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使用全转录本阵列对Igf1基因缺陷小鼠的前庭器官进行比较基因表达研究。

Comparative gene expression study of the vestibular organ of the Igf1 deficient mouse using whole-transcript arrays.

作者信息

Rodríguez-de la Rosa Lourdes, Sánchez-Calderón Hortensia, Contreras Julio, Murillo-Cuesta Silvia, Falagan Sandra, Avendaño Carlos, Dopazo Joaquín, Varela-Nieto Isabel, Milo Marta

机构信息

Neurobiology of Hearing, Department of Endocrine and Nervous System Pathophysiology, Alberto Sols Biomedical Research Institute (IIBM), CSIC-UAM, Madrid, Spain; Biomedical Research Networking Center on Rare Diseases (CIBERER), Institute of Health Carlos III (ISCIII), Madrid, Spain; IdiPAZ Institute for Health Research, Madrid, Spain.

Neurobiology of Hearing, Department of Endocrine and Nervous System Pathophysiology, Alberto Sols Biomedical Research Institute (IIBM), CSIC-UAM, Madrid, Spain.

出版信息

Hear Res. 2015 Dec;330(Pt A):62-77. doi: 10.1016/j.heares.2015.08.016. Epub 2015 Sep 1.

Abstract

The auditory and vestibular organs form the inner ear and have a common developmental origin. Insulin like growth factor 1 (IGF-1) has a central role in the development of the cochlea and maintenance of hearing. Its deficiency causes sensorineural hearing loss in man and mice. During chicken early development, IGF-1 modulates neurogenesis of the cochleovestibular ganglion but no further studies have been conducted to explore the potential role of IGF-1 in the vestibular system. In this study we have compared the whole transcriptome of the vestibular organ from wild type and Igf1(-/-) mice at different developmental and postnatal times. RNA was prepared from E18.5, P15 and P90 vestibular organs of Igf1(-/-) and Igf1(+/+) mice and the transcriptome analysed in triplicates using Affymetrix(®) Mouse Gene 1.1 ST Array Plates. These plates are whole-transcript arrays that include probes to measure both messenger (mRNA) and long intergenic non-coding RNA transcripts (lincRNA), with a coverage of over 28 thousand coding transcripts and over 7 thousands non-coding transcripts. Given the complexity of the data we used two different methods VSN-RMA and mmBGX to analyse and compare the data. This is to better evaluate the number of false positives and to quantify uncertainty of low signals. We identified a number of differentially expressed genes that we described using functional analysis and validated using RT-qPCR. The morphology of the vestibular organ did not show differences between genotypes and no evident alterations were observed in the vestibular sensory areas of the null mice. However, well-defined cellular alterations were found in the vestibular neurons with respect their number and size. Although these mice did not show a dramatic vestibular phenotype, we conducted a functional analysis on differentially expressed genes between genotypes and across time. This was with the aim to identify new pathways that are involved in the development of the vestibular organ as well as pathways that maybe affected by the lack of IGF-1 and be associated to the morphological changes of the vestibular neurons that we observed in the Igf1(-/-) mice.

摘要

听觉和前庭器官构成内耳,且有共同的发育起源。胰岛素样生长因子1(IGF-1)在耳蜗发育和听力维持中起核心作用。其缺乏会导致人类和小鼠出现感音神经性听力损失。在鸡的早期发育过程中,IGF-1调节耳蜗前庭神经节的神经发生,但尚未有进一步研究探索IGF-1在前庭系统中的潜在作用。在本研究中,我们比较了野生型和Igf1(-/-)小鼠在不同发育和出生后时期前庭器官的全转录组。从Igf1(-/-)和Igf1(+/+)小鼠的E18.5、P15和P90前庭器官中提取RNA,并使用Affymetrix(®) Mouse Gene 1.1 ST Array Plates对转录组进行三次重复分析。这些平板是全转录本阵列,包括用于测量信使核糖核酸(mRNA)和长链基因间非编码RNA转录本(lincRNA)的探针,覆盖超过2.8万个编码转录本和超过7000个非编码转录本。鉴于数据的复杂性,我们使用两种不同的方法VSN-RMA和mmBGX来分析和比较数据。这是为了更好地评估假阳性数量并量化低信号的不确定性。我们鉴定了一些差异表达基因,并通过功能分析进行描述,还使用RT-qPCR进行了验证。前庭器官的形态在不同基因型之间未显示差异,在基因敲除小鼠的前庭感觉区域也未观察到明显改变。然而,在前庭神经元的数量和大小方面发现了明确的细胞改变。尽管这些小鼠没有表现出明显的前庭表型,但我们对不同基因型之间以及不同时间的差异表达基因进行了功能分析。目的是确定参与前庭器官发育的新途径,以及可能受IGF-1缺乏影响并与我们在Igf1(-/-)小鼠中观察到 的前庭神经元形态变化相关的途径。

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