Interleukin 9: A candidate gene for asthma

被引:187
作者
Nicolaides, NC
Holroyd, KJ
Ewart, SL
Eleff, SM
Kiser, MB
Dragwa, CR
Sullivan, CD
Grasso, L
Zhang, LY
Messler, CJ
Zhou, TY
Kleeberger, SR
Buetow, KH
Levitt, RC
机构
[1] MAGAININ PHARMACEUT, MAGAININ INST MOL MED, PLYMOUTH MEETING, PA 19462 USA
[2] MICHIGAN STATE UNIV, CTR VET MED, E LANSING, MI 48824 USA
[3] JOHNS HOPKINS MED INST, DEPT ANESTHESIOL & CRIT CARE MED, BALTIMORE, MD 21287 USA
[4] JOHNS HOPKINS MED INST, DEPT ENVIRONM HLTH SCI, BALTIMORE, MD 21287 USA
[5] FOX CHASE CANC CTR, DIV POPULAT SCI, PHILADELPHIA, PA 19111 USA
关键词
D O I
10.1073/pnas.94.24.13175
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Asthma is a complex heritable inflammatory disorder of the airways associated with clinical signs of atopy and bronchial hyperresponsiveness. Recent studies localized a major gene for asthma to chromosome 5q31-q33 in humans. Thus, this segment of the genome represents a candidate region for genes that determine susceptibility to bronchial hyperresponsiveness and atopy in animal models. Homologs of candidate genes on human chromosome 5q31-q33 are found in four regions in the mouse genome, two on chromosome 18, and one each on chromosomes 11 and 13. We assessed bronchial responsiveness as a quantitative trait in mice and found it linked to chromosome 13. Interleukin 9 (IL-9) is located in the linked region and was analyzed as a gene candidate. The expression of IL-9 was markedly reduced in bronchial hyporesponsive mice, and the level of expression was determined by sequences within the qualitative trait locus (QTL). These data suggest a role for IL-9 in the complex pathogenesis of bronchial hyperresponsiveness as a risk factor for asthma.
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页码:13175 / 13180
页数:6
相关论文
共 33 条
[21]  
Marsh DG, 1997, NAT GENET, V15, P389
[22]   ASTHMA [J].
MCFADDEN, ER ;
GILBERT, IA .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (27) :1928-1937
[23]   IL9 MAPS TO MOUSE CHROMOSOME-13 AND HUMAN CHROMOSOME-5 [J].
MOCK, BA ;
KRALL, M ;
KOZAK, CA ;
NESBITT, MN ;
MCBRIDE, OW ;
RENAULD, JC ;
VANSNICK, J .
IMMUNOGENETICS, 1990, 31 (04) :265-270
[24]   POSITIVE AUTOREGULATION OF C-MYB EXPRESSION VIA MYB BINDING-SITES IN THE 5' FLANKING REGION OF THE HUMAN C-MYB GENE [J].
NICOLAIDES, NC ;
GUALDI, R ;
CASADEVALL, C ;
MANZELLA, L ;
CALABRETTA, B .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :6166-6176
[25]   GENOMIC ORGANIZATION OF THE HUMAN PMS2 GENE FAMILY [J].
NICOLAIDES, NC ;
CARTER, KC ;
SHELL, BK ;
PAPADOPOULOS, N ;
VOGELSTEIN, B ;
KINZLER, KW .
GENOMICS, 1995, 30 (02) :195-206
[26]  
PAUWELS R, 1985, EUR J RESPIR DIS, V66, P98
[27]  
PETITFRERE C, 1993, IMMUNOLOGY, V79, P146
[28]   GENETIC SUSCEPTIBILITY TO ASTHMA - BRONCHIAL, HYPERRESPONSIVENESS COINHERITED WITH A MAJOR GENE FOR ATOPY [J].
POSTMA, DS ;
BLEECKER, ER ;
AMELUNG, PJ ;
HOLROYD, KJ ;
XU, JF ;
PANHUYSEN, CIM ;
MEYERS, DA ;
LEVITT, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (14) :894-900
[29]  
RENAULD JC, 1990, J IMMUNOL, V144, P4235
[30]   INTERLEUKIN-9 AND ITS RECEPTOR - INVOLVEMENT IN MAST-CELL DIFFERENTIATION AND T-CELL ONCOGENESIS [J].
RENAULD, JC ;
KERMOUNI, A ;
VINK, A ;
LOUAHED, J ;
VANSNICK, J .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 57 (03) :353-360