A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups - PubMed (original) (raw)
. 2004 Oct 15;13(20):2361-8.
doi: 10.1093/hmg/ddh273. Epub 2004 Aug 27.
Affiliations
- PMID: 15333584
- DOI: 10.1093/hmg/ddh273
A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups
Francesca Capon et al. Hum Mol Genet. 2004.
Abstract
Psoriasis is a chronic skin disorder with multifactorial aetiology. Genome-wide scans have provided unambiguous evidence for a major disease susceptibility locus on chromosome 6p21 (PSORS1). A minimal PSORS1 interval has been defined which encompasses three genes (HLA-C, HCR and CDSN) carrying psoriasis-associated SNPs. On the basis of this genetic evidence, we have undertaken an assessment of CDSN allele functional impact. A comparison of CDSN intragenic haplotypes showed that SNPs exclusive to disease-associated chromosomes are located in regions implicated in the stabilization of RNA transcripts. As CDSN is over-expressed in psoriatic lesions, we hypothesised that disease-associated intragenic SNPs may alter the rate of its mRNA decay. Here, we demonstrate that mRNAs transcribed from a CDSN risk haplotype present a 2-fold increase in stability, compared with those transcribed from a neutral haplotype (t-test P=0.004). Site-directed mutagenesis revealed that a single synonymous SNP (CDSN*971T) accounts for the observed increase in RNA stability. CDSN*971T maps to a RNA stability motif and UV cross-linking analysis demonstrated that the SNP affects the transcript affinity for a 39 kDa RNA binding protein. Association analyses show that haplotypes bearing CDSN*971T confer psoriasis susceptibility in a wide range of ethnic groups. These results demonstrate the effect of synonymous variation upon allele specific gene expression, a finding of relevance to future studies of the pathogenesis of common and complex traits.
Similar articles
- Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan.
Chang YT, Shiao YM, Chin PJ, Liu YL, Chou FC, Wu S, Lin YF, Li LH, Lin MW, Liu HN, Tsai SF. Chang YT, et al. Br J Dermatol. 2004 Jun;150(6):1104-11. doi: 10.1111/j.1365-2133.2004.05972.x. Br J Dermatol. 2004. PMID: 15214895 - Psoriasis vulgaris in Chinese individuals is associated with PSORS1C3 and CDSN genes.
Chang YT, Chou CT, Shiao YM, Lin MW, Yu CW, Chen CC, Huang CH, Lee DD, Liu HN, Wang WJ, Tsai SF. Chang YT, et al. Br J Dermatol. 2006 Oct;155(4):663-9. doi: 10.1111/j.1365-2133.2006.07420.x. Br J Dermatol. 2006. PMID: 16965413 - Psoriasis is associated with a SNP haplotype of the corneodesmosin gene (CDSN).
Orrù S, Giuressi E, Casula M, Loizedda A, Murru R, Mulargia M, Masala MV, Cerimele D, Zucca M, Aste N, Biggio P, Carcassi C, Contu L. Orrù S, et al. Tissue Antigens. 2002 Oct;60(4):292-8. doi: 10.1034/j.1399-0039.2002.600403.x. Tissue Antigens. 2002. PMID: 12472658 - Advances in the search for psoriasis susceptibility genes.
Capon F, Dallapiccola B, Novelli G. Capon F, et al. Mol Genet Metab. 2000 Sep-Oct;71(1-2):250-5. doi: 10.1006/mgme.2000.3031. Mol Genet Metab. 2000. PMID: 11001818 Review. - The genetic basis of psoriasis.
Valdimarsson H. Valdimarsson H. Clin Dermatol. 2007 Nov-Dec;25(6):563-7. doi: 10.1016/j.clindermatol.2007.08.010. Clin Dermatol. 2007. PMID: 18021893 Review.
Cited by
- Mechanistic role of a disease-associated genetic variant within the ADAM33 asthma susceptibility gene.
Del Mastro RG, Turenne L, Giese H, Keith TP, Van Eerdewegh P, May KJ, Little RD. Del Mastro RG, et al. BMC Med Genet. 2007 Jul 17;8:46. doi: 10.1186/1471-2350-8-46. BMC Med Genet. 2007. PMID: 17640346 Free PMC article. - Genome-wide approaches to schizophrenia.
Duan J, Sanders AR, Gejman PV. Duan J, et al. Brain Res Bull. 2010 Sep 30;83(3-4):93-102. doi: 10.1016/j.brainresbull.2010.04.009. Epub 2010 Apr 28. Brain Res Bull. 2010. PMID: 20433910 Free PMC article. Review. - Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk.
Karami S, Brennan P, Rosenberg PS, Navratilova M, Mates D, Zaridze D, Janout V, Kollarova H, Bencko V, Matveev V, Szeszenia-Dabrowska N, Holcatova I, Yeager M, Chanock S, Menashe I, Rothman N, Chow WH, Boffetta P, Moore LE. Karami S, et al. PLoS One. 2009 Sep 15;4(9):e7013. doi: 10.1371/journal.pone.0007013. PLoS One. 2009. PMID: 19753122 Free PMC article. - From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways.
Bauer-Mehren A, Furlong LI, Rautschka M, Sanz F. Bauer-Mehren A, et al. BMC Bioinformatics. 2009 Aug 27;10 Suppl 8(Suppl 8):S6. doi: 10.1186/1471-2105-10-S8-S6. BMC Bioinformatics. 2009. PMID: 19758470 Free PMC article. - A periodic pattern of mRNA secondary structure created by the genetic code.
Shabalina SA, Ogurtsov AY, Spiridonov NA. Shabalina SA, et al. Nucleic Acids Res. 2006 May 8;34(8):2428-37. doi: 10.1093/nar/gkl287. Print 2006. Nucleic Acids Res. 2006. PMID: 16682450 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials