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细胞类型特异性转录组分析揭示了 Zeb1 和 miR-200b 在小鼠内耳形态发生中的主要作用。

Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis.

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, University of Maryland, Baltimore, Maryland, United States of America.

出版信息

PLoS Genet. 2011 Sep;7(9):e1002309. doi: 10.1371/journal.pgen.1002309. Epub 2011 Sep 29.

Abstract

Cellular heterogeneity hinders the extraction of functionally significant results and inference of regulatory networks from wide-scale expression profiles of complex mammalian organs. The mammalian inner ear consists of the auditory and vestibular systems that are each composed of hair cells, supporting cells, neurons, mesenchymal cells, other epithelial cells, and blood vessels. We developed a novel protocol to sort auditory and vestibular tissues of newborn mouse inner ears into their major cellular components. Transcriptome profiling of the sorted cells identified cell type-specific expression clusters. Computational analysis detected transcription factors and microRNAs that play key roles in determining cell identity in the inner ear. Specifically, our analysis revealed the role of the Zeb1/miR-200b pathway in establishing epithelial and mesenchymal identity in the inner ear. Furthermore, we detected a misregulation of the ZEB1 pathway in the inner ear of Twirler mice, which manifest, among other phenotypes, malformations of the auditory and vestibular labyrinth. The association of misregulation of the ZEB1/miR-200b pathway with auditory and vestibular defects in the Twirler mutant mice uncovers a novel mechanism underlying deafness and balance disorders. Our approach can be employed to decipher additional complex regulatory networks underlying other hearing and balance mouse mutants.

摘要

细胞异质性阻碍了从复杂哺乳动物器官的大规模表达谱中提取功能显著结果和推断调控网络。哺乳动物内耳由听觉和前庭系统组成,每个系统都由毛细胞、支持细胞、神经元、间充质细胞、其他上皮细胞和血管组成。我们开发了一种新的方案,可将新生小鼠内耳的听觉和前庭组织分类为其主要细胞成分。对分选细胞的转录组谱分析确定了细胞类型特异性表达簇。计算分析检测到在确定内耳细胞身份中起关键作用的转录因子和 microRNAs。具体来说,我们的分析揭示了 Zeb1/miR-200b 通路在建立内耳中上皮和间充质身份中的作用。此外,我们在内耳畸形的 Twirler 小鼠中检测到 ZEB1 通路的失调,其表现为听觉和前庭迷路的畸形等表型。Twirler 突变小鼠中 ZEB1/miR-200b 通路的失调与听觉和前庭缺陷的关联揭示了耳聋和平衡障碍的新机制。我们的方法可用于阐明其他听力和平衡小鼠突变体的其他复杂调控网络。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d5/3183091/f3d9d4f48960/pgen.1002309.g001.jpg

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