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Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System
Paired-homeodomain transcription factor 4 (PAX4) gene encodes a transcription factor which plays an important role in the generation, differentiation, development, and survival of insulin-producing β-cells during mammalian pancreas development. PAX4 is a key diabetes mellitus (DM) susceptibility gen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071587/ https://www.ncbi.nlm.nih.gov/pubmed/29950431 http://dx.doi.org/10.1534/g3.118.300448 |
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author | Xu, Yuanyuan Wang, Yong Song, Yuning Deng, Jichao Chen, Mao Ouyang, Hongsheng Lai, Liangxue Li, Zhanjun |
author_facet | Xu, Yuanyuan Wang, Yong Song, Yuning Deng, Jichao Chen, Mao Ouyang, Hongsheng Lai, Liangxue Li, Zhanjun |
author_sort | Xu, Yuanyuan |
collection | PubMed |
description | Paired-homeodomain transcription factor 4 (PAX4) gene encodes a transcription factor which plays an important role in the generation, differentiation, development, and survival of insulin-producing β-cells during mammalian pancreas development. PAX4 is a key diabetes mellitus (DM) susceptibility gene, which is associated with many different types of DM, including T1DM, T2DM, maturity onset diabetes of the young 9 (MODY9) and ketosis prone diabetes. In this study, a novel PAX4 gene knockout (KO) model was generated through co-injection of clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (Cas9) mRNA/sgRNA into rabbit zygotes. Typical phenotypes of growth retardation, persistent hyperglycemia, decreased number of insulin-producing β cells and increased number of glucagon-producing α cells were observed in the homozygous PAX4 KO rabbits. Furthermore, DM associated phenotypes including diabetic nephropathy, hepatopathy, myopathy and cardiomyopathy were also observed in the homozygous PAX4 KO rabbits but not in the wild type (WT) controls and the heterozygous PAX4 KO rabbits. In summary, this is the first PAX4 gene KO rabbit model generated by CRISPR/Cas9 system. This novel rabbit model may provide a new platform for function study of PAX4 gene in rabbit and gene therapy of human DM in clinical trails. |
format | Online Article Text |
id | pubmed-6071587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-60715872018-08-03 Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System Xu, Yuanyuan Wang, Yong Song, Yuning Deng, Jichao Chen, Mao Ouyang, Hongsheng Lai, Liangxue Li, Zhanjun G3 (Bethesda) Investigations Paired-homeodomain transcription factor 4 (PAX4) gene encodes a transcription factor which plays an important role in the generation, differentiation, development, and survival of insulin-producing β-cells during mammalian pancreas development. PAX4 is a key diabetes mellitus (DM) susceptibility gene, which is associated with many different types of DM, including T1DM, T2DM, maturity onset diabetes of the young 9 (MODY9) and ketosis prone diabetes. In this study, a novel PAX4 gene knockout (KO) model was generated through co-injection of clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (Cas9) mRNA/sgRNA into rabbit zygotes. Typical phenotypes of growth retardation, persistent hyperglycemia, decreased number of insulin-producing β cells and increased number of glucagon-producing α cells were observed in the homozygous PAX4 KO rabbits. Furthermore, DM associated phenotypes including diabetic nephropathy, hepatopathy, myopathy and cardiomyopathy were also observed in the homozygous PAX4 KO rabbits but not in the wild type (WT) controls and the heterozygous PAX4 KO rabbits. In summary, this is the first PAX4 gene KO rabbit model generated by CRISPR/Cas9 system. This novel rabbit model may provide a new platform for function study of PAX4 gene in rabbit and gene therapy of human DM in clinical trails. Genetics Society of America 2018-06-27 /pmc/articles/PMC6071587/ /pubmed/29950431 http://dx.doi.org/10.1534/g3.118.300448 Text en Copyright © 2018 Xu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Xu, Yuanyuan Wang, Yong Song, Yuning Deng, Jichao Chen, Mao Ouyang, Hongsheng Lai, Liangxue Li, Zhanjun Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System |
title | Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System |
title_full | Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System |
title_fullStr | Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System |
title_full_unstemmed | Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System |
title_short | Generation and Phenotype Identification of PAX4 Gene Knockout Rabbit by CRISPR/Cas9 System |
title_sort | generation and phenotype identification of pax4 gene knockout rabbit by crispr/cas9 system |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071587/ https://www.ncbi.nlm.nih.gov/pubmed/29950431 http://dx.doi.org/10.1534/g3.118.300448 |
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