The p53 gene with emphasis on its paralogues in mosquitoes

J Microbiol Immunol Infect. 2017 Dec;50(6):747-754. doi: 10.1016/j.jmii.2017.06.006. Epub 2017 Jun 29.

Abstract

The p53 gene is highly important in human cancers, as it serves as a tumor-suppressor gene. Subsequently, two p53 homologues, i.e., p73 and p63, with high identity of amino acids were identified, leading to construction of the p53 family. The p53 gene is highly important in human cancer because it usually transcribes genes that function by causing apoptosis in mammalian cells. In contrast, p63 and p73 tend to be more important in modulating development than inducing cell death, even though they share similar protein structures. Relatively recently, p53 was also identified in mosquitoes and many other insect species. Uniquely, its structure lacks the sterile alpha motif domain which is a putative protein-protein interaction domain and exclusively exists at the C-terminal region in p73 and p63 in mammals. A phylogenetic analysis revealed that the p53 gene derived from mosquitoes is composed of two paralogues, p53-1 and p53-2. Of these, only p53-2 is responsively upregulated by dengue 2 virus (DENV2) in C6/36 cells which usually survive the infection. This indicates that the p53 gene is closely related to DENV infection in mosquito cells. The specific significance of p53-2's involvement in cell survival from virus-induced stress is described and briefly discussed in this report.

Keywords: Cell survival; Mosquitoes; Paralogue; Phylogeny; p53 homologue.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis / genetics
  • Culicidae / genetics*
  • Dengue Virus / metabolism
  • Genes, p53 / genetics*
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Neoplasms / genetics
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Structure, Tertiary / genetics
  • Trans-Activators / genetics
  • Transcriptional Activation / genetics
  • Tumor Protein p73 / genetics
  • Tumor Protein p73 / metabolism*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation / genetics
  • Virus Replication / genetics

Substances

  • CKAP4 protein, human
  • Membrane Proteins
  • Protein Isoforms
  • TP73 protein, human
  • Trans-Activators
  • Tumor Protein p73
  • Tumor Suppressor Protein p53