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Zeb1 的一个无编码点突变导致 Twirler 小鼠多种发育畸形和肥胖。

A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice.

机构信息

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Maryland, United States of America.

出版信息

PLoS Genet. 2011 Sep;7(9):e1002307. doi: 10.1371/journal.pgen.1002307. Epub 2011 Sep 29.

Abstract

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.

摘要

杂合 Twirler (Tw) 小鼠表现出肥胖和转圈行为,与内耳畸形有关,而纯合 Tw 小鼠则有腭裂,并在出生后不久死亡。Zeb1 是一种锌指蛋白,通过抑制其表达定义上皮细胞身份的基因,从而有助于间充质细胞命运。这个发育途径在内耳的 Tw/Tw 小鼠中被破坏。我们研究的目的是全面描述 Twirler 表型,并确定致病突变。Tw/+ 内耳表型包括半规管不规则、前庭耳石异常、耳蜗管缩短和听力损失,而 Tw/Tw 耳朵严重畸形,几乎无法识别解剖结构。Tw/+ 小鼠肥胖,伴有胰岛素抵抗和淋巴器官发育不良。我们在 Zeb1 (Zeb1(Tw)) 的 Tw 等位基因的第一个内含子中发现了一个非编码核苷酸替换,c.58+181G>A。c.58+181G>A 的敲入小鼠模型重现了 Tw 表型,而野生型敲入对照则没有,这证实了该突变是致病的。c.58+181G>A 不影响剪接,但破坏了预测的 Myb 蛋白结合位点,我们在体外证实了这一点。相比之下,Zeb1 外显子 1 靶向缺失的纯合子,Zeb1(ΔEx1),与 Tw 小鼠的侧半规管的细微异常有关。E13.5 Twirler 和 Zeb1(ΔEx1) 耳朵的表达分析证实,Zeb1(ΔEx1) 是一个无效等位基因,而 Zeb1(Tw) RNA 的表达水平比野生型 Zeb1 升高。我们得出结论,Zeb1 的非编码点突变通过获得功能作用,破坏了 Zeb1(Tw) 表达、上皮-间充质细胞命运或相互作用以及 Twirler 小鼠内耳结构发育的调节。这是导致听力或平衡障碍的一种新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88a5/3183090/b6152696bd55/pgen.1002307.g001.jpg

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