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非洲爪蟾内耳中表达基因的鉴定。

Identification of genes expressed in the Xenopus inner ear.

作者信息

Serrano E E, Trujillo-Provencio C, Sultemeier D R, Bullock W M, Quick Q A

机构信息

Department of Biology, New Mexico State University, Las Cruces 88003, USA.

出版信息

Cell Mol Biol (Noisy-le-grand). 2001 Nov;47(7):1229-39.

Abstract

Recent studies indicate that hearing loss in humans has strong hereditary components associated with expression of specific genes in the auditory apparatus of the inner ear. However, the inner ear poses challenges for molecular research because the amount of tissue that can be isolated is limited, and extraction procedures yield small quantities of RNA and protein. To begin to identity genes essential for auditory function, we synthesized a cDNA library using an RT-PCR protocol and total RNA isolated from eight Xenopus laevis inner ears. Sequence analysis of randomly selected clones demonstrated expression of both identified (calmodulin, SNARE protein, syndecan-2) and unidentified genes, and confirmed synthesis of full length transcripts. Confocal and scanning electron microscopy (SEM) were used to examine the structure of inner ear organs that serve as auditory receptors in amphibians: the sacculus, the amphibian papilla and the basilar papilla. SEM images illustrate the heterogeneity of bundle morphology and demonstrate the continuous appearance of stereociliary bundles in the X. laevis amphibian papilla during larval development and adult life. Investigations of gene expression in Xenopus auditory organs using clones recovered from inner ear cDNA libraries should provide insight regarding the molecular basis of hearing.

摘要

最近的研究表明,人类听力损失具有很强的遗传成分,与内耳听觉器官中特定基因的表达有关。然而,内耳给分子研究带来了挑战,因为可分离的组织量有限,而且提取程序只能获得少量的RNA和蛋白质。为了开始鉴定对听觉功能至关重要的基因,我们使用RT-PCR方案和从八个非洲爪蟾内耳分离的总RNA合成了一个cDNA文库。对随机选择的克隆进行序列分析,结果显示已鉴定基因(钙调蛋白、SNARE蛋白、多功能蛋白聚糖-2)和未鉴定基因均有表达,并证实了全长转录本的合成。共聚焦显微镜和扫描电子显微镜(SEM)被用于检查两栖动物中作为听觉感受器的内耳器官的结构:球囊、两栖乳头和基底乳头。SEM图像显示了束状形态的异质性,并证明了非洲爪蟾两栖乳头中静纤毛束在幼体发育和成体生活期间持续出现。利用从内耳cDNA文库中获得的克隆对非洲爪蟾听觉器官中的基因表达进行研究,应该能够为听力的分子基础提供深入了解。

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