Fine mapping of the psoriasis susceptibility locus PSORS1 supports HLA-C as the susceptibility gene in the Han Chinese population

被引:75
作者
Fan, Xing [1 ,1 ]
Yang, Sen [1 ]
Huang, Wei [2 ]
Wang, Zhi-Min [2 ]
Sun, Liang-Dan [1 ]
Liang, Yan-Hua [1 ]
Gao, Min [1 ]
Ren, Yue-Qing [1 ]
Zhang, Kai-Yue [2 ]
Du, Wen-Hui [1 ]
Shen, Yu-Jun [1 ]
Liu, Jian-Jun [1 ,3 ]
Zhang, Xue-Jun [1 ]
机构
[1] Minist Educ, Key Lab Gene Resource Utilizat Genet Dis, Hefei, Anhui, Peoples R China
[2] Chinese Natl Human Genome Ctr Shanghai, Shanghai, Peoples R China
[3] Genome Inst Singapore, Singapore, Singapore
关键词
D O I
10.1371/journal.pgen.1000038
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
PSORS1 ( psoriasis susceptibility gene 1) is a major susceptibility locus for psoriasis. Several fine-mapping studies have highlighted a 300-kb candidate region of PSORS1 where multiple biologically plausible candidate genes were suggested. The most recent study has indicated HLA-Cw6 as the primary PSORS1 risk allele within the candidate region in a Caucasian population. In this study, a family-based association analysis of the PSORS1 locus was performed by analyzing 10 polymorphic microsatellite markers from the PSORS1 region as well as HLA- B, HLA- C and CDSN loci in 163 Chinese families of psoriasis. Five marker loci show strong evidence ( P, 10 23), and one marker locus shows weak evidence ( P = 0.04) for association. The haplotype cluster analysis showed that all the risk haplotypes are Cw6 positive and share a 369-kb region of homologous marker alleles which carries all the risk alleles, including HLA- Cw6 and CDSN*TTC, identified in this study. The recombinant haplotype analysis of the HLA- Cw6 and CDSN*TTC alleles in 228 Chinese families showed that the HLA- Cw6-/CDSN*TTC+ recombinant haplotype is clearly not associated with risk for psoriasis (T:NT = 29: 57, p = 0.0025) in a Chinese population, suggesting that the CDSN*TTC allele itself does not confer risk without the presence of the HLA- Cw6 allele. The further exclusion analysis of the non-risk HLA- Cw6 2/CDSN*TTC+ recombinant haplotypes with common recombination breakpoints has allowed us to refine the location of PSORS1 to a small candidate region. Finally, we performed a conditional linkage analysis and showed that the HLA- Cw6 is a major risk allele but does not explain the full linkage evidence of the PSORS1 locus in a Chinese population. By performing a series of family-based association analyses of haplotypes as well as an exclusion analysis of recombinant haplotypes, we were able to refine the PSORS1 gene to a small critical region where HLA-C is a strong candidate to be the PSORS1 susceptibility gene.
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相关论文
共 48 条
[1]   Merlin-rapid analysis of dense genetic maps using sparse gene flow trees [J].
Abecasis, GR ;
Cherny, SS ;
Cookson, WO ;
Cardon, LR .
NATURE GENETICS, 2002, 30 (01) :97-101
[2]   Corneodesmosin expression in psoriasis vulgaris differs from normal skin and other inflammatory skin disorders [J].
Allen, M ;
Ishida-Yamamoto, A ;
McGrath, J ;
Davison, S ;
Iizuka, H ;
Simon, M ;
Guerrin, M ;
Hayday, A ;
Vaughan, R ;
Serre, G ;
Trembath, R ;
Barker, J .
LABORATORY INVESTIGATION, 2001, 81 (07) :969-976
[3]   A non-HLA gene within the MHC in psoriasis [J].
Allen, MH ;
Veal, C ;
Faassen, A ;
Powis, SH ;
Vaughan, RW ;
Trembath, RC ;
Barker, JNWN .
LANCET, 1999, 353 (9164) :1589-1590
[4]   Corneodesmosin (CDSN) gene association with psoriasis vulgaris in Caucasian but not in Japanese populations [J].
Ameen, M ;
Allen, MH ;
Fisher, SA ;
Lewis, CM ;
Cuthbert, A ;
Kondeatis, E ;
Vaughan, RW ;
Murakami, H ;
Nakagawa, H ;
Barker, JNWN .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2005, 30 (04) :414-418
[5]   Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus [J].
Asumalahti, K ;
Veal, C ;
Laitinen, T ;
Suomela, S ;
Allen, M ;
Elomaa, O ;
Moser, M ;
de Cid, R ;
Ripatti, S ;
Vorechovsky, I ;
Marcusson, JA ;
Nakagawa, H ;
Lazaro, C ;
Estivill, X ;
Capon, F ;
Novelli, G ;
Saarialho-Kere, U ;
Barker, J ;
Trembath, R ;
Kere, J .
HUMAN MOLECULAR GENETICS, 2002, 11 (05) :589-597
[6]   A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele [J].
Asumalahti, K ;
Laitinen, T ;
Itkonen-Vatjus, R ;
Lokki, ML ;
Suomela, S ;
Snellman, E ;
Saarialho-Kere, U ;
Kere, J .
HUMAN MOLECULAR GENETICS, 2000, 9 (10) :1533-1542
[7]   Characterization of the major susceptibility region for psoriasis at chromosome 6p21.3 [J].
Balendran, N ;
Clough, RL ;
Arguello, JR ;
Barber, R ;
Veal, C ;
Jones, AB ;
Rosbotham, JL ;
Little, AM ;
Madrigal, A ;
Barker, JNWN ;
Powris, SH ;
Trembath, RC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (03) :322-328
[8]   Controlling the false discovery rate in behavior genetics research [J].
Benjamini, Y ;
Drai, D ;
Elmer, G ;
Kafkafi, N ;
Golani, I .
BEHAVIOURAL BRAIN RESEARCH, 2001, 125 (1-2) :279-284
[9]  
Bunce M., 1997, Tissue Antigens, V50, P100, DOI 10.1111/j.1399-0039.1997.tb02847.x
[10]  
Burden AD, 2000, BRIT J DERMATOL, V143, P238