Physiological and Pathological Function of Serine/Arginine-Rich Splicing Factor 4 and Related Diseases

Biomed Res Int. 2018 Feb 12:2018:3819719. doi: 10.1155/2018/3819719. eCollection 2018.

Abstract

Serine/arginine-rich splicing factors (SRSFs) have one or two RNA recognition motifs in the N terminal and a serine/arginine-enriched domain in the C terminal. SRSFs are essential components of spliceosomes and are involved in alternative splicing, spliceosome assembly, mRNA export, and nonsense-mediated mRNA decay. The maintenance of cellular and tissue homeostasis relies on accurate alternative splicing, and various patterns of abnormal alternative splicing can cause different diseases. SRSF4 is associated with many physiological and pathological processes and has applications in the diagnosis and prognosis of specific diseases. In this review, we discuss knowledge of SRSF4 in physiological and pathological processes and highlight the applications of SRSF4 in the regulation of gene expression and associated diseases.

Publication types

  • Review

MeSH terms

  • Azoospermia / genetics
  • Azoospermia / metabolism
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Cell Line, Tumor
  • Female
  • Gene Expression Regulation / genetics
  • Humans
  • Hypertrophy, Left Ventricular / genetics
  • Hypertrophy, Left Ventricular / metabolism
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / metabolism
  • Male
  • Polymorphism, Single Nucleotide / genetics
  • Serine-Arginine Splicing Factors / genetics*
  • Serine-Arginine Splicing Factors / physiology*
  • Spliceosomes / genetics
  • Spliceosomes / physiology

Substances

  • SRSF4 protein, human
  • Serine-Arginine Splicing Factors