Emerging functions of SRSF1, splicing factor and oncoprotein, in RNA metabolism and cancer

• Published in: Molecular cancer research Vol. 12; no. 9; pp. 1195 - 1204
• Main Authors: Das, Shipra, Krainer, Adrian R
• Format: Journal Article
• Language: English
• Published: United States 01-09-2014
• Subjects: Cell Proliferation; Gene Expression Regulation, Neoplastic; Humans; Molecular Targeted Therapy; Neoplasms - genetics; Neoplasms - pathology; Nuclear Proteins - biosynthesis; Nuclear Proteins - genetics; Oncogene Proteins - biosynthesis; Oncogene Proteins - genetics; Proto-Oncogene Mas; RNA - genetics; RNA - metabolism; RNA Splicing - genetics; RNA, Messenger; RNA-Binding Proteins - biosynthesis; RNA-Binding Proteins - genetics; Serine-Arginine Splicing Factors
• ISSN: 1541-7786; 1557-3125
• DOI: 10.1158/1541-7786.mcr-14-0131

Serine/Arginine Splicing Factor 1 (SRSF1) is the archetype member of the SR protein family of splicing regulators. Since its discovery over two decades ago, SRSF1 has been repeatedly surprising and intriguing investigators by the plethora of complex biologic pathways it regulates. These include several key aspects of mRNA metabolism, such as mRNA splicing, stability, and translation, as well as other mRNA-independent processes, such as miRNA processing, protein sumoylation, and the nucleolar stress response. In this review, the structural features of SRSF1 are discussed as they relate to the intricate mechanism of splicing and the multiplicity of functions it performs. Similarly, a list of relevant alternatively spliced transcripts and SRSF1 interacting proteins is provided. Finally, emphasis is given to the deleterious consequences of overexpression of the SRSF1 proto-oncogene in human cancers, and the complex mechanisms and pathways underlying SRSF1-mediated transformation. The accumulated knowledge about SRSF1 provides critical insight into the integral role it plays in maintaining cellular homeostasis and suggests new targets for anticancer therapy. Mol Cancer Res; 12(9); 1195-204. ©2014 AACR.