PSMA8‐Containing 20S Proteasome Regulates Spermiogenesis and Male Fertility
Year: 2026
Type: article
Abstract: ABSTRACT Proteasome experiences sophisticated dynamics in types, quantities, and activities during spermiogenesis. However, the physiological importance of proteasomal degradation in mammalian spermiogenesis remains largely unknown. Here, we report that the PSMA8‐containing spermato‐20S proteasome (s20S) is required for spermiogenesis and male fertility in mice. In a mutant mouse model that the C‐terminal 30‐amino‐acid (C30) of PSMA8 is substituted by PSMA7‐C30, the resulting PSMA8 7C30 protein is unstable, which further disrupts the assembly of s20S and subcellular localization of 19S regulatory particle in testes. Psma8 7C30 males could produce round spermatids, but sperm formation is delayed and abnormal, exhibiting a phenotype of oligoasthenoteratozoospermia. s20S is required for the ubiquitination‐dependent proteasomal degradation of a group of proteins in elongating spermatids. These s20S‐mediated degradation events are essential for liquid‐liquid phase separation of FXR1 and thereby translational‐activation of its substrates. Taken together, these findings provide an in vivo evidence of protein homeostasis control in spermiogenesis in mammals.
Source: Advanced Science
Authors: Huiwen Cao, Qianting Zhang, Wei Xu, Anxuan Fang, Haomang Xu, Cheng Qiu, Lugeng He, Chao Yu
Language: English
Subfield: Reproductive Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $6,730
OpenAlex ID: W7154157365
