PR-Set7 is Degraded in a Conditional Cul4A Transgenic Mouse Model of Lung Cancer

Zhongguo Fei Ai Za Zhi. 2015 Jun;18(6):345-50. doi: 10.3779/j.issn.1009-3419.2015.06.15.

Abstract

Background: Maintenance of genomic integrity is essential to ensure normal organismal development and to prevent diseases such as cancer. PR-Set7 (also known as Set8) is a cell cycle regulated enzyme that catalyses monomethylation of histone 4 at Lys20 (H4K20me1) to promote chromosome condensation and prevent DNA damage. Recent studies show that CRL4CDT2-mediated ubiquitylation of PR-Set7 leads to its degradation during S phase and after DNA damage. This might occur to ensure appropriate changes in chromosome structure during the cell cycle or to preserve genome integrity after DNA damage.

Methods: We developed a new model of lung tumor development in mice harboring a conditionally expressed allele of Cul4A. We have therefore used a mouse model to demonstrate for the first time that Cul4A is oncogenic in vivo. With this model, staining of PR-Set7 in the preneoplastic and tumor lesions in AdenoCre-induced mouse lungs was performed. Meanwhile we identified higher protein level changes of γ-tubulin and pericentrin by IHC.

Results: The level of PR-Set7 down-regulated in the preneoplastic and adenocarcinomous lesions following over-expression of Cul4A. We also identified higher levels of the proteins pericentrin and γ-tubulin in Cul4A mouse lungs induced by AdenoCre.

Conclusions: PR-Set7 is a direct target of Cul4A for degradation and involved in the formation of lung tumors in the conditional Cul4A transgenic mouse model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle
  • Cullin Proteins / genetics
  • Cullin Proteins / metabolism*
  • Disease Models, Animal
  • Down-Regulation
  • Histone-Lysine N-Methyltransferase / genetics
  • Histone-Lysine N-Methyltransferase / metabolism*
  • Histones / metabolism
  • Humans
  • Lung / metabolism
  • Lung Neoplasms / genetics
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / physiopathology
  • Mice
  • Mice, Transgenic
  • Proteolysis
  • Tubulin / genetics
  • Tubulin / metabolism

Substances

  • CUL4A protein, human
  • Cullin Proteins
  • Histones
  • Tubulin
  • Histone-Lysine N-Methyltransferase
  • Setd8 protein, mouse