Title: Expression of tubb3, a Beta-tubulin isotype, is regulated by androgens in mouse and rat sertoli cells
Authors: De Gendt, Karel ×
Denolet, Evi
Willems, Ariane
Daniƫls, Veerle
Clinckemalie, Liesbeth
Denayer, Sarah
Wilkinson, Miles F
Claessens, Frank
Swinnen, Johan
Verhoeven, Guido #
Issue Date: Nov-2011
Publisher: Society for the Study of Reproduction
Series Title: Biology of Reproduction vol:85 issue:5 pages:934-945
Abstract: Our previous analysis of Sertoli cell androgen receptor (AR) knockout (SCARKO) mice revealed that several cytoskeletal components are a potential target of androgen action. Here, we found that one of these components, the beta-tubulin isotype Tubb3, is differentially regulated in testes from SCARKO mice (relative to littermate controls) from Postnatal Day 10 to adulthood. The Tubb3 gene is unique in this respect, as at Day 10, no other beta-tubulin genes are significantly regulated by AR. We further characterized androgen regulation of Tubb3 in vivo and in vitro and demonstrated that it is a conserved feature in both mice and rats. To investigate whether androgens directly regulate Tubb3 expression, we screened for androgen response elements (AREs) in the Tubb3 gene. In silico analysis revealed the presence of four ARE motifs in Tubb3 intron 1, two of which bind to AR in vitro. Mutation of one of these (ARE1) strongly reduced androgen-dependent reporter gene expression. These results, coupled with the finding that the AR binds to the Tubb3 ARE region in vivo, suggest that Tubb3 is a direct target of AR. Our data strengthen the contention that androgens exert their effects on spermatogenesis, in part, through modulation of the Sertoli cell cytoskeleton. Androgen regulation of beta-tubulin has also been described in neurons, fortifying the already known similarity in microtubule organization in Sertoli cell processes and neurons, the only other cell type in which Tubb3 is known to be expressed.
ISSN: 0006-3363
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Molecular Endocrinology
Clinical and Experimental Endocrinology
Biochemistry Section (Medicine) (-)
Laboratory of Lipid Metabolism and Cancer (+)
× corresponding author
# (joint) last author

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