Animal reproduction science · 2026
Expression,co-localization and interaction analysis of mitochondrial membrane proteins prohibitin and stomatin-like protein 2 during spermatogenesis in Larimichthys polyactis.
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Wang Li, Dai Wenying, Liu Yang, Chu Shifan, Chen Yiner, Hou Congcong, Liu Feng, Zhu Junquan, Lou Bao
Аннотация
To investigate the potential functions of mitochondrial membrane proteins prohibitin (PHB) and stomatin-like protein 2 (SLP2) during spermatogenesis in Larimichthys polyactis, we analyze the molecular characteristics and expression profiles of Lp-PHB and Lp-SLP2, the co-localization characteristics of Lp-PHB, Lp-SLP2 and mitochondria during spermatogenesis, as well as the co-localization characteristics of Lp-PHB, ubiquitin, and mitochondria. The results showed that Lp-PHB consists of an N-terminal hydrophobic, a conserved SPFH domain and a C-terminal helical domain, while Lp-SLP2 only contains a conserved SPFH domain. Lp-PHB and Lp-SLP2 genes and their encoded proteins were highly expressed in the testis, Lp-PHB and Lp-SLP2 protein were localized in the mitochondria of spermatogenic cells. During spermatogenesis, the signals of Lp-PHB and Lp-SLP2, Lp-PHB and mitochondria, as well as Lp-SLP2 and mitochondria were co-localized: in spermatogonia and spermatocytes, the co-localization signals were randomly distributed in the perinuclear cytoplasm; during the differentiation of spermatids into sperm, the co-localization signals gradually migrated to the tail region on one side of the nucleus; and in mature sperm, the co-localization signals accumulated in the middle piece. Additionally, the signals of Lp-PHB and ubiquitin, as well as ubiquitin and mitochondria, were also consistently co-localized during spermatogenesis, with co-localization characteristics highly similar to those of Lp-PHB and mitochondria. These results suggest that Lp-PHB and Lp-SLP2 may cooperate through interaction to maintain mitochondrial functional homeostasis during spermatogenesis in L. polyactis, and Lp-PHB may be involved in the degradation of damaged or excess mitochondria by mediating mitochondrial ubiquitination, thereby facilitating the normal progression of spermatogenesis.