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Functional Analysis of KIT Gene Structural Mutations Causing the Porcine Dominant White Phenotype Using Genome Edited Mouse Models.


ABSTRACT: The dominant white phenotype in pigs is thought to be mainly due to a structural mutation in the KIT gene, a splice mutation (G > A) at the first base in intron 17 which leads to the deletion of exon 17 in the mature KIT mRNA. However, this hypothesis has not yet been validated by functional studies. Here, we created two mouse models, KIT D17/+ to mimic the splice mutation, and KIT Dup/+ to partially mimic the duplication mutation of KIT gene in dominant white pigs using CRISPR/Cas9 technology. We found that the splice mutation homozygote is lethal and the heterozygous mice have a piebald coat. Slightly increased expression of KIT in KIT Dup/+ mice did not confer the patched phenotype and had no obvious impact on coat color. Interestingly, the combination of these two mutations reduced the phosphorylation of PI3K and MAPK pathway associated proteins, which may be related to the impaired migration of melanoblasts observed during embryonic development that eventually leads to the dominant white phenotype.

SUBMITTER: Sun G 

PROVIDER: S-EPMC7063667 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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Functional Analysis of <i>KIT</i> Gene Structural Mutations Causing the Porcine Dominant White Phenotype Using Genome Edited Mouse Models.

Sun Guanjie G   Liang Xinyu X   Qin Ke K   Qin Yufeng Y   Shi Xuan X   Cong Peiqing P   Mo Delin D   Liu Xiaohong X   Chen Yaosheng Y   He Zuyong Z  

Frontiers in genetics 20200303


The dominant white phenotype in pigs is thought to be mainly due to a structural mutation in the <i>KIT</i> gene, a splice mutation (G > A) at the first base in intron 17 which leads to the deletion of exon 17 in the mature <i>KIT</i> mRNA. However, this hypothesis has not yet been validated by functional studies. Here, we created two mouse models, <i>KIT <sup>D17/+</sup></i> to mimic the splice mutation, and <i>KIT <sup>Dup/+</sup></i> to partially mimic the duplication mutation of <i>KIT</i> g  ...[more]

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