Genetics of asthma and allergic disease

被引:121
作者
Cookson, WOC [1 ]
Moffatt, MF [1 ]
机构
[1] Wellcome Trust Ctr Human Genet Dis, Asthma Genet Grp, Oxford OX3 7BN, England
关键词
D O I
10.1093/hmg/9.16.2359
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atopic (allergic) asthma is the most common disease of childhood and is strongly genetic in origin. Many genome-wide screens for asthma and its associated traits have now been carried out, and genetic linkage has been consistently identified in several regions. It is probable that these loci contain major genes influencing atopy and asthma. Candidate genes have already been identified from the cytokine cluster on chromosome 5 and the MHC on chromosome 6. These complex regions contain more than one susceptibility locus for allergic disease. Other regions do not contain obvious candidate genes, and positional cloning of these loci is likely to identify novel disease pathways. Parent-of-origin effects are prominent at some of the loci and some also show linkage to other inflammatory immune diseases. Several single gene disorders are associated with allergic disease and on occasion are also linked to the same chromosomal regions. The positional cloning of asthma genes is now feasible.
引用
收藏
页码:2359 / 2364
页数:6
相关论文
共 109 条
[1]  
Akolkar PN, 1997, AM J GASTROENTEROL, V92, P2241
[2]   A polymorphism* in the 5′ flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E [J].
Baldini, M ;
Lohman, IC ;
Halonen, M ;
Erickson, RP ;
Holt, PG ;
Martinez, FD .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (05) :976-983
[3]  
Barnard J, 1999, J OBJECT-ORIENT PROG, V12, P12
[4]   Linkage of asthma and total serum IgE concentration to markers on chromosome 12q: Evidence from Afro-Caribbean and Caucasian populations [J].
Barnes, KC ;
Neely, JD ;
Duffy, DL ;
Freidhoff, LR ;
Breazeale, DR ;
Schou, C ;
Naidu, RP ;
Levett, PN ;
Renault, B ;
Kucherlapati, R ;
Iozzino, S ;
Ehrlich, E ;
Beaty, TH ;
Marsh, DG .
GENOMICS, 1996, 37 (01) :41-50
[5]   Human type 1 diabetes and the insulin gene: Principles of mapping polygenes [J].
Bennett, ST ;
Todd, JA .
ANNUAL REVIEW OF GENETICS, 1996, 30 :343-370
[6]  
Beyer K, 1998, J ALLERGY CLIN IMMUN, V101, pS152
[7]   Independent and epigenetic regulation of the interleukin-4 alleles in CD4+ T cells [J].
Bix, M ;
Locksley, RM .
SCIENCE, 1998, 281 (5381) :1352-1354
[8]   Prevalence of tumor necrosis factor-α and angiotensin converting enzyme polymorphisms in mild moderate and fatal/near-fatal asthma [J].
Chagani, T ;
Paré, PD ;
Zhu, S ;
Weir, TD ;
Bai, TR ;
Behbehani, NA ;
Fitzgerald, JM ;
Sandford, AJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (01) :278-282
[9]   Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping [J].
Chavanas, S ;
Garner, C ;
Bodemer, C ;
Ali, M ;
Hamel-Teillac, D ;
Wilkinson, J ;
Bonafé, JL ;
Paradisi, M ;
Kelsell, DP ;
Ansai, S ;
Mitsuhashi, Y ;
Larrègue, M ;
Leigh, IM ;
Harper, JI ;
Taïeb, A ;
de Prost, Y ;
Cardon, LR ;
Hovnanian, A .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (03) :914-921
[10]   Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome [J].
Chavanas, S ;
Bodemer, C ;
Rochat, A ;
Hamel-Teillac, D ;
Ali, M ;
Irvine, AD ;
Bonafé, JL ;
Wilkinson, J ;
Taïeb, A ;
Barrandon, Y ;
Harper, JI ;
de Prost, Y ;
Hovnanian, A .
NATURE GENETICS, 2000, 25 (02) :141-142