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Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways

机译:来自内耳感觉上皮细胞的小RNA的下一代测序可识别微RNA并定义调节途径

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Background The mammalian inner ear contains sensory organs, the organ of Corti in the cochlea and cristae and maculae in the vestibule, with each comprised of patterned sensory epithelia that are responsible for hearing and balance. The development, cell fate, patterning, and innervation of both the sensory and nonsensory regions of the inner ear are governed by tight regulation involving, among others, transcription factors and microRNAs (miRNAs). In humans, mutations in specific miRNA genes are associated with hearing loss. In mice, experimental reduction or mutations of miRNAs in the inner ear leads to severe developmental and structural abnormalities. A comprehensive identification of miRNAs in the sensory epithelia and their gene targets will enable pathways of auditory and vestibular function to be defined. Results In this study, we used Next-Generation Sequencing (NGS) to identify the most prominent miRNAs in the inner ear and to define miRNA-target pairs that form pathways crucial for the function of the sensory epithelial cells. NGS of RNA from inner ear sensory epithelial cells led to the identification of 455 miRNAs in both cochlear and vestibular sensory epithelium, with 30 and 44 miRNAs found in only cochlea or vestibule, respectively. miR-6715-3p and miR-6715-5p were defined for the first time in the inner ear. Gene targets were identified for each of these miRNAs, including Arhgap12, a GTPase activating protein, for miR-6715-3p, implicating this miRNA in sensory hair cell bundle development, actin reorganization, cell adhesion and inner ear morphogenesis. Conclusions This study provides a comprehensive atlas of miRNAs in the inner ear sensory epithelia. The results provide further support of the essential regulatory role of miRNAs in inner ear sensory epithelia and in regulating pathways that define development and growth of these cells.
机译:背景技术哺乳动物的内耳包含感觉器官,即耳蜗中的Corti器官以及前庭中的cr和黄斑,每个器官都由负责感觉和平衡的图案化感觉上皮组成。内耳的感觉和非感觉区域的发育,细胞命运,模式和神经支配都受到严格的调控,其中包括转录因子和微小RNA(miRNA)。在人类中,特定miRNA基因的突变与听力损失有关。在小鼠中,内耳中miRNA的实验性减少或突变会导致严重的发育和结构异常。感觉上皮细胞及其基因靶标中的miRNA的全面鉴定将使听觉和前庭功能的途径得以定义。结果在这项研究中,我们使用了下一代测序(NGS)来鉴定内耳中最突出的miRNA,并定义了形成对感觉上皮细胞功能至关重要的途径的miRNA-靶标对。来自内耳感觉上皮细胞的NGS RNA导致在耳蜗和前庭感觉上皮中鉴定到455个miRNA,仅在耳蜗或前庭中分别发现了30和44个miRNA。 miR-6715-3p和miR-6715-5p在内耳中首次定义。这些miRNA中的每一个均已确定了基因靶标,包括用于miR-6715-3p的GTPase活化蛋白Arhgap12,将这种miRNA牵涉到感觉性毛细胞束发育,肌动蛋白重组,细胞粘附和内耳形态发生。结论本研究提供了内耳感觉上皮细胞中miRNA的综合图集。结果为miRNA在内耳感觉上皮细胞以及定义这些细胞发育和生长的调控途径中的基本调控作用提供了进一步的支持。

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