PLoS ONE (Jan 2013)

Interaction between retinoid acid receptor-related orphan receptor alpha (RORA) and neuropeptide S receptor 1 (NPSR1) in asthma.

  • Nathalie Acevedo,
  • Annika Sääf,
  • Cilla Söderhäll,
  • Erik Melén,
  • Jami Mandelin,
  • Christina Orsmark Pietras,
  • Sini Ezer,
  • Piia Karisola,
  • Johanna Vendelin,
  • Gustav Boije af Gennäs,
  • Jari Yli-Kauhaluoma,
  • Harri Alenius,
  • Erika von Mutius,
  • Gert Doekes,
  • Charlotte Braun-Fahrländer,
  • Josef Riedler,
  • Marianne van Hage,
  • Mauro D'Amato,
  • Annika Scheynius,
  • Göran Pershagen,
  • Juha Kere,
  • Ville Pulkkinen

DOI
https://doi.org/10.1371/journal.pone.0060111
Journal volume & issue
Vol. 8, no. 4
p. e60111

Abstract

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Retinoid acid receptor-related Orphan Receptor Alpha (RORA) was recently identified as a susceptibility gene for asthma in a genome-wide association study. To investigate the impact of RORA on asthma susceptibility, we performed a genetic association study between RORA single nucleotide polymorphisms (SNPs) in the vicinity of the asthma-associated SNP (rs11071559) and asthma-related traits. Because the regulatory region of a previously implicated asthma susceptibility gene, Neuropeptide S receptor 1 (NPSR1), has predicted elements for RORA binding, we hypothesized that RORA may interact biologically and genetically with NPSR1. 37 RORA SNPs and eight NPSR1 SNPs were genotyped in the Swedish birth cohort BAMSE (2033 children) and the European cross-sectional PARSIFAL study (1120 children). Seven RORA SNPs confined into a 49 kb region were significantly associated with physician-diagnosed childhood asthma. The most significant association with rs7164773 (T/C) was driven by the CC genotype in asthma cases (OR = 2.0, 95%CI 1.36-2.93, p = 0.0003 in BAMSE; and 1.61, 1.18-2.19, p = 0.002 in the combined BAMSE-PARSIFAL datasets, respectively), and strikingly, the risk effect was dependent on the Gln344Arg mutation in NPSR1. In cell models, stimulation of NPSR1 activated a pathway including RORA and other circadian clock genes. Over-expression of RORA decreased NPSR1 promoter activity further suggesting a regulatory loop between these genes. In addition, Rora mRNA expression was lower in the lung tissue of Npsr1 deficient mice compared to wildtype littermates during the early hours of the light period. We conclude that RORA SNPs are associated with childhood asthma and show epistasis with NPSR1, and the interaction between RORA and NPSR1 may be of biological relevance. Combinations of common susceptibility alleles and less common functional polymorphisms may modify the joint risk effects on asthma susceptibility.