核心剪接结构和早期剪接体识别决定了微外显子对 SRRM3/4 的敏感性

Sophie Bonnal, Simon Bajew, Rosa Martinez Corral, Manuel Irimia
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引用次数: 0

摘要

微外显子对神经元和胰腺内分泌细胞的正常功能至关重要,在神经元和胰腺内分泌细胞中,微外显子的包含取决于剪接因子 SRRM3/4。然而,在胰腺细胞中,这些调节因子的较低表达限制了所有神经元微外显子中最敏感的子集的包含。虽然各种顺式作用元件都可能有助于微外显子的调控,但它们如何决定这种不同的剂量反应以及对 SRRM3/4 的高或低敏感性仍是未知数。在这里,对 28,535 个变体进行的大规模平行剪接分析表明,脊椎动物对 SRRM4 的敏感性是一致的,并支持一种调控模型,即微外显子敏感性的高低主要由核心剪接结构和长度限制之间的相互作用决定。在没有 SRRM3/4 的情况下,不同的剪接体活动以及假定两种微外显子仅在招募早期剪接体成分的效率上有所不同的数学模型进一步支持了这一结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Core splicing architecture and early spliceosomal recognition determine microexon sensitivity to SRRM3/4
Microexons are essential for proper functioning of neurons and pancreatic endocrine cells, where their inclusion depends on the splicing factors SRRM3/4. However, in pancreatic cells, lower expression of these regulators limits inclusion to only the most sensitive subset among all neuronal microexons. Although various cis-acting elements can contribute to microexon regulation, how they determine this differential dose response and high or low sensitivity to SRRM3/4 remains unknown. Here, Massively Parallel Splicing Assays probing 28,535 variants show that sensitivity to SRRM4 is conserved across vertebrates and support a regulatory model whereby high or low microexon sensitivity is largely determined by an interplay between core splicing architecture and length constraints. This conclusion is further supported by distinct spliceosome activities in the absence of SRRM3/4 and by a mathematical model that assumes that the two types of microexons differ only in their efficiency to recruit early spliceosomal components.
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