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.
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Phagocytosis involves the engulfment and digestion of detrimental foreign objects (e.g., microbes) by different immune cells of our body, such as macrophages. Lipids play an important role during this immunological process, and hence, microbes have found ways to hijack these lipid pathways during phagocytosis to evade the immune system. For further information, see the review in this issue by Saharan and Kamat, pages 1279–1287. Image provided by Siddhesh Shashikant Kamat.
The discovery, function, and regulation of epithelial splicing regulatory proteins (ESRP) 1 and 2 Available to Purchase
Jessica M. Derham, Auinash Kalsotra; The discovery, function, and regulation of epithelial splicing regulatory proteins (ESRP) 1 and 2. Biochem Soc Trans 28 June 2023; 51 (3): 1097–1109. doi: https://doi.org/10.1042/BST20221124
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