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LSM14B Controls Oocyte MRNA Storage and Stability to Ensure Female Fertility

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Publisher Springer
Specialty Biology
Date 2023 Aug 14
PMID 37578641
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Abstract

Controlled mRNA storage and stability is essential for oocyte meiosis and early embryonic development. However, how to regulate mRNA storage and stability in mammalian oogenesis remains elusive. Here we showed that LSM14B, a component of membraneless compartments including P-body-like granules and mitochondria-associated ribonucleoprotein domain (MARDO) in germ cell, is indispensable for female fertility. To reveal loss of LSM14B disrupted primordial follicle assembly and caused mRNA reduction in non-growing oocytes, which was concomitant with the impaired assembly of P-body-like granules. 10× Genomics single-cell RNA-sequencing and immunostaining were performed. Meanwhile, we conducted RNA-seq analysis of GV-stage oocytes and found that Lsm14b deficiency not only impaired the maternal mRNA accumulation but also disrupted the translation in fully grown oocytes, which was closely associated with dissolution of MARDO components. Moreover, Lsm14b-deficient oocytes reassembled a pronucleus containing decondensed chromatin after extrusion of the first polar body, through compromising the activation of maturation promoting factor, while the defects were restored via WEE1/2 inhibitor. Together, our findings reveal that Lsm14b plays a pivotal role in mammalian oogenesis by specifically controlling of oocyte mRNA storage and stability.

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References
1.
Wang J, Ge W, Zhai Q, Liu J, Sun X, Liu W . Single-cell transcriptome landscape of ovarian cells during primordial follicle assembly in mice. PLoS Biol. 2020; 18(12):e3001025. PMC: 7787681. DOI: 10.1371/journal.pbio.3001025. View

2.
He Y, Chen Q, Dai J, Cui Y, Zhang C, Wen X . Single-cell RNA-Seq reveals a highly coordinated transcriptional program in mouse germ cells during primordial follicle formation. Aging Cell. 2021; 20(7):e13424. PMC: 8282241. DOI: 10.1111/acel.13424. View

3.
Tingen C, Kim A, Woodruff T . The primordial pool of follicles and nest breakdown in mammalian ovaries. Mol Hum Reprod. 2009; 15(12):795-803. PMC: 2776475. DOI: 10.1093/molehr/gap073. View

4.
Gu C, Liu S, Wu Q, Zhang L, Guo F . Integrative single-cell analysis of transcriptome, DNA methylome and chromatin accessibility in mouse oocytes. Cell Res. 2018; 29(2):110-123. PMC: 6355938. DOI: 10.1038/s41422-018-0125-4. View

5.
Gosden R . Oogenesis as a foundation for embryogenesis. Mol Cell Endocrinol. 2002; 186(2):149-53. DOI: 10.1016/s0303-7207(01)00683-9. View