QUANTITATIVE LOCUS ANALYSIS OF AIRWAY HYPERRESPONSIVENESS IN A/J AND C57BL/6J MICE

被引:228
作者
DESANCTIS, GT
MERCHANT, M
BEIER, DR
DREDGE, RD
GROBHOLZ, JK
MARTIN, TR
LANDER, ES
DRAZEN, JM
机构
[1] HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,COMBINED PROGRAM PULM & CRIT CARE MED,BOSTON,MA 02115
[2] WHITEHEAD INST BIOMED RES,MIT,CTR GENOME RES,CAMBRIDGE CTR,CAMBRIDGE,MA 02142
[3] HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DIV GENET,BOSTON,MA 02115
[4] CHILDRENS HOSP,DEPT PEDIAT,BOSTON,MA 02115
[5] MIT,DEPT BIOL,CAMBRIDGE,MA 02139
关键词
D O I
10.1038/ng1095-150
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Airway hyperresponsiveness is a key characteristic of human asthma and a marker for asthma-like conditions in animals. F-1 mice derived from A/J and C57BL/6J display a phenotype which resembles the asthma-like phenotype of the A/J mice. Since airway responsiveness failed to segregate as a mendelian trait, we show significant linkage at two loci, Bhr1 (lod = 3.0) and Bhr2 (lod = 3.7) on chromosomes 2 and 15. A third locus, Bhr3 (lod = 2.83), maps to chromosome 17. Each of these loci maps near candidate loci implicated in the pathobiology of asthma. Our study represents the first linkages established through a genome-wide survey of airway hyperresponsiveness in any mammal.
引用
收藏
页码:150 / 154
页数:5
相关论文
共 43 条
[1]   PLATELET-DERIVED GROWTH-FACTOR AND ITS RECEPTOR IN LUNGS FROM PATIENTS WITH ASTHMA AND CHRONIC AIR-FLOW OBSTRUCTION [J].
AUBERT, JD ;
HAYASHI, S ;
HARDS, J ;
BAI, TR ;
PARE, PD ;
HOGG, JC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :L655-L663
[2]   CYTOKINES AS MEDIATORS OF CHRONIC ASTHMA [J].
BARNES, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 150 (05) :S42-S49
[3]   CYTOKINES IN SYMPTOMATIC ASTHMA AIRWAYS [J].
BROIDE, DH ;
LOTZ, M ;
CUOMO, AJ ;
COBURN, DA ;
FEDERMAN, EC ;
WASSERMAN, SI .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (05) :958-967
[4]  
CAUGHEY GH, 1988, J PHARMACOL EXP THER, V244, P133
[5]  
CORRIGAN CJ, 1988, LANCET, V1, P1129
[6]   A GENETIC-MAP OF THE MOUSE WITH 4,006 SIMPLE SEQUENCE LENGTH POLYMORPHISMS [J].
DIETRICH, WF ;
MILLER, JC ;
STEEN, RG ;
MERCHANT, M ;
DAMRON, D ;
NAHF, R ;
GROSS, A ;
JOYCE, DC ;
WESSEL, M ;
DREDGE, RD ;
MARQUIS, A ;
STEIN, LD ;
GOODMAN, N ;
PAGE, DC ;
LANDER, ES .
NATURE GENETICS, 1994, 7 (02) :220-245
[7]   A ROLE FOR CELLULAR-IMMUNITY IN THE INDUCTION OF AIRWAY HYPERRESPONSIVENESS INDUCED BY SMALL MOLECULAR-WEIGHT COMPOUNDS [J].
GARSSEN, J ;
NIJKAMP, FP ;
VANDERVLIET, H ;
VANLOVEREN, H .
TOXICOLOGY LETTERS, 1994, 72 (1-3) :151-154
[8]   ELEVATED LUNG G-PROTEIN LEVELS AND MUSCARINIC RECEPTOR AFFINITY IN A MOUSE MODEL OF AIRWAY HYPERREACTIVITY [J].
GAVETT, SH ;
WILLSKARP, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (05) :L493-L500
[9]   MAST-CELLS AS A SOURCE OF MULTIFUNCTIONAL CYTOKINES [J].
GORDON, JR ;
BURD, PR ;
GALLI, SJ .
IMMUNOLOGY TODAY, 1990, 11 (12) :458-464
[10]  
HASHIMOTO S, 1993, ANN ALLERGY, V71, P455