4.8 Article

A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

Journal

NATURE COMMUNICATIONS
Volume 7, Issue -, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/ncomms12342

Keywords

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Funding

  1. National Institute of Diabetes and Digestive and Kidney Disease (NIDDK) [DK064869, DK062432]
  2. National Human Genome Research Institute (NHGRI) [DK064869, DK043351, HG005923]
  3. Crohns and Colitis Foundation [3765]
  4. Leona M. AMP
  5. Harry B. Helmsley Charitable Trust [2015PG-IBD001]
  6. Amgen [2013583217]
  7. CCFA [3765]
  8. Cedars-Sinai F. Widjaja Foundation
  9. European Union [DK062413, AI067068, U54DE023789-01, 305479]
  10. Leona M. and Harry B. Helmsley Charitable Trust
  11. Crohn's and Colitis Foundation of America
  12. NIH [DK062431, U01 DK062429, U01 DK062422, R01 DK092235, U01 DK062420]
  13. Medical Research Council, UK [MR/J00314X/1]
  14. Wellcome Trust [WT091310, 098051]
  15. Inflammatory Bowel Disease Genetic Research Chair at the University of Pittsburgh
  16. [PO1DK046763]
  17. MRC [MC_UU_12010/7, G0800759, G0600329, MR/J00314X/1] Funding Source: UKRI
  18. Chief Scientist Office [ETM/137] Funding Source: researchfish
  19. Medical Research Council [MC_UU_12010/7, G0600329, G0800759, MR/J00314X/1] Funding Source: researchfish
  20. National Institute for Health Research [NIHR-RP-R3-12-026, ACF-2014-23-002] Funding Source: researchfish

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Protein-truncating variants protective against human disease provide in vivo validation of therapeutic targets. Here we used targeted sequencing to conduct a search for protein-truncating variants conferring protection against inflammatory bowel disease exploiting knowledge of common variants associated with the same disease. Through replication genotyping and imputation we found that a predicted protein-truncating variant (rs36095412, p.R179X, genotyped in 11,148 ulcerative colitis patients and 295,446 controls, MAF = up to 0.78%) in RNF186, a single-exon ring finger E3 ligase with strong colonic expression, protects against ulcerative colitis (overall P = 6.89 x 10(-7), odds ratio = 0.30). We further demonstrate that the truncated protein exhibits reduced expression and altered subcellular localization, suggesting the protective mechanism may reside in the loss of an interaction or function via mislocalization and/or loss of an essential transmembrane domain.

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