» Articles » PMID: 34031364

The Essential Roles of Mps1 in Spermatogenesis and Fertility in Mice

Overview
Journal Cell Death Dis
Date 2021 May 25
PMID 34031364
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Monopolar spindle 1 (MPS1), which plays a critical role in somatic mitosis, has also been revealed to be essential for meiosis I in oocytes. Spermatogenesis is an important process involving successive mitosis and meiosis, but the function of MPS1 in spermatogenesis remains unclear. Here, we generated Mps1 conditional knockout mice and found that Ddx4-cre-driven loss of Mps1 in male mice resulted in depletion of undifferentiated spermatogonial cells and subsequently of differentiated spermatogonia and spermatocytes. In addition, Stra8-cre-driven ablation of Mps1 in male mice led to germ cell loss and fertility reduction. Spermatocytes lacking Mps1 have blocked at the zygotene-to-pachytene transition in the prophase of meiosis I, which may be due to decreased H2B ubiquitination level mediated by MDM2. And the expression of many meiotic genes was decreased, while that of apoptotic genes was increased. Moreover, we also detected increased apoptosis in spermatocytes with Mps1 knockout, which may have been the reason why germ cells were lost. Taken together, our findings indicate that MPS1 is required for mitosis of gonocytes and spermatogonia, differentiation of undifferentiated spermatogonia, and progression of meiosis I in spermatocytes.

Citing Articles

Male germ cells with Bag5 deficiency show reduced spermiogenesis and exchange of basic nuclear proteins.

Cao Y, Wang S, Qin Z, Xiong Q, Liu J, Li W Cell Mol Life Sci. 2025; 82(1):92.

PMID: 39992433 PMC: 11850669. DOI: 10.1007/s00018-025-05591-2.


Role of spindle assembly checkpoint proteins in gametogenesis and embryogenesis.

Pun R, North B Front Cell Dev Biol. 2025; 12:1491394.

PMID: 39911185 PMC: 11794522. DOI: 10.3389/fcell.2024.1491394.


Annexin A2 combined with TTK accelerates esophageal cancer progression via the Akt/mTOR signaling pathway.

Liu R, Lu Y, Li J, Yao W, Wu J, Chen X Cell Death Dis. 2024; 15(4):291.

PMID: 38658569 PMC: 11043348. DOI: 10.1038/s41419-024-06683-w.


BMAL1-TTK-H2Bub1 loop deficiency contributes to impaired BM-MSC-mediated bone formation in senile osteoporosis.

Jinteng L, Peitao X, Wenhui Y, Guiwen Y, Feng Y, Xiaojun X Mol Ther Nucleic Acids. 2023; 31:568-585.

PMID: 36910712 PMC: 9996134. DOI: 10.1016/j.omtn.2023.02.014.


G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice.

Yun D, Zhou L, Shi J, Li X, Wu X, Sun F PeerJ. 2022; 10:e13532.

PMID: 35782098 PMC: 9248785. DOI: 10.7717/peerj.13532.

References
1.
Fuchs Y, Steller H . Programmed cell death in animal development and disease. Cell. 2011; 147(4):742-58. PMC: 4511103. DOI: 10.1016/j.cell.2011.10.033. View

2.
Li M, Sun S, Priest J, Bi X, Fan Y . Characterization of TNF-induced cell death in Drosophila reveals caspase- and JNK-dependent necrosis and its role in tumor suppression. Cell Death Dis. 2019; 10(8):613. PMC: 6692325. DOI: 10.1038/s41419-019-1862-0. View

3.
Keeney S, Giroux C, Kleckner N . Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family. Cell. 1997; 88(3):375-84. DOI: 10.1016/s0092-8674(00)81876-0. View

4.
La H, Hobbs R . Mechanisms regulating mammalian spermatogenesis and fertility recovery following germ cell depletion. Cell Mol Life Sci. 2019; 76(20):4071-4102. PMC: 11105665. DOI: 10.1007/s00018-019-03201-6. View

5.
Li X, Long X, Xie Y, Zeng X, Chen X, Mo Z . The roles of retinoic acid in the differentiation of spermatogonia and spermatogenic disorders. Clin Chim Acta. 2019; 497:54-60. DOI: 10.1016/j.cca.2019.07.013. View