompanies bovine preimplantation development. The Company of Biologists Ltd 2022-11-03 /pmc/articles/PMC9687001/ /pubmed/36227586 http://dx.doi.org/10.1242/dev.200819 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Zhu, Linkai
Zhou, Tong
Iyyappan, Rajan
Ming, Hao
Dvoran, Michal
Wang, Yinjuan
Chen, Qi
Roberts, R. Michael
Susor, Andrej
Jiang, Zongliang
High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
title High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
title_full High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
title_fullStr High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
title_full_unstemmed High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
title_short High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
title_sort high-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687001/
https://www.ncbi.nlm.nih.gov/pubmed/36227586
http://dx.doi.org/10.1242/dev.200819
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