LSM14B is an Oocyte‐Specific RNA‐Binding Protein Indispensable for Maternal mRNA Metabolism and Oocyte Development in Mice

Author:

Li Hui12ORCID,Zhao Hailian3ORCID,Yang Chunhui1ORCID,Su Ruibao3ORCID,Long Min12ORCID,Liu Jinliang1ORCID,Shi Lanying12,Xue Yuanchao3ORCID,Su You‐Qiang124ORCID

Affiliation:

1. Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology School of Life Sciences Shandong University Qingdao 266237 P. R. China

2. State Key Laboratory of Reproductive Medicine Nanjing Medical University Nanjing 211126 P. R. China

3. Institute of Biophysics Chinese Academy of Sciences Beijing 100101 P. R. China

4. Collaborative Innovation Center of Genetics and Development Fudan University Shanghai 200433 P. R. China

Abstract

AbstractMammalian oogenesis features reliance on the mRNAs produced and stored during early growth phase. These are essential for producing an oocyte competent to undergo meiotic maturation and embryogenesis later when oocytes are transcriptionally silent. The fate of maternal mRNAs hence ensures the success of oogenesis and the quality of the resulting eggs. Nevertheless, how the fate of maternal mRNAs is determined remains largely elusive. RNA‐binding proteins (RBPs) are crucial regulators of oogenesis, yet the identity of the full complement of RBPs expressed in oocytes is unknown. Here, a global view of oocyte‐expressed RBPs is presented: mRNA‐interactome capture identifies 1396 RBPs in mouse oocytes. An analysis of one of these RBPs, LSM family member 14 (LSM14B), demonstrates that this RBP is specific to oocytes and associated with many networks essential for oogenesis. Deletion of Lsm14b results in female‐specific infertility and a phenotype characterized by oocytes incompetent to complete meiosis and early embryogenesis. LSM14B serves as an interaction hub for proteins and mRNAs throughout oocyte development and regulates translation of a subset of its bound mRNAs. Therefore, RNP complexes tethered by LSM14B are found exclusively in oocytes and are essential for the control of maternal mRNA fate and oocyte development.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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