Genetic network identifies novel pathways contributing to atherosclerosis susceptibility in the innominate artery

BMC Med Genomics. 2014 Aug 12:7:51. doi: 10.1186/1755-8794-7-51.

Abstract

Background: Atherosclerosis, the underlying cause of cardiovascular disease, results from both genetic and environmental factors.

Methods: In the current study we take a systems-based approach using weighted gene co-expression analysis to identify a candidate pathway of genes related to atherosclerosis. Bioinformatic analyses are performed to identify candidate genes and interactions and several novel genes are characterized using in-vitro studies.

Results: We identify 1 coexpression module associated with innominate artery atherosclerosis that is also enriched for inflammatory and macrophage gene signatures. Using a series of bioinformatics analysis, we further prioritize the genes in this pathway and identify Cd44 as a critical mediator of the atherosclerosis. We validate our predictions generated by the network analysis using Cd44 knockout mice.

Conclusion: These results indicate that alterations in Cd44 expression mediate inflammation through a complex transcriptional network involving a number of previously uncharacterized genes.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Atherosclerosis / genetics*
  • Brachiocephalic Trunk / metabolism*
  • Computational Biology*
  • Gene Expression Regulation
  • Gene Regulatory Networks*
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Inflammation / genetics
  • Macrophages / metabolism
  • Mice
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Species Specificity
  • Transcription, Genetic

Substances

  • RNA, Messenger