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Homozygous Loss of , but not its Haploinsufficiency, Leads to Male Infertility and Fertilization Failure. | LitMetric

Homozygous Loss of , but not its Haploinsufficiency, Leads to Male Infertility and Fertilization Failure.

Front Cell Dev Biol

Tianjin Union Medical Center, State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Protein Sciences, Frontiers Science Center for Cell Responses, National Demonstration Center for Experimental Biology Education and College of Life Sciences, Nankai University, Institute of Translational Medicine, Tianjin, China.

Published: April 2022

The gene has been associated with male infertility. Male chimera mice were infertile, supporting the prevailing view that haploinsufficiency causes male infertility. In this study, we identified a heterozygous mutation on , c.72C>A (p.Cys24Ter) in the male partner of a patient couple, who had a previous fertilization failure (FF) after intracytoplasmic sperm injection (ICSI) and became pregnant after ICSI together with artificial oocyte activation (AOA). To investigate the role of in FF and oocyte activation, we constructed knockout mice. Surprisingly, male mice, but not male mice, are infertile, and have reduced sperm counts and abnormal sperm morphology. Importantly, AOA treatment enhances the 2-cell embryo rate of ICSI embryos injected with sperm, indicating that FF caused by male deficiency is overcome by AOA. Mechanistically, loss of PLCζ around the acrosome might be the reason for FF of sperm. Taken together, our data indicated that homozygous knockout of , but not haploinsufficiency, leads to male infertility and FF.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082362PMC
http://dx.doi.org/10.3389/fcell.2022.850052DOI Listing

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