SR蛋白
RNA剪接
剪接体
选择性拼接
丝氨酸
生物
RNA结合蛋白
细胞生物学
拼接因子
精氨酸
细胞质
外显子剪接增强剂
核糖核酸
生物化学
信使核糖核酸
基因
氨基酸
磷酸化
作者
Dianyang Li,Wenying Yu,Maode Lai
标识
DOI:10.1016/j.drudis.2023.103691
摘要
Serine- and arginine-rich splicing factors are pivotal modulators of constitutive splicing and alternative splicing that bind to the cis-acting elements in precursor mRNAs and facilitate the recruitment and assembly of the spliceosome. Meanwhile, SR proteins shuttle between the nucleus and cytoplasm with a broad implication in multiple RNA-metabolizing events. Recent studies have demonstrated the positive correlation of overexpression and/or hyperactivation of SR proteins and development of the tumorous phenotype, indicating the therapeutic potentials of targeting SR proteins. In this review, we highlight key findings concerning the physiological and pathological roles of SR proteins. We have also investigated small molecules and oligonucleotides that effectively modulate the functions of SR proteins, which could benefit future studies of SR proteins.
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