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Connexin mutations in deafness

耳聋中的连接蛋白突变

基本信息

批准号：
7195040
负责人：
THOMAS W WHITE
金额：
$ 25.97万
依托单位：
STATE UNIVERSITY NEW YORK STONY BROOK
依托单位国家：
美国
项目类别：
财政年份：
2004
资助国家：
美国
起止时间：
2004-04-01 至 2009-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7195040
关键词：
Alleles Amino Acid Substitution Animal Model Auditory Behavior Biological Assay Blood Circulation Cations Cell Line Cells Cochlea Code Connexins Cytoplasm Data Deletion Mutation Disease Endolymph Gap Junctions Genes Genetic Genetically Engineered Mouse Goals Hair Cells Human Imaging technology In Vitro Knock-in Mouse Labyrinth Left Link Lymph Mammalian Cell Methods Missense Mutation Modeling Monovalent Cations Movement Mus Mutation Pathology Pattern Perilymph Permeability Play Potassium Property Range Research Personnel Role Screening procedure Second Messenger Systems Sensory Hair Supporting Cell Techniques Tissues United States Variant Xenopus oocyte deafness disease-causing mutation embryonic stem cell functional loss gap junction channel hearing impairment homologous recombination human disease insight mutant patch clamp potassium ion programs second messenger small molecule tool

项目摘要

DESCRIPTION (provided by applicant): Mutations in the human connexin26 gene (Cx26, or GJB2) are the leading cause of nonsyndromic deafness in the United States. Mutations in other connexins, Cx30 (GJB6), Cx31 (GJB3), and Cx32 (GJB1) have also been linked to hearing loss in humans. While this illuminates a critical function for cochlear gap junctions, it is unclear how a common pathology can arise from mutations within different connexin genes that have an overlapping expression pattern in the inner ear, as is the case for Cx26, Cx30, Cx31 and Cx32. There are no gap junctions between the sensory hair cells in humans; but they are expressed in the supporting cells of the cochlea. The current hypothesis is that these junctions play a role in the re-circulation of potassium ions between the end lymph and perilymph. It is difficult to reconcile this model with the available data on potassium permeation through gap junction channels, as all connexins are readily permeated by this caution and the loss of a single cochlear connexin would still leave other functional connexins available to perform this task. Connexins do show differential permeability to a wide range of other small molecules and second messengers, and we hypothesize that these permeation differences are critical for cochlear function, and more difficult to compensate for following the functional loss of one of the several available channel subunits. The objective of this application is to precisely define which permeation properties of Cx26 are necessary for normal auditory function in humans. To achieve this goal, we first propose to screen mutant Cx26 alleles for functional activity in the paired Xenopus oocyte assay. Cx26 mutants that retain channel function will have their perm selectivity properties analyzed by dual patch clamp methods in transected mammalian cell lines. Finally, We will generate and characterize genetically engineered mice where the native Cx26 gene has been replaced by the functionally active human Cx26 disease causing mutations. We will use genetic knock-in techniques to generate mice that will allow us to evaluate the in vitro derived functional differences in an animal model. Contrasting the differences in permeation between wild type and disease causing variants of Cx26 will not only provide mechanistic insight into hearing loss, but will also provide a general model for the need for connexin diversity in other tissues where human disease results from mutations in connexin genes.

描述(由申请人提供)：人类连接蛋白26基因(Cx26或GJB2)突变是美国非综合征性耳聋的主要原因。其他连接蛋白Cx30(GJB6)、Cx31(GJB3)和Cx32(GJB1)的突变也与人类听力损失有关。虽然这阐明了耳蜗缝隙连接的关键功能，但尚不清楚不同连接蛋白基因的突变如何会引起常见的病理，这些基因在内耳具有重叠的表达模式，就像Cx26、Cx30、Cx31和Cx32一样。人类的感觉毛细胞之间没有缝隙连接，但它们表达在耳蜗的支持细胞中。目前的假设是，这些连接在末端淋巴和外淋巴之间的钾离子再循环中发挥了作用。很难将这一模型与有关钾通过缝隙连接通道渗透的现有数据相一致，因为所有连接蛋白都很容易被这种谨慎所渗透，而失去一个耳蜗间隙连接蛋白仍然会留下其他功能连接蛋白来执行这一任务。连接蛋白对广泛的其他小分子和第二信使确实表现出不同的通透性，我们假设这些通透性差异对耳蜗功能是关键的，并且在几个可用通道亚基之一的功能丧失后更难补偿。这项应用的目的是精确地定义Cx26的哪些渗透特性是人类正常听觉功能所必需的。为了实现这一目标，我们首先建议在非洲爪哇卵母细胞试验中筛选Cx26突变等位基因的功能活性。保留通道功能的Cx26突变体将在横断的哺乳动物细胞系中用双膜片钳方法分析其PERM选择性特性。最后，我们将产生并鉴定基因工程小鼠，在这些小鼠中，天然的Cx26基因已经被功能活跃的人类Cx26疾病取代，导致突变。我们将使用基因敲入技术来产生小鼠，这将使我们能够在动物模型中评估体外衍生的功能差异。对比Cx26野生型和致病变异体在渗透方面的差异，不仅将提供对听力损失的机械性洞察，还将为其他组织中连接蛋白多样性的需求提供一个通用模型，在这些组织中，人类疾病是由连接蛋白基因突变引起的。