Abstract

Male contraception is a very active area of research. Several hormonal agents have entered clinical trials, while potential non-hormonal targets have been brought to light more recently and are at earlier stages of development. The general strategy is to target genes along the molecular pathways of sperm production, maturation, or function, and it is predicted that these novel approaches will hopefully lead to more selective male contraceptive compounds with a decreased side effect burden. Protein kinases are known to play a major role in signaling events associated with sperm differentiation and function. In this review, we focus our analysis on the testis-specific serine kinase (TSSK) protein family. We have previously shown that members of the family of TSSKs are postmeiotically expressed in male germ cells and in mature mammalian sperm. The restricted postmeiotic expression of TSSKs as well as the importance of phosphorylation in signaling processes strongly suggests that TSSKs have an important role in germ cell differentiation and/or sperm function. This prediction has been supported by the reported sterile phenotype of the Tssk6 knockout (KO) mice and of the double Tssk1 and Tssk2 KO mice and by the male subfertile phenotype observed in a Tssk4 KO mouse model.

Highlights

  • The ability to control fertility through the accessibility to effective contraceptive methods is an indispensable component of preventive health

  • Defects on Izumo1 translocation are consistent with defects in actin polymerization occurring in the sperm head, which we found compromised in the absence of Tssk6

  • Evaluation of Tssk6 mRNA transcript levels as a predictor of bull sperm fertilizing ability has been proposed for use in the veterinary clinic [34]

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Summary

Introduction

The ability to control fertility through the accessibility to effective contraceptive methods is an indispensable component of preventive health. Our study provided further support to the notion that TSSK family members display different cellular localizations, pointing to sub-functionalization rather than a redundant role for these protein kinases.

Results
Conclusion
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