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A Critical E-box in Barhl1 3′ Enhancer Is Essential for Auditory Hair Cell Differentiation

机译:Barhl1 3增强子中的关键电子信箱对于听觉毛细胞分化至关重要

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摘要

Barhl1, a mouse homologous gene of Drosophila BarH class homeobox genes, is highly expressed within the inner ear and crucial for the long-term maintenance of auditory hair cells that mediate hearing and balance, yet little is known about the molecular events underlying Barhl1 regulation and function in hair cells. In this study, through data mining and in vitro report assay, we firstly identified Barhl1 as a direct target gene of Atoh1 and one E-box (E3) in Barhl1 3’ enhancer is crucial for Atoh1-mediated Barhl1 activation. Then we generated a mouse embryonic stem cell (mESC) line carrying disruptions on this E3 site E-box (CAGCTG) using CRISPR/Cas9 technology and this E3 mutated mESC line is further subjected to an efficient stepwise hair cell differentiation strategy in vitro. Disruptions on this E3 site caused dramatic loss of Barhl1 expression and significantly reduced the number of induced hair cell-like cells, while no affections on the differentiation toward early primitive ectoderm-like cells and otic progenitors. Finally, through RNA-seq profiling and gene ontology (GO) enrichment analysis, we found that this E3 box was indispensable for Barhl1 expression to maintain hair cell development and normal functions. We also compared the transcriptional profiles of induced cells from CDS mutated and E3 mutated mESCs, respectively, and got very consistent results except the Barhl1 transcript itself. These observations indicated that Atoh1-mediated Barhl1 expression could have important roles during auditory hair cell development. In brief, our findings delineate the detail molecular mechanism of Barhl1 expression regulation in auditory hair cell differentiation.
机译:Barhl1是果蝇BarH类同源盒基因的小鼠同源基因,在内耳内高表达,对于介导听力和平衡的听觉毛细胞的长期维持至关重要,但对Barhl1调控和调控的分子事件知之甚少。在毛细胞中起作用。在这项研究中,通过数据挖掘和体外报告分析,我们首先确定Barhl1是Atoh1的直接靶基因,而Barhl1 3’增强子中的一个E-box(E3)对于Atoh1介导的Barhl1激活至关重要。然后,我们使用CRISPR / Cas9技术在此E3位点E-box(CAGCTG)上产生了带有破坏的小鼠胚胎干细胞(mESC)系,并且对该E3突变的mESC系进一步进行了体外有效的逐步毛细胞分化策略。在这个E3位点的破坏导致Barhl1表达急剧下降,并显着减少了诱导的毛细胞样细胞的数量,而对早期原始外胚层样细胞和耳祖细胞的分化没有影响。最后,通过RNA序列分析和基因本体论(GO)富集分析,我们发现此E3框对于Barhl1表达维持毛细胞发育和正常功能是必不可少的。我们还比较了分别来自CDS突变和E3突变的mESC的诱导细胞的转录谱,除Barhl1转录本本身外,得到了非常一致的结果。这些观察结果表明Atoh1介导的Barhl1表达可能在听觉毛细胞发育过程中起重要作用。简而言之,我们的发现描述了在听觉毛细胞分化中Barhl1表达调节的详细分子机制。

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