Your browser doesn't support javascript.
loading
CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4.
Garrett, Andrew M; Bosch, Peter J; Steffen, David M; Fuller, Leah C; Marcucci, Charles G; Koch, Alexis A; Bais, Preeti; Weiner, Joshua A; Burgess, Robert W.
Afiliação
  • Garrett AM; Department of Pharmacology and Department of Ophthalmology, Visual, and Anatomical Sciences, Wayne State University, Detroit, Michigan, United States of America.
  • Bosch PJ; The Jackson Laboratory, Bar Harbor, Maine, United States of America.
  • Steffen DM; Department of Biology and Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States of America.
  • Fuller LC; Department of Biology and Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States of America.
  • Marcucci CG; Department of Biology and Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States of America.
  • Koch AA; Department of Biology and Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States of America.
  • Bais P; Department of Pharmacology and Department of Ophthalmology, Visual, and Anatomical Sciences, Wayne State University, Detroit, Michigan, United States of America.
  • Weiner JA; The Jackson Laboratory, Bar Harbor, Maine, United States of America.
  • Burgess RW; Department of Biology and Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States of America.
PLoS Genet ; 15(12): e1008554, 2019 12.
Article em En | MEDLINE | ID: mdl-31877124
ABSTRACT
The mammalian Pcdhg gene cluster encodes a family of 22 cell adhesion molecules, the gamma-Protocadherins (γ-Pcdhs), critical for neuronal survival and neural circuit formation. The extent to which isoform diversity-a γ-Pcdh hallmark-is required for their functions remains unclear. We used a CRISPR/Cas9 approach to reduce isoform diversity, targeting each Pcdhg variable exon with pooled sgRNAs to generate an allelic series of 26 mouse lines with 1 to 21 isoforms disrupted via discrete indels at guide sites and/or larger deletions/rearrangements. Analysis of 5 mutant lines indicates that postnatal viability and neuronal survival do not require isoform diversity. Surprisingly, given reports that it might not independently engage in trans-interactions, we find that γC4, encoded by Pcdhgc4, is the only critical isoform. Because the human orthologue is the only PCDHG gene constrained in humans, our results indicate a conserved γC4 function that likely involves distinct molecular mechanisms.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Processamento Alternativo / Mutação / Neurônios Limite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Processamento Alternativo / Mutação / Neurônios Limite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos