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Targeted mutagenesis study reveals marked infertility and defective sperm motility in Ttll5-deficient male mice, highlighting an essential role for tubulin polyglutamylation in sperm structure.
Background: Ttll5/STAMP is a multifunctional protein in cells with unknown activity in animals. Results: Targeted disruption of the Ttll5/Stamp gene in mice causes male infertility with reduced -tubulin polyglutamylation and axoneme disruption in sperm. Conclusion: Ttll5/Stamp deficiency differs from previously described defects in sperm maturation and function. Significance: Ttll5/Stamp is a new gene involved in sperm maturation that may be relevant for human fertility. TTLL5/STAMP (tubulin tyrosine ligase-like family member 5) has multiple activities in cells. TTLL5 is one of 13 TTLLs, has polyglutamylation activity, augments the activity of p160 coactivators (SRC-1 and TIF2) in glucocorticoid receptor-regulated gene induction and repression, and displays steroid-independent growth activity with several cell types. To examine TTLL5/ STAMP functions in whole animals, mice were prepared with an internal deletion that eliminated several activities of the Stamp gene. This mutation causes both reduced levels of STAMP mRNA and C-terminal truncation of STAMP protein. Homozygous targeted mutant (Stamp tm/tm ) mice appear normal except for marked decreases in male fertility associated with defects in progressive sperm motility. Abnormal axonemal structures with loss of tubulin doublets occur in most Stamp tm/tm sperm tails in conjunction with substantial reduction in -tubulin polyglutamylation, which closely correlates with the reduction in mutant STAMP mRNA. The axonemes in other structures appear unaffected. There is no obvious change in the organs for sperm development of WT versus Stamp tm/tm males despite the levels of WT STAMP mRNA in testes being 20-fold higher than in any other organ examined. This defect in male fertility is unrelated to other Ttll genes or 24 genes previously identified as important for sperm function. Thus, STAMP appears to participate in a unique, tissue-selective TTLL-mediated pathway for -tubulin polyglutamylation that is required for sperm maturation and motility and may be relevant for male fertility.
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Lee et al. (2013) studied this question.
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