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Ovol2, a zinc finger transcription factor, is dispensable for spermatogenesis in mice.
Zhang, Jin; Dong, Juan; Qin, Weibing; Cao, Congcong; Wen, Yujiao; Tang, Yunge; Yuan, Shuiqiao.
Afiliación
  • Zhang J; Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
  • Dong J; College of Animal Science and Technology, Northwest A&F University, Yangling, People's Republic of China.
  • Qin W; Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
  • Cao C; NHC Key Laboratory of Male Reproduction and Genetics, Family Planning Research Institute of Guangdong Province, Guangzhou, People's Republic of China.
  • Wen Y; Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
  • Tang Y; Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
  • Yuan S; NHC Key Laboratory of Male Reproduction and Genetics, Family Planning Research Institute of Guangdong Province, Guangzhou, People's Republic of China. tyg813@126.com.
Reprod Biol Endocrinol ; 17(1): 98, 2019 Nov 23.
Article en En | MEDLINE | ID: mdl-31759386
ABSTRACT
Ovol2, a mouse homolog of Drosophila ovo, was identified as a zinc finger transcription factor predominantly expressed in testis. However, the function of Ovol2 in postnatal male germ cell development remains enigmatic. Here, we firstly examined the mRNA and protein levels of Ovol2 in developing mouse testes by RT-qPCR and western blot and found that both mRNA and protein of Ovol2 are continually expressed in postnatal developing testes from postnatal day 0 (P0) testes to adult testes (P56) and exhibits its higher level at adult testis. Further testicular immuno-staining revealed that OVOL2 is highly expressed in the spermatogonia, spermatocytes and round spermatids. Interestingly, our conditional ovol2 knockout mouse model show that loss of ovol2 in embryonic germ cells does not affect fecundity in mice. Our data also show that Ovol1 may have compensated for the loss of Ovol2 functions in germ cells. Overall, our data indicate that ovol2 is dispensable for germ cell development and spermatogenesis.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espermatogénesis / Testículo / Factores de Transcripción / Dedos de Zinc Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Reprod Biol Endocrinol Asunto de la revista: ENDOCRINOLOGIA / MEDICINA REPRODUTIVA Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espermatogénesis / Testículo / Factores de Transcripción / Dedos de Zinc Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Reprod Biol Endocrinol Asunto de la revista: ENDOCRINOLOGIA / MEDICINA REPRODUTIVA Año: 2019 Tipo del documento: Article