Structure and mapping of the human β-defensin HBD-2 gene and its expression at sites of inflammation

被引:223
作者
Liu, L
Wang, LN
Jia, HP
Zhao, CQ
Heng, HHQ
Schutte, BC
McCray, PB
Ganz, T
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Pathol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Will Rogers Inst Pulm Res, Los Angeles, CA 90095 USA
[4] Harbor UCLA Med Ctr, Dept Pathol, Los Angeles, CA USA
[5] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[6] York Univ, Dept Biol, N York, ON M3J 1P3, Canada
[7] SeeDNABiotech Inc, N York, ON M3J 1P3, Canada
关键词
host defense; epithelia; chromosome; 8p23; antimicrobial peptides;
D O I
10.1016/S0378-1119(98)00480-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We cloned a second human beta-defensin gene, HBD-2, and determined its gene structure and expression in inflamed tissue sections. The entire gene spanned about 2 kb with two small exons and one intron. Radiation hybrid studies confirmed the location on chromosome 8p, were consistent with the order HNP-1, HBD-1 and HBD-2, and located HBD-2 as the most centromeric of the genes. By three-color fluorescence in situ hybridization on both free chromatin fiber mapping and interphase mapping, HBD-1, HBD-2 and HNP-1 were mapped to chromosome 8p23. HBD-1 was within 40-100 kb of HNP-1, while HBD-2 was about 500-600 kb from HBD-1, with the most likely order HNP-1, HBD-1, HBD-2. The expression of HBD-2 was locally regulated by inflammation. HBD-2 mRNA was markedly increased in the epidermis surrounding inflamed regions, but not detectable in adjacent non-inflamed areas, a distribution that was confirmed at the peptide level by immunostaining with HBD-2 antibody. The HBD-2 gene is the first member of the human defensin family that is locally inducible by inflammation. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:237 / 244
页数:8
相关论文
共 21 条
[1]   HBD-1 - A NOVEL BETA-DEFENSIN FROM HUMAN PLASMA [J].
BENSCH, KW ;
RAIDA, M ;
MAGERT, HJ ;
SCHULZKNAPPE, P ;
FORSSMANN, WG .
FEBS LETTERS, 1995, 368 (02) :331-335
[2]  
BOMAN HG, 1995, ANNU REV IMMUNOL, V13, P61, DOI 10.1146/annurev.iy.13.040195.000425
[3]   RADIATION HYBRID MAPPING - A SOMATIC-CELL GENETIC METHOD FOR CONSTRUCTING HIGH-RESOLUTION MAPS OF MAMMALIAN CHROMOSOMES [J].
COX, DR ;
BURMEISTER, M ;
PRICE, ER ;
KIM, S ;
MYERS, RM .
SCIENCE, 1990, 250 (4978) :245-250
[4]   Inducible expression of an antibiotic peptide gene in lipopolysaccharide-challenged tracheal epithelial cells [J].
Diamond, G ;
Russell, JP ;
Bevins, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) :5156-5160
[5]   AIRWAY EPITHELIAL-CELLS ARE THE SITE OF EXPRESSION OF A MAMMALIAN ANTIMICROBIAL PEPTIDE GENE [J].
DIAMOND, G ;
JONES, DE ;
BEVINS, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (10) :4596-4600
[6]   The expression of the gene coding for the antibacterial peptide LL-37 is induced in human keratinocytes during inflammatory disorders [J].
Frohm, M ;
Agerberth, B ;
Ahangari, G ;
StahleBackdahl, M ;
Liden, S ;
Wigzell, H ;
Gudmundsson, GH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (24) :15258-15263
[7]  
Ganz T, 1997, SEMIN HEMATOL, V34, P343
[8]   A radiation hybrid map of the human genome [J].
Gyapay, G ;
Schmitt, K ;
Fizames, C ;
Jones, H ;
VegaCzarny, N ;
Spillett, D ;
Muselet, D ;
PrudHomme, JF ;
Dib, C ;
Auffray, C ;
Morissette, J ;
Weissenbach, J ;
Goodfellow, PN .
HUMAN MOLECULAR GENETICS, 1996, 5 (03) :339-346
[9]  
Hardaway R, 1997, INT J ENVIRON POLLUT, V7, P8
[10]   A peptide antibiotic from human skin [J].
Harder, J ;
Bartels, J ;
Christophers, E ;
Schroder, JM .
NATURE, 1997, 387 (6636) :861-861