The discovery, function, and regulation of epithelial splicing regulatory proteins (ESRP) 1 and 2

被引:4
|
作者
Derham, Jessica M. [1 ]
Kalsotra, Auinash [1 ,2 ,3 ]
机构
[1] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[2] Univ Illinois, Canc Ctr Illinois, Urbana, IL 61801 USA
[3] Univ Illinois, Carl R Woese Inst Genom Biol, Urbana, IL 61801 USA
关键词
MESENCHYMAL PLASTICITY; RECEPTOR SPECIFICITY; PANCREATIC-CANCER; FGFR2; LIMB; EXON; ISOFORM; HEPATOCYTES; TRANSITION; EXPRESSION;
D O I
10.1042/BST20221124
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alternative splicing is a broad and evolutionarily conserved mechanism to diversify gene expression and functionality. The process relies on RNA binding proteins (RBPs) to recognize and bind target sequences in pre-mRNAs, which allows for the inclusion or skipping of various alternative exons. One recently discovered family of RBPs is the epithelial splicing regulatory proteins (ESRP) 1 and 2. Here, we discuss the structure and physiological function of the ESRPs in a variety of contexts. We emphasize the current understanding of their splicing activities, using the classic example of fibroblast growth factor receptor 2 mutually exclusive splicing. We also describe the mechanistic roles of ESRPs in coordinating the splicing and functional output of key signaling pathways that support the maintenance of, or shift between, epithelial and mesenchymal cell states. In particular, we highlight their functions in the development of mammalian limbs, the inner ear, and craniofacial structure while discussing the genetic and biochemical evidence that showcases their conserved roles in tissue regeneration, disease, and cancer pathogenesis.
引用
收藏
页码:1097 / 1109
页数:13
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