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首页> 外文期刊>The Journal of biological chemistry >The Musashi proteins MSI1 and MSI2 are required for photoreceptor morphogenesis and vision in mice
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The Musashi proteins MSI1 and MSI2 are required for photoreceptor morphogenesis and vision in mice

机译:Musashi蛋白MSI1和MSI2是小鼠的光感受器形态发生和视觉所必需的

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The Musashi family of RNA-binding proteins is known for its role in stem-cell renewal and is a negative regulator of cell differentiation. Interestingly, in the retina, the Musashi proteins MSI1 and MSI2 are differentially expressed throughout the cycle of retinal development, with MSI2 protein displaying robust expression in the adult retinal tissue. In this study, we investigated the importance of Musashi proteins in the development and function of photoreceptor neurons in the retina. We generated a pan-retinal and rod photoreceptor neuron-specific conditional KO mouse lacking MSI1 and MSI2. Independent of the sex, photoreceptor neurons with simultaneous deletion of Msi1 and Msi2 were unable to respond to light and displayed severely disrupted photoreceptor outer segment morphology and ciliary defects. Mice lacking MSI1 and MSI2 in the retina exhibited neuronal degeneration, with complete loss of photoreceptors within 6?months. In concordance with our earlier studies that proposed a role for Musashi proteins in regulating alternative splicing, the loss of MSI1 and MSI2 prevented the use of photoreceptor-specific exons in transcripts critical for outer segment morphogenesis, ciliogenesis, and synaptic transmission. Overall, we demonstrate a critical role for Musashi proteins in the morphogenesis of terminally differentiated photoreceptor neurons. This role is in stark contrast with the canonical function of these two proteins in the maintenance and renewal of stem cells.
机译:RNA结合蛋白的usashi系列以其在干细胞更新中的作用,是细胞分化的负调节因子。有趣的是,在视网膜中,Musashi蛋白MSI1和MSI2在整个视网膜发育循环中差异表达,MSI2蛋白显示成年视网膜组织中的稳健表达。在这项研究中,我们研究了usashi蛋白在视网膜中感光性神经元的发育和功能的重要性。我们产生了缺陷的泛视网膜和杆光感受器神经元特异性条件KO小鼠缺乏MSI1和MSI2。独立于性别,具有同时缺失MSI1和MSI2的光感受器神经元不能响应光并显示出严重破坏的感光体外部段形态和睫状缺损。视网膜中缺乏MSI1和MSI2的小鼠表现出神经元变性,在6?月内完全丧失光感受器。同时,与我们之前的研究提出了usashi蛋白在调节替代剪接中的作用,MSI1和MSI2的丧失阻止了在关键的转录物中使用感光体特异性外显子,对外部区段的形态发生,纤毛发生和突触传递。总体而言,我们证明了usashi蛋白在末端分化的光感受器神经元的形态发生中的关键作用。这种作用与在干细胞维持和更新中的这两种蛋白质的规范函数呈现。

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