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Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development.
Snedeker, John; Schock, Elizabeth N; Struve, Jamie N; Chang, Ching-Fang; Cionni, Megan; Tran, Pamela V; Brugmann, Samantha A; Stottmann, Rolf W.
Afiliação
  • Snedeker J; Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Schock EN; Division of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Struve JN; Division of Plastic Surgery, Department of Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Chang CF; Division of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Cionni M; Division of Plastic Surgery, Department of Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Tran PV; Division of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Brugmann SA; Division of Plastic Surgery, Department of Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
  • Stottmann RW; Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
PLoS One ; 12(3): e0173258, 2017.
Article em En | MEDLINE | ID: mdl-28291836
ABSTRACT
Primary cilia are organelles extended from virtually all cells and are required for the proper regulation of a number of canonical developmental pathways. The role in cortical development of proteins important for ciliary form and function is a relatively understudied area. Here we have taken a genetic approach to define the role in forebrain development of three intraflagellar transport proteins known to be important for primary cilia function. We have genetically ablated Kif3a, Ift88, and Ttc21b in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b cortical phenotype is not due to the activity of Ttc21b within the brain itself. Secondly, some of the most striking phenotypes are from ablations in the neural crest cells and the adjacent surface ectoderm indicating that cilia transduce critical tissue-tissue interactions in the developing embryonic head. Finally, we note striking differences in phenotypes from ablations only one embryonic day apart, indicating very discrete spatiotemporal requirements for these three genes in cortical development.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transporte Biológico / Cílios / Prosencéfalo / Cinesinas / Proteínas Supressoras de Tumor / Proteínas Adaptadoras de Transdução de Sinal Limite: Animals Idioma: En Revista: PLoS One Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transporte Biológico / Cílios / Prosencéfalo / Cinesinas / Proteínas Supressoras de Tumor / Proteínas Adaptadoras de Transdução de Sinal Limite: Animals Idioma: En Revista: PLoS One Ano de publicação: 2017 Tipo de documento: Article