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The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development.

机译:与眼球震颤相关的FRMD7基因调节神经元的生长和发育。

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摘要

Mutations in the gene encoding FERM domain-containing 7 protein (FRMD7) are recognized as an important cause of X-linked idiopathic infantile nystagmus (IIN). However, the precise role of FRMD7 and its involvement in the pathogenesis of IIN are not understood. In the present study, we have explored the role of FRMD7 in neuronal development. Using in situ hybridization and immunohistochemistry, we reveal that FRMD7 expression is spatially and temporally regulated in both the human and mouse brain during embryonic and fetal development. Furthermore, we show that FRMD7 expression is up-regulated upon retinoic acid (RA)-induced differentiation of mouse neuroblastoma NEURO2A cells, suggesting FRMD7 may play a role in this process. Indeed, we demonstrate, for the first time, that knockdown of FRMD7 during neuronal differentiation results in altered neurite development. Taken together, our data suggest that FRMD7 is involved in multiple aspects of neuronal development, and have direct importance to further understanding the pathogenesis of IIN.
机译:编码包含FERM域的7蛋白(FRMD7)的基因中的突变被认为是X连锁特发性婴儿眼球震颤(IIN)的重要原因。但是,FRMD7的确切作用及其在IIN发病机制中的作用尚不清楚。在本研究中,我们已经探索了FRMD7在神经元发育中的作用。使用原位杂交和免疫组织化学,我们揭示了FRMD7表达在胚胎和胎儿发育过程中在人和小鼠的大脑中时空调节。此外,我们显示在视黄酸(RA)诱导的小鼠神经母细胞瘤NEURO2A细胞分化后,FRMD7的表达上调,这表明FRMD7可能在此过程中起作用。确实,我们首次证明了在神经元分化过程中FRMD7的敲低导致神经突发育的改变。综上所述,我们的数据表明FRMD7参与神经元发育的多个方面,对进一步了解IIN的发病机理具有直接的重要性。

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