Klockars Tuomas, Perheentupa Teemu, Dahl Hans-Henrik M
Murdoch Childrens Research Institute, Department of Paediatrics, University of Melbourne, The Royal Children's Hospital, Parkville, Victoria, Australia.
J Assoc Res Otolaryngol. 2003 Mar;4(1):24-40. doi: 10.1007/s10162-002-2058-2. Epub 2002 Jun 20.
The development and function of the inner ear is complex requiring the correct and coordinated expression of many genes. The recent progress in the analyses of the human and other genomes has provided tools for identification of genes involved in hearing. As more and more nucleotide sequence information accumulates, experimental methods of molecular biology are rapidly being supplemented, and partially supplanted, by computational methods. In this study we present comprehensive in silico analyses of a cDNA library representing almost 1600 transcripts isolated from mouse inner ear. By mining the public databases we were able to rapidly and efficiently identify numerous transcripts likely to have a specific role in the auditory or vestibular function of the inner ear. Analyses revealed about 600 known genes and almost 100 inner-ear specific transcripts. Almost 50 of these are candidate genes for hearing impairment based on their chromosomal localization and inner-ear expression pattern. We describe a powerful approach to identify novel genes associated with hearing and vestibular function, further increasing our understanding of the molecular biology of the inner ear.
内耳的发育和功能十分复杂,需要众多基因正确且协调地表达。人类基因组及其他基因组分析的最新进展为鉴定参与听力的基因提供了工具。随着越来越多核苷酸序列信息的积累,分子生物学实验方法正迅速被计算方法补充,甚至部分被取代。在本研究中,我们对一个代表从鼠标内耳分离出的近1600个转录本的cDNA文库进行了全面的计算机分析。通过挖掘公共数据库,我们能够快速且高效地鉴定出众多可能在内耳听觉或前庭功能中发挥特定作用的转录本。分析揭示了约600个已知基因和近100个内耳特异性转录本。基于它们的染色体定位和内耳表达模式,其中近50个是听力障碍的候选基因。我们描述了一种强大的方法来鉴定与听力和前庭功能相关的新基因,进一步增进了我们对内耳分子生物学的理解。