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SERBP1 Promotes Stress Granule Clearance by Regulating 26S Proteasome Activity and G3BP1 Ubiquitination and Protects Male Germ Cells from Thermostimuli Damage

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摘要 Stress granules(SGs)are membraneless cytoplasmic condensates that dynamically assemble in response to various stressors and reversibly disassemble after stimulus removal;however,the mechanisms underlying SG dynamics and their physiological roles in germ cell development are elusive.Here,we show that SERBP1(SERPINE1 mRNA binding protein 1)is a universal SG component and conserved regulator of SG clearance in somatic and male germ cells.SERBP1 interacts with the SG core component G3BP1 and 26S proteasome proteins PSMD10 and PSMA3 and recruits them to SGs.In the absence of SERBP1,reduced 20S proteasome activity,mislocalized valosin containing protein(VCP)and Fas associated factor family member 2(FAF2),and diminished K63-linked polyubiquitination of G3BP1 during the SG recovery period were observed.Interestingly,the depletion of SERBP1 in testicular cells in vivo causes increased germ cell apoptosis upon scrotal heat stress.Accordingly,we propose that a SERBP1-mediated mechanism regulates 26S proteasome activity and G3BP1 ubiquitination to facilitate SG clearance in both somatic and germ cell lines.
出处 《Research》 SCIE EI CSCD 2023年第4期671-688,共18页 研究(英文)
基金 This work,in part,was supported by grants from the National Natural Science Foundation of China(82171605 to S.Y.and 31900511 to F.W.) the Fundamental Research Funds for the Central Universities,Huazhong University of Science and Technology(No.2019kfyXJJS089 to F.W.)。
关键词 G3BP1 depletion ABSENCE
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