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非洲爪蟾内耳转录组的RNA测序和微阵列分析揭示了用于遗传性听力和平衡障碍的直系同源OMIM(®)基因。

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance.

作者信息

Ramírez-Gordillo Daniel, Powers TuShun R, van Velkinburgh Jennifer C, Trujillo-Provencio Casilda, Schilkey Faye, Serrano Elba E

机构信息

Biology Department, New Mexico State University (NMSU), Las Cruces, NM, 88003, USA.

National Center for Genome Resources (NCGR), Santa Fe, NM, 87505, USA.

出版信息

BMC Res Notes. 2015 Nov 18;8:691. doi: 10.1186/s13104-015-1485-1.

Abstract

BACKGROUND

Auditory and vestibular disorders are prevalent sensory disabilities caused by genetic and environmental (noise, trauma, chemicals) factors that often damage mechanosensory hair cells of the inner ear. Development of treatments for inner ear disorders of hearing and balance relies on the use of animal models such as fish, amphibians, reptiles, birds, and non-human mammals. Here, we aimed to augment the utility of the genus Xenopus for uncovering genetic mechanisms essential for the maintenance of inner ear structure and function.

RESULTS

Using Affymetrix GeneChip(®) X. laevis Genome 2.0 Arrays and Illumina-Solexa sequencing methods, we determined that the transcriptional profile of the Xenopus laevis inner ear comprises hundreds of genes that are orthologous to OMIM(®) genes implicated in deafness and vestibular disorders in humans. Analysis of genes that mapped to both technologies demonstrated that, with our methods, a combination of microarray and RNA-Seq detected expression of more genes than either platform alone.

CONCLUSIONS

As part of this study we identified candidate scaffold regions of the Xenopus tropicalis genome that can be used to investigate hearing and balance using genetic and informatics procedures that are available through the National Xenopus Resource (NXR), and the open access data repository, Xenbase. The results and approaches presented here expand the viability of Xenopus as an animal model for inner ear research.

摘要

背景

听觉和前庭障碍是常见的感觉障碍,由遗传和环境(噪音、创伤、化学物质)因素引起,这些因素常常损害内耳的机械感觉毛细胞。内耳听力和平衡障碍治疗方法的开发依赖于鱼类、两栖动物、爬行动物、鸟类和非人类哺乳动物等动物模型的使用。在此,我们旨在增强非洲爪蟾属在揭示维持内耳结构和功能所必需的遗传机制方面的效用。

结果

使用Affymetrix GeneChip(®)非洲爪蟾基因组2.0阵列和Illumina-Solexa测序方法,我们确定非洲爪蟾内耳的转录谱包含数百个与人类耳聋和前庭障碍相关的OMIM(®)基因的直系同源基因。对两种技术都映射到的基因的分析表明,使用我们的方法,微阵列和RNA测序相结合检测到的基因表达比单独使用任何一个平台都多。

结论

作为本研究的一部分,我们确定了热带爪蟾基因组的候选支架区域,可通过国家爪蟾资源库(NXR)和开放获取数据存储库Xenbase提供的遗传和信息学程序来研究听力和平衡问题。此处呈现的结果和方法扩展了爪蟾作为内耳研究动物模型的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8c8/4652436/93320e30d234/13104_2015_1485_Fig1_HTML.jpg

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