An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

被引:241
作者
Lewis, Morag A. [1 ]
Quint, Elizabeth [2 ]
Glazier, Anne M. [1 ]
Fuchs, Helmut [3 ]
De Angelis, Martin Hrabe [3 ]
Langford, Cordelia [1 ]
van Dongen, Stijn [1 ]
Abreu-Goodger, Cei [1 ]
Piipari, Matias [1 ]
Redshaw, Nick [4 ]
Dalmay, Tamas [4 ]
Angel Moreno-Pelayo, Miguel [5 ,6 ]
Enright, Anton J.
Steel, Karen P. [1 ,2 ]
机构
[1] Wellcome Trust Sanger Inst, Hinxton, England
[2] Inst Hearing Res, MRC, Nottingham, England
[3] GSF Natl Res Ctr Environm & Hlth, Munich, Germany
[4] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[5] Hosp Ramon & Cajal, Unidad Genet Mol, E-28034 Madrid, Spain
[6] ISCIII, CIBERER, Madrid, Spain
基金
英国医学研究理事会; 英国惠康基金;
关键词
OUTER HAIR CELL; INNER-EAR; STEREOCILIA DEFECTS; MICRORNA TARGETS; GENE-EXPRESSION; MUTANT MICE; MOUSE; DIFFERENTIATION; ORGAN; IMPAIRMENT;
D O I
10.1038/ng.369
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Progressive hearing loss is common in the human population, but little is known about the molecular basis. We report a new N-ethyl-N-nitrosurea (ENU)-induced mouse mutant, diminuendo, with a single base change in the seed region of Mirn96. Heterozygotes show progressive loss of hearing and hair cell anomalies, whereas homozygotes have no cochlear responses. Most microRNAs are believed to downregulate target genes by binding to specific sites on their mRNAs, so mutation of the seed should lead to target gene upregulation. Microarray analysis revealed 96 transcripts with significantly altered expression in homozygotes; notably, Slc26a5, Ocm, Gfi1, Ptprq and Pitpnm1 were downregulated. Hypergeometric P-value analysis showed that hundreds of genes were upregulated in mutants. Different genes, with target sites complementary to the mutant seed, were downregulated. This is the first microRNA found associated with deafness, and diminuendo represents a model for understanding and potentially moderating progressive hair cell degeneration in hearing loss more generally.
引用
收藏
页码:614 / 618
页数:5
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