Phosphoproteome analysis of the crosstalk between sumoylation and phosphorylation in mouse spermatocytes.

Spermatogenesis is supported by various posttranslational modifications. There is growing evidence supporting a crosstalk between sumoylation and phosphorylation in different cell types. We have recently shown that inhibition of global sumoylation with a sumoylation inhibitor (Ginkgolic acid, GA) arrested purified mouse spermatocytes in vitro ; the spermatocytes could not condense chromatin and disassemble the synaptonemal complex. Our data have also revealed that some kinases regulating the meiotic prophase (PLK1 and AURKB) were inhibited upon the inhibition of sumoylation. Nevertheless, specific phosphorylated targets affected by the inhibition of sumoylation have not been identified. To address this gap, in this study, we performed a comparative phospho-proteome analysis of the control spermatocytes and spermatocytes treated with the GA. Our analysis has narrowed down to several proteins implicated in the regulation of cell cycle and/or meiosis. Two of these targets, NPM1 and hnRNPH1, were studied further using western blotting in both cell lines and primary cells. Decrease in sumoylaion-dependend phosphorylation of NPM1 on Ser125 regulated by AURKB can be a contributing factor to the inability of spermatocytes to condense chromatin by the end of the prophase and should be studied further. • Downregulation of sumoylation causes changes in phosphorylation of important spermatocyte proteins. • Sumoylation regulates NPM1 in GC-1 spermatogonia and mouse spermatocytes. • Sumoylation regulates hnRNPH1 in GC-1 spermatogonia mouse spermatocytes. • Phosphorylation of NPM1 on Ser125 regulated by AURKB should be studied further. [ABSTRACT FROM AUTHOR]