Protein-tyrosine phosphatase sigma is associated with ulcerative colitis

Curr Biol. 2007 Jul 17;17(14):1212-8. doi: 10.1016/j.cub.2007.06.013. Epub 2007 Jul 5.


Inflammatory bowel disease (IBD), a relatively common chronic debilitating intestinal illness, is composed of two broadly defined groups, Crohn's disease (CD) and ulcerative colitis (UC). Although several susceptibility genes for CD have been recently described, susceptibility genes exclusive for UC have not been forthcoming. Here, we show that receptor protein-tyrosine phosphatase sigma (PTPRS-encoding PTPsigma) knockout mice spontaneously develop mild colitis that becomes severe when challenged with two known inducers of colitis. We also demonstrate that E-cadherin and beta-catenin, two important adherens junction proteins involved in maintenance of barrier defense in the colon, act as colonic substrates for PTPsigma. Furthermore, we show that three SNPs (rs886936, rs17130, and rs8100586) that flank exon 8 in the human PTPRS gene are associated with UC. The presence of these SNPs is associated with novel splicing that removes the third immunoglobulin-like domain (exon 9) from the extracellular portion of PTPsigma, possibly altering dimerization or ligand recognition. We propose that polymorphisms in the human PTPRS gene lead to ulcerative colitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Animals
  • Biomarkers / metabolism
  • Cadherins / metabolism
  • Colitis, Ulcerative / enzymology*
  • Colitis, Ulcerative / genetics
  • Colitis, Ulcerative / metabolism
  • Colon / enzymology*
  • Colon / metabolism
  • Exons
  • Female
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Male
  • Mice
  • Mice, Knockout
  • Polymorphism, Single Nucleotide
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2 / genetics
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2 / metabolism*
  • beta Catenin / metabolism


  • Biomarkers
  • Cadherins
  • beta Catenin
  • Receptor-Like Protein Tyrosine Phosphatases, Class 2