Shaping human brain development and vulnerability through alternative splicing.

IF 11.1 Q1 CELL BIOLOGY Cell genomics Pub Date : 2024-06-12 DOI:10.1016/j.xgen.2024.100584
Francisco Aya, Juan Valcárcel
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引用次数: 0

Abstract

Alternative splicing contributes to shaping lineage-specific gene expression and phenotypes. In this issue of Cell Genomics, Recinos, Bao, Wang, et al.1 report that the balance between splicing isoforms of the microtubule-associated protein Tau in the brain is differentially regulated among primates by the RNA-binding protein MBNL2, with consequences for protein aggregation and neurodegeneration in humans.

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通过替代剪接塑造人类大脑的发育和脆弱性。
替代剪接有助于形成特定品系的基因表达和表型。在本期《细胞基因组学》(Cell Genomics)杂志上,Recinos、Bao、Wang 等人1 报告说,大脑中微管相关蛋白 Tau 的剪接异构体之间的平衡在灵长类动物中受到 RNA 结合蛋白 MBNL2 的不同调控,从而对人类的蛋白聚集和神经退行性变产生影响。
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