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

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    0569567 - ÚŽFG 2023 RIV GB eng J - Journal Article
    Zhu, L. - Zhou, T. - Iyyappan, Rajan - Ming, H. - Dvořan, Michal - Wang, Y. - Chen, Q. - Roberts, R. M. - Šušor, Andrej - Jiang, Z.
    High-resolution ribosome profiling reveals translational selectivity for transcripts in bovine preimplantation embryo development.
    Development. Roč. 149, č. 21 (2022), č. článku dev200819. ISSN 0950-1991. E-ISSN 1477-9129
    R&D Projects: GA ČR(CZ) GA22-27301S
    Institutional support: RVO:67985904
    Keywords : ribosome profiling * translational selectivity * translation
    OECD category: Developmental biology
    Impact factor: 4.6, year: 2022
    Method of publishing: Open access
    https://journals.biologists.com/dev/article/149/21/dev200819/280468/High-resolution-ribosome-profiling-reveals

    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.
    Permanent Link: https://hdl.handle.net/11104/0340965

     
     
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