Genome-wide analysis of the mouse LIM gene family reveals its roles in regulating pathological cardiac hypertrophy

FEBS Lett. 2021 Sep;595(17):2271-2289. doi: 10.1002/1873-3468.14168. Epub 2021 Aug 17.

Abstract

LIM-domain proteins have been shown to be associated with heart development and diseases. Systematic studies of LIM family members at the genome-wide level, which are crucial to further understand their functions in cardiac hypertrophy, are currently lacking. Here, 70 LIM genes were identified and characterised in mice. The expression patterns of LIM genes differ greatly during cardiac development and in the case of hypertrophy. Both Crip2 and Xirp2 are differentially expressed in cardiac hypertrophy and during heart failure. In addition, the hypertrophic state of cardiomyocytes is controlled by the relative expression levels of Crip2 and Xirp2. This study provides a foundation for further understanding of the special roles of LIM proteins in mammalian cardiac development and hypertrophy.

Keywords: LIM domain; cardiac development; cardiac hypertrophy; gene family; genomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiomegaly / genetics*
  • Cardiomegaly / pathology
  • Carrier Proteins / genetics
  • Cytoskeletal Proteins / genetics
  • Cytoskeleton / genetics
  • DNA-Binding Proteins / genetics
  • Electrocardiography
  • Gene Expression Regulation
  • Heart / embryology
  • Heart Failure / genetics
  • LIM Domain Proteins / genetics
  • LIM-Homeodomain Proteins / chemistry
  • LIM-Homeodomain Proteins / genetics*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Multigene Family
  • Phylogeny
  • Rats

Substances

  • Carrier Proteins
  • Crip2 protein, mouse
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • LIM Domain Proteins
  • LIM-Homeodomain Proteins
  • XIRP2 protein, mouse