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.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] A new ENU induced type II diabetes mouse mutant IGT1
    Goldsworthy, M
    Toye, A
    Eley, L
    Bentley, L
    Hough, T
    Nolan, P
    Peters, J
    Vizor, L
    Moir, L
    Ritson, D
    McNaughton, J
    Spurr, N
    Hunter, J
    Brown, SDM
    Cox, RD
    DIABETES, 2001, 50 : A238 - A238
  • [2] Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit
    Traka, Maria
    Seburn, Kevin L.
    Popko, Brian
    MAMMALIAN GENOME, 2006, 17 (09) : 950 - 955
  • [3] Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit
    Maria Traka
    Kevin L. Seburn
    Brian Popko
    Mammalian Genome, 2006, 17 : 950 - 955
  • [4] Expression of type II collagen mRNAs in developing mouse eyes and the eyes of transgenic mice harboring a deletion mutation in the pro alpha 1(II) collagen chain
    Ihanamaki, T
    Savontaus, M
    Metsaranta, M
    Vuorio, E
    Sandberg, M
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1996, 37 (03) : 1502 - 1502
  • [5] Identification through ENU genome-wide mutagenesis of a novel mutant mouse that lacks MHC-II as a result of missense mutation in SFX-5
    Chen, Yi-Ting
    Chang, Mei-Ling
    Tan, Sih-Hui
    Kung, John
    FASEB JOURNAL, 2008, 22
  • [6] DMM (DISPROPORTIONATE MICROMELIA) MUTATION IN THE MOUSE - IS THIS A DEFECT IN TYPE-II COLLAGEN
    ROARK, EF
    KOCHHAR, DM
    BARRACH, HJ
    JOURNAL OF CELL BIOLOGY, 1986, 103 (05): : A387 - A387
  • [7] EXCLUSION OF THE ALPHA-1 (II) COLLAGEN GENE AS THE MUTANT LOCUS IN TYPE-II EHLERS-DANLOS SYNDROME
    WORDSWORTH, P
    OGILVIE, D
    SYKES, B
    SMITH, R
    BRITISH JOURNAL OF RHEUMATOLOGY, 1985, 24 (01): : 111 - 112
  • [8] Expression of mutant type II collagen results in structural abnormalities in mouse eyes.
    Savontaus, M
    Ihanamaki, T
    Metsaranta, M
    Vuorio, E
    SandbergLall, M
    MATRIX BIOLOGY, 1996, 15 (03) : 175 - 176
  • [9] bfb, a Novel ENU-Induced blebs Mutant Resulting from a Missense Mutation in Fras1
    Miller, Kerry A.
    Gordon, Christopher T.
    Welfare, Megan F.
    Caruana, Georgina
    Bertram, John F.
    Bateman, John F.
    Farlie, Peter G.
    PLOS ONE, 2013, 8 (10):
  • [10] EXCLUSION OF THE ALPHA-1-(II) COLLAGEN STRUCTURAL GENE AS THE MUTANT LOCUS IN TYPE-II EHLERS-DANLOS SYNDROME
    WORDSWORTH, P
    OGILVIE, D
    SMITH, R
    SYKES, B
    ANNALS OF THE RHEUMATIC DISEASES, 1985, 44 (07) : 431 - 433