Promoter analysis and aberrant expression of the MUC5B gene in diffuse panbronchiolitis

被引:52
作者
Kamio, K
Matsushita, I
Hijikata, M
Kobashi, Y
Tanaka, G
Nakata, K
Ishida, T
Tokunaga, K
Taguchi, Y
Homma, S
Nakata, K
Azuma, A
Kudoh, S
Keicho, N
机构
[1] Int Med Ctr Japan, Dept Resp Dis, Inst Res, Shinjuku Ku, Tokyo 1628655, Japan
[2] Univ Tokyo, Grad Sch Sci, Dept Sci Biol, Unit Human Biol & Genet, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Human Genet, Tokyo, Japan
[4] Toho Univ, Sch Med, Dept Pulm Med, Tokyo 153, Japan
[5] Tenri Hosp, Dept Pathol, Nara, Japan
[6] Tenri Hosp, Dept Resp Med, Nara, Japan
关键词
case-control study; disease susceptibility; gene expression; immunohistochemistry; polymorphism;
D O I
10.1164/rccm.200409-1168OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Diffuse panbronchiolitis (DPB) is a chronic inflammatory airway disease predominantly affecting Asian populations. DPB is considered to be a complex genetic disease. Considering the mucous hypersecretion of the disease, we hypothesized that the transcriptional activity of mucin genes may be altered in DPB. We analyzed nucleotide sequences of regulatory region of six mucin genes-MUC1, MUC2, MUC4, MUC5AC, MUC5B, and MUC7-and detected their promoter polymorphisms. Among them, the insertion/deletion polymorphism identified in the MUC5B gene was significantly associated with the disease (p = 0.0001). Transcriptional activity observed in the three major promoter haplotypes corresponded to the strength of the disease association in which these haplotypes are involved. Immunohistochemistry of the lung tissues of DPB revealed that MUC5B was abundantly expressed not only in bronchial glands but also in increased numbers of goblet cells on the bronchial surface, where MUC5AC is predominant and MUC5B expression is generally scarce in the normal lung. Marked mucous hypersecretion observed in DPB may be partly explained by increased and aberrant expression of MUC58. The possible involvement of MUC5B gene in DPB was demonstrated. A further role of the MUC5B polymorphism in its pathogenesis should be studied in the future.
引用
收藏
页码:949 / 957
页数:9
相关论文
共 44 条
[1]   DELTA-F508 MUTATION OF CYSTIC-FIBROSIS GENE IS NOT FOUND IN CHRONIC-BRONCHITIS WITH SEVERE OBSTRUCTION IN JAPAN [J].
AKAI, S ;
OKAYAMA, H ;
SHIMURA, S ;
TANNO, Y ;
SASAKI, H ;
TAKISHIMA, T .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (03) :781-783
[2]   IL-4 and IL-13 up-regulate intestinal trefoil factor expression: Requirement for STAT6 and de novo protein synthesis [J].
Blanchard, C ;
Durual, S ;
Estienne, M ;
Bouzakri, K ;
Heim, MH ;
Blin, N ;
Cuber, JC .
JOURNAL OF IMMUNOLOGY, 2004, 172 (06) :3775-3783
[3]   Structure and chromosomal localization of the human salivary mucin gene, MUC7 [J].
Bobek, LA ;
Liu, JH ;
Sait, SNJ ;
Shows, TB ;
Bobek, YA ;
Levine, MJ .
GENOMICS, 1996, 31 (03) :277-282
[4]   Diffuse panbronchiolitis in an Asian immigrant [J].
Brugiere, O ;
Milleron, B ;
Antoine, M ;
Carette, MF ;
Philippe, C ;
Mayaud, C .
THORAX, 1996, 51 (10) :1065-1067
[5]   MUC1 gene polymorphism and gastric cancer - An epidemiological study [J].
Carvalho, F ;
Seruca, R ;
David, L ;
Amorim, A ;
Seixas, M ;
Bennett, E ;
Clausen, H ;
SobrinhoSimoes, M .
GLYCOCONJUGATE JOURNAL, 1997, 14 (01) :107-111
[6]   Characterization of human mucin 5B gene expression in airway epithelium and the genomic clone of the amino-terminal and 5′-flanking region [J].
Chen, Y ;
Zhao, YH ;
Di, YP ;
Wu, R .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 25 (05) :542-553
[7]  
Copin MC, 2000, INT J CANCER, V86, P162, DOI 10.1002/(SICI)1097-0215(20000415)86:2<162::AID-IJC3>3.0.CO
[8]  
2-R
[9]   Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene [J].
Emi, M ;
Keicho, N ;
Tokunaga, K ;
Katsumata, H ;
Souma, S ;
Nakata, K ;
Taguchi, Y ;
Ohishi, N ;
Azuma, A ;
Kudoh, S .
JOURNAL OF HUMAN GENETICS, 1999, 44 (03) :169-172
[10]  
Felsenstein J., 2005, PHYLIP PHYLOGENY INF, DOI DOI 10.1111/J.1096-0031.1989.TB00562.X