Small kinetochore associated protein (SKAP) promotes UV-induced cell apoptosis through negatively regulating pre-mRNA processing factor 19 (Prp19)

PLoS One. 2014 Apr 9;9(4):e92712. doi: 10.1371/journal.pone.0092712. eCollection 2014.

Abstract

Apoptosis is a regulated cellular suicide program that is critical for the development and maintenance of healthy tissues. Previous studies have shown that small kinetochore associated protein (SKAP) cooperates with kinetochore and mitotic spindle proteins to regulate mitosis. However, the role of SKAP in apoptosis has not been investigated. We have identified a new interaction involving SKAP, and we propose a mechanism through which SKAP regulates cell apoptosis. Our experiments demonstrate that both overexpression and knockdown of SKAP sensitize cells to UV-induced apoptosis. Further study has revealed that SKAP interacts with Pre-mRNA processing Factor 19 (Prp19). We find that UV-induced apoptosis can be inhibited by ectopic expression of Prp19, whereas silencing Prp19 has the opposite effect. Additionally, SKAP negatively regulates the protein levels of Prp19, whereas Prp19 does not alter SKAP expression. Finally, rescue experiments demonstrate that the pro-apoptotic role of SKAP is executed through Prp19. Taken together, these findings suggest that SKAP promotes UV-induced cell apoptosis by negatively regulating the anti-apoptotic protein Prp19.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Apoptosis / radiation effects*
  • Cell Cycle Proteins / chemistry
  • Cell Cycle Proteins / metabolism*
  • Cell Line
  • Chromatography, Affinity
  • Conserved Sequence
  • DNA Repair Enzymes / genetics*
  • DNA Repair Enzymes / metabolism
  • Evolution, Molecular
  • Gene Knockdown Techniques
  • Gene Silencing / radiation effects
  • Humans
  • Mass Spectrometry
  • Microtubule-Associated Proteins / chemistry
  • Microtubule-Associated Proteins / metabolism*
  • Molecular Sequence Data
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Protein Binding / radiation effects
  • RNA Splicing Factors
  • Ultraviolet Rays*

Substances

  • Cell Cycle Proteins
  • KNSTRN protein, human
  • Microtubule-Associated Proteins
  • Nuclear Proteins
  • RNA Splicing Factors
  • DNA Repair Enzymes
  • PRPF19 protein, human

Grants and funding

This work was supported by the State Key Laboratory Special fund from the Ministry of Science (2060204), grants from the National Important Research Plan of China (2012BAI31B08, 2012CB944902, and 2011CB944302), a grant from the National Natural Sciences Foundation of China (81101855), and grants from the Specialized Research Fund for the Doctoral Program of Higher Education (20111106120018, 20111106120018). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.