神经元细胞类型特异性选择性剪接:一种指定大脑连接的机制?

Neurogenesis (Austin, Tex.) Pub Date : 2015-12-15 eCollection Date: 2015-01-01 DOI:10.1080/23262133.2015.1122699
Joshua Shing Shun Li, Grace Ji-Eun Shin, S Sean Millard
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引用次数: 4

摘要

选择性剪接(AS)允许单个基因产生多个蛋白质同种异构体。据推测,AS通过增加形成神经元之间连接所必需的细胞识别分子的数量,在大脑布线中发挥作用。许多研究已经描述了大脑中各种基因的异构体表达模式,但很少有研究表明特定的异构体是否在神经元布线中发挥功能作用。在我们最近的工作中,我们报道了细胞识别分子Dscam2的细胞类型特异性AS。Dscam2同种异构体的排他性表达允许紧密相关的神经元在相同的细胞类型中选择性地发出排斥信号,而不会相互干扰。我们发现,阻止2个密切相关神经元的细胞特异性异构体表达会破坏它们的轴突末端形态。我们提出对异构体特异性的要求延伸到突触,并讨论了可以直接测试这一点的实验。调节Dscam2细胞类型特异性AS的因子可能调节许多参与神经发育的基因剪接。这些选择性剪接的调节因子可以广泛地控制许多参与特定神经元类型发育的基因。识别这些因素是理解AS如何影响大脑连接组的关键一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain?

Neuronal cell-type-specific alternative splicing: A mechanism for specifying connections in the brain?

Alternative splicing (AS) allows a single gene to generate multiple protein isoforms. It has been hypothesized that AS plays a role in brain wiring by increasing the number of cell recognition molecules necessary for forming connections between neurons. Many studies have characterized isoform expression patterns of various genes in the brain, but very few have addressed whether specific isoforms play a functional role in neuronal wiring. In our recent work, we reported the cell-type-specific AS of the cell recognition molecule Dscam2. Exclusive expression of Dscam2 isoforms allows tightly associated neurons to signal repulsion selectively within the same cell-types, without interfering with one another. We show that preventing cell-specific isoform expression in 2 closely associated neurons disrupts their axon terminal morphology. We propose that the requirement for isoform specificity extends to synapses and discuss experiments that can test this directly. Factors that regulate Dscam2 cell-type-specific AS likely regulate the splicing of many genes involved in neurodevelopment. These regulators of alternative splicing may act broadly to control many genes involved in the development of specific neuron types. Identifying these factors is a key step in understanding how AS contributes to the brain connectome.

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