The Mouse MC13 Mutant Is a Novel ENU Mutation in Collagen Type II, Alpha 1

被引:1
|
作者
Cionni, Megan [1 ]
Menke, Chelsea [1 ]
Stottmann, Rolf W. [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Div Human Genet, Cincinnati, OH 45229 USA
[2] Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Div Dev Biol, Cincinnati, OH 45229 USA
来源
PLOS ONE | 2014年 / 9卷 / 12期
基金
美国国家卫生研究院;
关键词
STICKLER SYNDROME ARTHROOPHTHALMOPATHY; COL2A1; GENE; PROCOLLAGEN COL2A1; TRANSGENIC MICE; PHENOTYPE; SCREEN; INACTIVATION; MUTAGENESIS; CODON;
D O I
10.1371/journal.pone.0116104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Phenotype-driven mutagenesis experiments are a powerful approach to identifying novel alleles in a variety of contexts. The traditional disadvantage of this approach has been the subsequent task of identifying the affected locus in the mutants of interest. Recent advances in bioinformatics and sequencing have reduced the burden of cloning these ENU mutants. Here we report our experience with an ENU mutagenesis experiment and the rapid identification of a mutation in a previously known gene. A combination of mapping the mutation with a high-density SNP panel and a candidate gene approach has identified a mutation in collagen type II, alpha I (Col2a1). Col2a1 has previously been studied in the mouse and our mutant phenotype closely resembles mutations made in the Col2a1 locus.
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页数:9
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