Drosophila matrix metalloproteinases are required for tissue remodeling, but not embryonic development

被引:196
作者
Page-McCaw, A [1 ]
Serano, J [1 ]
Santé, JM [1 ]
Rubin, GM [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cellular Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
关键词
D O I
10.1016/S1534-5807(02)00400-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The matrix metalloproteinase (MMP) family is heavily implicated in many diseases, including cancer. The developmental functions of these genes are not clear, however, because the >20 mammalian MMPs can be functionally redundant. Drosophila melanogaster has only two MMPs, which are expressed in embryos in distinct patterns. We created mutations in both genes: Mmp1 mutants have defects in larval tracheal growth and pupal head eversion, and Mmp2 mutants have defects in larval tissue histolysis and epithelial fusion during metamorphosis; neither is required for embryonic development. Double mutants also complete embryogenesis, and these represent the first time, to our knowledge, that all MMPs have been disrupted in any organism. Thus, MMPs are not required for Drosophila embryonic development, but, rather, for tissue remodeling.
引用
收藏
页码:95 / 106
页数:12
相关论文
共 41 条
[1]   The genome sequence of Drosophila melanogaster [J].
Adams, MD ;
Celniker, SE ;
Holt, RA ;
Evans, CA ;
Gocayne, JD ;
Amanatides, PG ;
Scherer, SE ;
Li, PW ;
Hoskins, RA ;
Galle, RF ;
George, RA ;
Lewis, SE ;
Richards, S ;
Ashburner, M ;
Henderson, SN ;
Sutton, GG ;
Wortman, JR ;
Yandell, MD ;
Zhang, Q ;
Chen, LX ;
Brandon, RC ;
Rogers, YHC ;
Blazej, RG ;
Champe, M ;
Pfeiffer, BD ;
Wan, KH ;
Doyle, C ;
Baxter, EG ;
Helt, G ;
Nelson, CR ;
Miklos, GLG ;
Abril, JF ;
Agbayani, A ;
An, HJ ;
Andrews-Pfannkoch, C ;
Baldwin, D ;
Ballew, RM ;
Basu, A ;
Baxendale, J ;
Bayraktaroglu, L ;
Beasley, EM ;
Beeson, KY ;
Benos, PV ;
Berman, BP ;
Bhandari, D ;
Bolshakov, S ;
Borkova, D ;
Botchan, MR ;
Bouck, J ;
Brokstein, P .
SCIENCE, 2000, 287 (5461) :2185-2195
[2]  
Beitel GJ, 2000, DEVELOPMENT, V127, P3271
[3]   TGF-β3-induced palatogenesis requires matrix metalloproteinases [J].
Blavier, L ;
Lazaryev, A ;
Groffen, J ;
Heisterkamp, N ;
DeClerck, YA ;
Kaartinen, V .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (05) :1457-1466
[4]  
BRAND AH, 1993, DEVELOPMENT, V118, P401
[5]  
CHOU TB, 1993, DEVELOPMENT, V119, P1359
[6]  
Chou TB, 1996, GENETICS, V144, P1673
[7]  
Damjanovski S, 2000, ANN NY ACAD SCI, V926, P180
[8]   Targeted deletion of matrix metalloproteinase-9 attenuates left ventricular enlargement and collagen accumulation after experimental myocardial infarction [J].
Ducharme, A ;
Frantz, S ;
Aikawa, M ;
Rabkin, E ;
Lindsey, M ;
Rohde, LE ;
Schoen, FJ ;
Kelly, RA ;
Werb, Z ;
Libby, P ;
Lee, RT .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (01) :55-62
[9]   New functions for the matrix metalloproteinases in cancer progression [J].
Egeblad, M ;
Werb, Z .
NATURE REVIEWS CANCER, 2002, 2 (03) :161-174
[10]   Inflated wings, tissue autolysis and early death in tissue inhibitor of metalloproteinases mutants of Drosophila [J].
Godenschwege, TA ;
Pohar, N ;
Buchner, S ;
Buchner, E .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2000, 79 (07) :495-501