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首页> 外文期刊>Human Molecular Genetics >Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.

机译:Usherin,IIA型Usher综合征中的缺陷蛋白,很可能是内耳感觉细胞中的间质踝关节的组成部分。

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Usher syndrome type IIa (USH2A) combines moderate to severe congenital hearing impairment and retinitis pigmentosa. It is the most common genetic form of USH. USH2A encodes usherin, which was previously defined as a basement membrane protein. A much larger USH2A transcript predicted to encode a transmembrane (TM) isoform was recently reported. Here, we address the role of TM usherin in the inner ear. Analysis of the usherin alternative transcripts in the murine inner ear revealed the existence of several predicted TM usherin isoforms with modular ectodomains of different lengths. In addition, we identified in the usherin cytoplasmic region a predicted 24 amino acid peptide, derived from a newly defined exon that is predominantly expressed in the inner ear but not in the retina. In mouse and rat inner ears, we show that TM usherin is present at the base of the differentiating stereocilia, which make up the mechanosensitive hair bundles receptive to sound. The usherin immunolabeling is transient in the hair bundles of cochlear hair cells (HCs), but persists in mature hair bundles of vestibular HCs. Several lines of evidence support the involvement of TM usherin in the composition of the ankle links, a subset of filamentous lateral links connecting stereocilia at the base. By co-immunoprecipitation and in vitro binding assays, we establish that the usherin cytodomain can bind to whirlin and harmonin, two PDZ domain-containing proteins that are defective in genetic forms of isolated deafness and USH type I, respectively. These PDZ proteins are suitable to provide the anchoring of interstereocilia lateral links to the F-actin core of stereocilia. Our results strongly suggest that congenital deafness in USH type I and type II shares similar pathogenic mechanisms, i.e. the disruption of hair bundle links-mediated adhesion forces that are essential for the proper organization of growing hair bundles.
机译:IIa型Usher综合征(USH2A)合并了中度至重度先天性听力障碍和色素性视网膜炎。它是USH最常见的遗传形式。 USH2A编码usherin,以前被定义为基底膜蛋白。最近报道了预测编码跨膜(TM)同工型的更大的USH2A转录物。在这里,我们讨论TM角蛋白在内耳中的作用。小鼠内耳中的herherin替代转录本的分析表明存在几种预测的TM usherin同工型,具有不同长度的模块化胞外域。此外,我们在髓鞘细胞质区域中鉴定了一个预测的24个氨基酸的肽段,该肽段来自新定义的外显子,该外显子主要在内耳而不在视网膜中表达。在小鼠和大鼠的内耳中,我们显示出TM usherin存在于区分性纤毛的基部,该纤毛构成了对声音敏感的机械敏感发束。 Usherin免疫标记在耳蜗毛细胞(HCs)的发束中是短暂的,但在前庭HCs的成熟发束中持续存在。有几条证据支持TM角膜上皮细胞粘附素参与踝关节的构成,踝关节是在基部连接立体纤毛的丝状侧向链接的子集。通过共同免疫沉淀和体外结合测定,我们建立了herherin细胞结构域可以与whirlin和harmonin结合,这两个PDZ域包含蛋白分别在分离性耳聋和USH I型的遗传形式上有缺陷。这些PDZ蛋白适合于将胞内间侧向链锚定到纤毛的F-肌动蛋白核心。我们的结果强烈表明,USH I型和II型先天性耳聋具有相似的致病机制,即破坏发束链接介导的粘附力,这对于正常生长的发束至关重要。

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