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A Wagener Institute for Animal Sciences, Humboldt-University, Berlin, Germany
Leibniz-Institute for Zoo and Wildlife Research, PF 601103, D-10252 Berlin, Germany
Institute for Veterinary Biochemistry, Free University, Berlin, Germany

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J Fickel Institute for Animal Sciences, Humboldt-University, Berlin, Germany
Leibniz-Institute for Zoo and Wildlife Research, PF 601103, D-10252 Berlin, Germany
Institute for Veterinary Biochemistry, Free University, Berlin, Germany

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J Schön Institute for Animal Sciences, Humboldt-University, Berlin, Germany
Leibniz-Institute for Zoo and Wildlife Research, PF 601103, D-10252 Berlin, Germany
Institute for Veterinary Biochemistry, Free University, Berlin, Germany

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A Fritzenkötter Institute for Animal Sciences, Humboldt-University, Berlin, Germany
Leibniz-Institute for Zoo and Wildlife Research, PF 601103, D-10252 Berlin, Germany
Institute for Veterinary Biochemistry, Free University, Berlin, Germany

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F Göritz Institute for Animal Sciences, Humboldt-University, Berlin, Germany
Leibniz-Institute for Zoo and Wildlife Research, PF 601103, D-10252 Berlin, Germany
Institute for Veterinary Biochemistry, Free University, Berlin, Germany

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S Blottner Institute for Animal Sciences, Humboldt-University, Berlin, Germany
Leibniz-Institute for Zoo and Wildlife Research, PF 601103, D-10252 Berlin, Germany
Institute for Veterinary Biochemistry, Free University, Berlin, Germany

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Adult roe deer males show hormonally controlled seasonal cycles of testicular growth and involution. Mediation of endocrine signals likely requires variable production of testicular growth factors for regulation of testis function. Here we studied the expression pattern of transforming growth factors (TGFs) β1 and β3. Total RNA from testis parenchyma was extracted monthly and analysed using quantitative reverse transcriptase PCR. The localization of mRNAs was determined by in situ hybridization, and corresponding proteins were visualized immunohistochemically. Both factors showed different expression levels and different seasonal expression patterns. The TGF-β1 mRNA content was up to 45 times higher than that of TGF-β3. Compared with its lowest level in May, TGF-β1 expression was slightly enhanced during pre-rut (June/July). TGF-β3 expression increased 5-fold from April to June/July and decreased thereafter to its low in December. This corresponded with changing numbers of spermatocytes and round spermatids, in which both TGF-β3 mRNA and the protein were mainly localized. The TGF-β1 mRNA was found in interstitial cells, mainly during the non-breeding season, but also in spermatocytes and spermatids during activated spermatogenesis. The translation product was localized in few spermatogenic cells only. The results suggest that TGF-β1 and -β3 are important in regulating seasonal spermatogenesis of roe deer with diverse functions affecting interstitial and spermatogenic cells.

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