@article {11895, title = {Heat shock protein 90 functions to stabilize and activate the testis-specific serine/threonine kinases, a family of kinases essential for male fertility.}, journal = {J Biol Chem}, volume = {288}, year = {2013}, month = {2013 Jun 7}, pages = {16308-20}, abstract = {

Spermiogenesis is characterized by a profound morphological differentiation of the haploid spermatid into spermatozoa. The testis-specific serine/threonine kinases (TSSKs) comprise a family of post-meiotic kinases expressed in spermatids, are critical to spermiogenesis, and are required for male fertility in mammals. To explore the role of heat shock protein 90 (HSP90) in regulation of TSSKs, the stability and catalytic activity of epitope-tagged murine TSSKs were assessed in 293T and COS-7 cells. TSSK1, -2, -4, and -6 (small serine/threonine kinase) were all found to associate with HSP90, and pharmacological inhibition of HSP90 function using the highly specific drugs 17-AAG, SNX-5422, or NVP-AUY922 reduced TSSK protein levels in cells. The attenuation of HSP90 function abolished the catalytic activities of TSSK4 and -6 but did not significantly alter the specific activities of TSSK1 and -2. Inhibition of HSP90 resulted in increased TSSK ubiquitination and proteasomal degradation, indicating that HSP90 acts to control ubiquitin-mediated catabolism of the TSSKs. To study HSP90 and TSSKs in germ cells, a mouse primary spermatid culture model was developed and characterized. Using specific antibodies against murine TSSK2 and -6, it was demonstrated that HSP90 inhibition resulted in a marked decrease of the endogenous kinases in spermatids. Together, our findings demonstrate that HSP90 plays a broad and critical role in stabilization and activation of the TSSK family of protein kinases.

}, keywords = {Animals, Cercopithecus aethiops, COS Cells, Enzyme Stability, Fertility, HSP90 Heat-Shock Proteins, Humans, Male, Mice, Mice, Mutant Strains, Proteasome Endopeptidase Complex, Protein Kinase Inhibitors, Protein-Serine-Threonine Kinases, Proteolysis, Spermatids, Ubiquitination}, author = {Jha, Kula N and Coleman, Alyssa R and Wong, Lily and Salicioni, Ana M and Howcroft, Elizabeth and Johnson, Gibbes R} }