Trujillo-Provencio Casilda, Powers TuShun R, Sultemeier David R, Ramirez-Gordillo Daniel, Serrano Elba E
Biology Department, New Mexico State University, Las Cruces, NM, USA.
Methods Mol Biol. 2016;1427:73-92. doi: 10.1007/978-1-4939-3615-1_5.
The amphibian Xenopus offers a unique model system for uncovering the genetic basis of auditory and vestibular function in an organism that is well-suited for experimental manipulation during animal development. However, many procedures for analyzing gene expression in the peripheral auditory and vestibular systems mandate the ability to isolate intact RNA from inner ear tissue. Methods presented here facilitate preparation of high-quality inner ear RNA from larval and post-metamorphic Xenopus specimens that can be used for a variety of purposes. We demonstrate that RNA isolated with these protocols is suitable for microarray analysis and Illumina-Solexa sequencing (RNA-Seq) of inner ear organs, and for cloning of large transcripts, such as those for ion channels. Genetic sequences cloned with these procedures can be used for transient transfection of Xenopus kidney cell lines with fluorescent protein fusion constructs.
两栖动物非洲爪蟾为揭示生物听觉和前庭功能的遗传基础提供了一个独特的模型系统,该生物非常适合在动物发育过程中进行实验操作。然而,许多用于分析外周听觉和前庭系统中基因表达的程序都要求能够从内耳组织中分离出完整的RNA。本文介绍的方法有助于从非洲爪蟾幼体和变态后的标本中制备高质量的内耳RNA,这些RNA可用于多种目的。我们证明,用这些方案分离的RNA适用于内耳器官的微阵列分析和Illumina-Solexa测序(RNA-Seq),以及用于克隆大转录本,如离子通道的转录本。用这些程序克隆的遗传序列可用于用荧光蛋白融合构建体对非洲爪蟾肾细胞系进行瞬时转染。