PLoS genetics · 2011
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice.
СтатьяResearch Support, N.I.H., IntramuralПоддержка службы здравоохранения СШАНазвание и аннотация: Перевод в очереди
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Kurima Kiyoto, Hertzano Ronna, Gavrilova Oksana, Monahan Kelly, Shpargel Karl B, Nadaraja Garani, Kawashima Yoshiyuki, Lee Kyu Yup, Ito Taku, Higashi Yujiro, Eisenman David J, Strome Scott E, Griffith Andrew J
Аннотация
Heterozygous Twirler (Tw) mice develop obesity and circling behavior associated with malformations of the inner ear, whereas homozygous Tw mice have cleft palate and die shortly after birth. Zeb1 is a zinc finger protein that contributes to mesenchymal cell fate by repression of genes whose expression defines epithelial cell identity. This developmental pathway is disrupted in inner ears of Tw/Tw mice. The purpose of our study was to comprehensively characterize the Twirler phenotype and to identify the causative mutation. The Tw/+ inner ear phenotype includes irregularities of the semicircular canals, abnormal utricular otoconia, a shortened cochlear duct, and hearing loss, whereas Tw/Tw ears are severely malformed with barely recognizable anatomy. Tw/+ mice have obesity associated with insulin-resistance and have lymphoid organ hypoplasia. We identified a noncoding nucleotide substitution, c.58+181G>A, in the first intron of the Tw allele of Zeb1 (Zeb1(Tw)). A knockin mouse model of c.58+181G>A recapitulated the Tw phenotype, whereas a wild-type knockin control did not, confirming the mutation as pathogenic. c.58+181G>A does not affect splicing but disrupts a predicted site for Myb protein binding, which we confirmed in vitro. In comparison, homozygosity for a targeted deletion of exon 1 of mouse Zeb1, Zeb1(ΔEx1), is associated with a subtle abnormality of the lateral semicircular canal that is different than those in Tw mice. Expression analyses of E13.5 Twirler and Zeb1(ΔEx1) ears confirm that Zeb1(ΔEx1) is a null allele, whereas Zeb1(Tw) RNA is expressed at increased levels in comparison to wild-type Zeb1. We conclude that a noncoding point mutation of Zeb1 acts via a gain-of-function to disrupt regulation of Zeb1(Tw) expression, epithelial-mesenchymal cell fate or interactions, and structural development of the inner ear in Twirler mice. This is a novel mechanism underlying disorders of hearing or balance.
Предметные рубрики MeSH
Abnormalities, MultipleAnimalsBinding SitesCarrier ProteinsChromosome MappingDNA-Binding ProteinsEar, InnerEpithelial-Mesenchymal TransitionGene Expression Regulation, DevelopmentalGene Knock-In TechniquesHomeodomain ProteinsIntronsKruppel-Like Transcription FactorsMiceMice, Inbred C57BLNuclear ProteinsObesityPhenotypePoint MutationRNA, UntranslatedRNA-Binding ProteinsTranscription FactorsZinc Finger E-box-Binding Homeobox 1