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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/...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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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 |
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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 |
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