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CEP128 is involved in spermatogenesis in humans and mice.

Nature communications (2022-03-18)
Xueguang Zhang, Lingbo Wang, Yongyi Ma, Yan Wang, Hongqian Liu, Mohan Liu, Lang Qin, Jinghong Li, Chuan Jiang, Xiaojian Zhang, Xudong Shan, Yuliang Liu, Jinsong Li, Yaqian Li, Rui Zheng, Yongkang Sun, Jianfeng Sun, Xiangyou Leng, Yan Liang, Feng Zhang, Xiaohui Jiang, Yihong Yang, Ying Shen
ABSTRACT

Centrosomal proteins are necessary components of the centrosome, a conserved eukaryotic organelle essential to the reproductive process. However, few centrosomal proteins have been genetically linked to fertility. Herein we identify a homozygous missense variant of CEP128 (c.665 G > A [p.R222Q]) in two infertile males. Remarkably, male homozygous knock-in mice harboring the orthologous CEP128R222Q variant show anomalies in sperm morphology, count, and motility. Moreover, Cep128 knock-out mice manifest male infertility associated with disrupted sperm quality. We observe defective sperm flagella in both homozygous Cep128 KO and KI mice; the cilia development in other organs is normal-suggesting that CEP128 variants predominantly affected the ciliogenesis in the testes. Mechanistically, CEP128 is involved in male reproduction via regulating the expression of genes and/or the phosphorylation of TGF-β/BMP-signalling members during spermatogenesis. Altogether, our findings unveil a crucial role for CEP128 in male fertility and provide important insights into the functions of centrosomal proteins in reproductive biology.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Anti-CEP128 antibody produced in rabbit, Ab1, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
Sigma-Aldrich
Phosphatase Inhibitor Cocktail 2, aqueous solution (dark coloration may develop upon storage, which does not affect the activity)