TY - JOUR
T1 - Expression of the DMRT gene and its roles in early gonadal development of the Japanese pufferfish Takifugu rubripes
AU - Yamaguchi, Akihiko
AU - Lee, Kyung Hoon
AU - Fujimoto, Hiromi
AU - Kadomura, Kazushi
AU - Yasumoto, Susumu
AU - Matsuyama, Michiya
N1 - Funding Information:
We thank Drs. T. Kobayashi and T. Yoshimatsu (National Research Institute of Aquaculture, Fisheries Research Agency) for their technical advice about in situ hybridization (T. K.) or about keeping pufferfish (T. Y.), respectively. We also thank Y. Tsukashima (Nagasaki Prefectural Fisheries Co., Ltd) for providing pufferfish fertilized eggs. This work was supported in part by grant for A.Y. sponsored by Kyushu University Foundation, Sanyo Broadcasting Foundation and Grant-Aid for Scientific Research from the Japan Society for the Promotion of Science.
PY - 2006/3
Y1 - 2006/3
N2 - DMRT1, a gene containing the Doublesex/Mab-3 DNA-binding motif (DM domain), encodes a transcription factor that regulates early differentiation of Sertoli cells in the testes of vertebrates. Here, we describe the pattern of expression of six DMRT genes (DMRT1, 2a, 2b, 3, 4, and 5) during gonadal development in the Japanese pufferfish, Takifugu rubripes, for the first time. Conventional histological analysis showed that a primordial gonad is present 2 weeks after hatching and that sexual differentiation had occurred by 6 weeks after hatching, as determined by the formation of cavities in the ovaries. RT-PCR analysis showed that the DMRT1 transcript was abundant in the testes, but not in the ovaries, of 3-month-old fish. DMRT3 transcript was also detected in the testes, but not in the ovaries, indicating that the patterns of gonadal expression of DMRT3 are very similar to DMRT1. The other four DMRT genes examined did not exhibit sex-specific expression patterns. In situ hybridization analysis revealed that, after gonadal differentiation was complete, DMRT1 was expressed in the Sertoli cells that were in proximity to proliferating spermatogonia. These results indicate that DMRT1 involved in gonadal development rather than sex differentiation and that its expression correlates with the proliferation of spermatogonia in T. rubripes. The expression profile of DMRT1 in T. rubripes was similar to that in the teleost species Medaka.
AB - DMRT1, a gene containing the Doublesex/Mab-3 DNA-binding motif (DM domain), encodes a transcription factor that regulates early differentiation of Sertoli cells in the testes of vertebrates. Here, we describe the pattern of expression of six DMRT genes (DMRT1, 2a, 2b, 3, 4, and 5) during gonadal development in the Japanese pufferfish, Takifugu rubripes, for the first time. Conventional histological analysis showed that a primordial gonad is present 2 weeks after hatching and that sexual differentiation had occurred by 6 weeks after hatching, as determined by the formation of cavities in the ovaries. RT-PCR analysis showed that the DMRT1 transcript was abundant in the testes, but not in the ovaries, of 3-month-old fish. DMRT3 transcript was also detected in the testes, but not in the ovaries, indicating that the patterns of gonadal expression of DMRT3 are very similar to DMRT1. The other four DMRT genes examined did not exhibit sex-specific expression patterns. In situ hybridization analysis revealed that, after gonadal differentiation was complete, DMRT1 was expressed in the Sertoli cells that were in proximity to proliferating spermatogonia. These results indicate that DMRT1 involved in gonadal development rather than sex differentiation and that its expression correlates with the proliferation of spermatogonia in T. rubripes. The expression profile of DMRT1 in T. rubripes was similar to that in the teleost species Medaka.
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U2 - 10.1016/j.cbd.2005.08.003
DO - 10.1016/j.cbd.2005.08.003
M3 - Article
C2 - 20483235
AN - SCOPUS:33644552405
SN - 1744-117X
VL - 1
SP - 59
EP - 68
JO - Comparative Biochemistry and Physiology - Part D: Genomics and Proteomics
JF - Comparative Biochemistry and Physiology - Part D: Genomics and Proteomics
IS - 1 SPEC. ISS.
ER -