A TESTICULAR PROTEIN IMPORTANT FOR FERTILITY HAS GLUTATHIONE-S-TRANSFERASE ACTIVITY AND IS LOCALIZED EXTRACELLULARLY IN THE SEMINIFEROUS TUBULES

A 24-kDa protein isolated by preparative gel electrophoresis from rat testes was reported by us as an active immunogen in rats. Anti-24-kDa antibodies inhibited murine sperm-oocyte binding in vitro. Here, we sh ow similarity at the NH2 terminus shared by this protein purified on S ephadex G-75 followed by anion exchange high performance liquid chroma tography with glutathione S-transferase (GST)-mu subunits. This protei n purified by glutathione affinity chromatography also demonstrated si milarity to GST-mu NH2 terminus in a 30-amino-acid overlap. Both prote ins showed activity toward the GST substrate 1-chloro-2,4-dinitrobenze ne (K-m of 33 mu M and 50 mu M) which was inhibited by 17 beta-estradi ol 3-sulfate. Antisera against both proteins recognized liver GST-mu o n Western blots and sperm acrosome of multiple species immunocytochemi cally. Both antisera significantly inhibited in vitro fertilization of goat oocytes by sperm preincubated with them while anti-liver GST ser a did not. GST activity was localized on rat sperm, seminiferous tubul ar fluid, and Sertoli cells. Seminiferous tubular fluid 24-kDa protein shared similarity to the NH2 terminus of GST-mu subunits in a 20-amin o-acid overlap. Time dependent accumulation of GST was detected in the spent culture medium of seminiferous tubules from rats of different a ges suggesting secretion.