Cargando…

CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4

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/...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957209/
https://www.ncbi.nlm.nih.gov/pubmed/31877124
http://dx.doi.org/10.1371/journal.pgen.1008554
_version_ 1783487278597799936
author 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.
author_facet 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.
author_sort Garrett, Andrew M.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-6957209
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-69572092020-01-26 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. PLoS Genet Research Article 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. Public Library of Science 2019-12-26 /pmc/articles/PMC6957209/ /pubmed/31877124 http://dx.doi.org/10.1371/journal.pgen.1008554 Text en © 2019 Garrett et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
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.
CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4
title CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4
title_full CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4
title_fullStr CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4
title_full_unstemmed CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4
title_short CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4
title_sort crispr/cas9 interrogation of the mouse pcdhg gene cluster reveals a crucial isoform-specific role for pcdhgc4
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957209/
https://www.ncbi.nlm.nih.gov/pubmed/31877124
http://dx.doi.org/10.1371/journal.pgen.1008554
work_keys_str_mv AT garrettandrewm crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT boschpeterj crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT steffendavidm crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT fullerleahc crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT marcuccicharlesg crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT kochalexisa crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT baispreeti crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT weinerjoshuaa crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4
AT burgessrobertw crisprcas9interrogationofthemousepcdhggeneclusterrevealsacrucialisoformspecificroleforpcdhgc4