Karyopherin alpha2 is essential for rRNA transcription and protein synthesis in proliferative keratinocytes

PLoS One. 2013 Oct 3;8(10):e76416. doi: 10.1371/journal.pone.0076416. eCollection 2013.

Abstract

Karyopherin proteins mediate nucleocytoplasmic trafficking and are critical for protein and RNA subcellular localization. Recent studies suggest KPNA2 expression is induced in tumor cells and is strongly associated with prognosis, although the precise roles and mechanisms of KPNA2 overexpression in proliferative disorders have not been defined. We found that KPNA2 expression is induced in various proliferative disorders of the skin such as psoriasis, Bowen's disease, actinic keratosis, squamous cell carcinoma, Paget's disease, Merkel cell carcinoma, and mycosis fungoides. siRNA-mediated KPNA suppression revealed that KPNA2 is essential for significant suppression of HaCaT proliferation under starvation conditions. Ribosomal RNA transcription and protein synthesis were suppressed by starvation combined with knockdown of KPNA (including KPNA2) expression. KPNA2 localized to the nucleolus and interacted with proteins associated with mRNA processing, ribonucleoprotein complex biogenesis, chromatin modification, and transcription, as demonstrated by tandem affinity purification and mass spectrometry. KPNA2 may be an important promoter of ribosomal RNA and protein synthesis in tumor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Transformed
  • Cell Nucleus / metabolism
  • Cell Proliferation
  • Gene Expression
  • Gene Knockdown Techniques
  • Genes, rRNA*
  • Humans
  • Keratinocytes / metabolism*
  • Keratinocytes / pathology
  • Protein Binding
  • Protein Biosynthesis*
  • RNA Interference
  • Ribosomal Proteins / genetics
  • Ribosomal Proteins / metabolism
  • Skin / metabolism
  • Skin / pathology
  • Transcription, Genetic*
  • alpha Karyopherins / genetics
  • alpha Karyopherins / metabolism*

Substances

  • Ribosomal Proteins
  • alpha Karyopherins
  • karyopherin alpha 2

Grants and funding

This work was supported by a Grant-in-Aid of Scientific Research from the Ministry of Education, Culture, Science and Technology of Japan, and a Health and Labour Science Research Grant from the Ministry of Health, Labour and Welfare of Japan. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.