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Inactivation of growth differentiation factor 9 blocks folliculogenesis in pigs†.
Chen, Paula R; Uh, Kyungjun; Monarch, Kaylynn; Spate, Lee D; Reese, Emily D; Prather, Randall S; Lee, Kiho.
Afiliación
  • Chen PR; United States Department of Agriculture-Agricultural Research Service, Plant Genetics Research Unit, Columbia, MO, USA.
  • Uh K; Division of Animal Sciences, University of Missouri, Columbia, MO, USA.
  • Monarch K; Division of Animal Sciences, University of Missouri, Columbia, MO, USA.
  • Spate LD; Division of Animal Sciences, University of Missouri, Columbia, MO, USA.
  • Reese ED; National Swine Resource and Research Center, University of Missouri, Columbia, MO, USA.
  • Prather RS; Division of Animal Sciences, University of Missouri, Columbia, MO, USA.
  • Lee K; Division of Animal Sciences, University of Missouri, Columbia, MO, USA.
Biol Reprod ; 108(4): 611-618, 2023 04 11.
Article en En | MEDLINE | ID: mdl-36648449
Growth differentiation factor 9 (GDF9) is a secreted protein belonging to the transforming growth factor beta superfamily and has been well characterized for its role during folliculogenesis in the ovary. Although previous studies in mice and sheep have shown that mutations in GDF9 disrupt follicular progression, the exact role of GDF9 in pigs has yet to be elucidated. The objective of this study was to understand the role of GDF9 in ovarian function by rapidly generating GDF9 knockout (GDF9-/-) pigs by using the CRISPR/Cas9 system. Three single-guide RNAs designed to disrupt porcine GDF9 were injected with Cas9 mRNA into zygotes, and blastocyst-stage embryos were transferred into surrogates. One pregnancy was sacrificed on day 100 of gestation to investigate the role of GDF9 during oogenesis. Four female fetuses were recovered with one predicted to be GDF9-/- and the others with in-frame mutations. All four had fully formed oocytes within primordial follicles, confirming that knockout of GDF9 does not disrupt oogenesis. Four GDF9 mutant gilts were generated and were grown past puberty. One gilt was predicted to completely lack functional GDF9 (GDF9-/-), and the gilt never demonstrated standing estrus and had a severely underdeveloped reproductive tract with large ovarian cysts. Further examination revealed that the follicles from the GDF9-/- gilt did not progress past preantral stages, and the uterine vasculature was less extensive than the control pigs. By using the CRISPR/Cas9 system, we demonstrated that GDF9 is a critical growth factor for proper ovarian development and function in pigs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor 9 de Diferenciación de Crecimiento / Folículo Ovárico Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biol Reprod Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor 9 de Diferenciación de Crecimiento / Folículo Ovárico Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biol Reprod Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos