Guarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathway

Wiley Interdiscip Rev RNA. 2011 Jul-Aug;2(4):507-22. doi: 10.1002/wrna.73. Epub 2011 Jan 20.

Abstract

Ribosomes, the molecular factories that carry out protein synthesis, are essential for every living cell. Ribosome biogenesis, the process of ribosome synthesis, is highly complex and energy consuming. Over the last decade, many exciting and novel findings have linked various aspects of ribosome biogenesis to cell growth and cell cycle control. Defects in ribosome biogenesis have also been linked to human diseases. It is now clear that disruption of ribosome biogenesis causes nucleolar stress that triggers a p53 signaling pathway, thus providing cells with a surveillance mechanism for monitoring ribosomal integrity. Although the exact mechanisms of p53 induction in response to nucleolar stress are still unknown, several ribosomal proteins have been identified as key players in this ribosome-p53 signaling pathway. Recent studies of human ribosomal pathologies in a variety of animal models have also highlighted the role of this pathway in the pathophysiology of these diseases. However, it remains to be understood why the effect of ribosomal malfunction is not a universal response in all cell types but is restricted to particular tissues, causing the specific phenotypes seen in ribosomal diseases. A challenge for future studies will be to identify additional players in this signaling pathway and to elucidate the underlying molecular mechanisms that link defective ribosome synthesis to p53.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anemia, Diamond-Blackfan / genetics
  • Anemia, Diamond-Blackfan / metabolism
  • Anemia, Macrocytic / genetics
  • Anemia, Macrocytic / metabolism
  • Animals
  • Chromosome Deletion
  • Chromosomes, Human, Pair 5 / genetics
  • Chromosomes, Human, Pair 5 / metabolism
  • Dyskeratosis Congenita / genetics
  • Dyskeratosis Congenita / metabolism
  • Genes, p53
  • Humans
  • Mandibulofacial Dysostosis / genetics
  • Mandibulofacial Dysostosis / metabolism
  • Models, Biological
  • Protein Biosynthesis*
  • Ribosomal Proteins / biosynthesis
  • Ribosomal Proteins / deficiency
  • Ribosomal Proteins / genetics
  • Ribosomes / genetics*
  • Ribosomes / metabolism*
  • Signal Transduction
  • Stress, Physiological
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Ribosomal Proteins
  • Tumor Suppressor Protein p53

Supplementary concepts

  • Chromosome 5q Deletion Syndrome