Genetic disorders of the elastic fiber system

被引:122
作者
Milewicz, DM
Urbán, Z
Boyd, C
机构
[1] Univ Texas, Sch Med, Dept Internal Med, Houston, TX 77030 USA
[2] Univ Hawaii, Pacific Biomed Res Ctr, Honolulu, HI 96822 USA
关键词
supravalvular aortic stenosis; cutis laxa; Marfan syndrome; congenital contractual arachnodactyly; elastin; fibrillin;
D O I
10.1016/S0945-053X(00)00099-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the last decade, a considerable amount of new information has emerged describing the protein components of elastic fibers. It is now evident that elastic fibers are complex extracellular matrix polymers, composed of at least 19 different proteins that comprise both the microfibrillar and the amorphous components of elastic fibers. Mutations in three of the genes encoding the most abundant of these elastic fiber proteins result in a broad spectrum of elastic tissue phenotypes, ranging from skeletal and skin abnormalities to vascular and ocular defects. The following disorders will be discussed in this review: supravalvular aortic stenosis; Williams-Beuren syndrome; cutis laxa; Marfan syndrome; ectopia lentis; familial thoracic aortic aneurysms and dissections; MASS syndrome; isolated Skeletal features of Marfan syndrome; Shprintzen-Goldberg syndrome; and congenital contractural arachnodactyly. (C) 2000 Elsevier Science B.V. International Society of Matrix Biology. All rights reserved.
引用
收藏
页码:471 / 480
页数:10
相关论文
共 51 条
[1]   QUANTITATIVE DIFFERENCES IN BIOSYNTHESIS AND EXTRACELLULAR DEPOSITION OF FIBRILLIN IN CULTURED FIBROBLASTS DISTINGUISH 5 GROUPS OF MARFAN-SYNDROME PATIENTS AND SUGGEST DISTINCT PATHOGENETIC MECHANISMS [J].
AOYAMA, T ;
FRANCKE, U ;
DIETZ, HC ;
FURTHMAYR, H .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :130-137
[2]   A new mutation in the elastin gene causing supravalvular aortic stenosis [J].
Boeckel, T ;
Dierks, A ;
Vergopoulos, A ;
Bähring, S ;
Knoblauch, H ;
Müller-Myhsok, B ;
Baron, H ;
Aydin, A ;
Bein, G ;
Luft, FC ;
Schuster, H .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 83 (07) :1141-+
[3]   Functional domains on elastin and microfibril-associated glycoprotein involved in elastic fibre assembly [J].
BrownAugsburger, P ;
Broekelmann, T ;
Rosenbloom, J ;
Mecham, RP .
BIOCHEMICAL JOURNAL, 1996, 318 :149-155
[4]   A 2ND LOCUS FOR MARFAN-SYNDROME MAPS TO CHROMOSOME-3P24.2-P25 [J].
COLLOD, G ;
BABRON, MC ;
JONDEAU, G ;
COULON, M ;
WEISSENBACH, J ;
DUBOURG, O ;
BOURDARIAS, JP ;
BONAITIPELLIE, C ;
JUNIEN, C ;
BOILEAU, C .
NATURE GENETICS, 1994, 8 (03) :264-268
[5]   THE ELASTIN GENE IS DISRUPTED BY A TRANSLOCATION ASSOCIATED WITH SUPRAVALVULAR AORTIC-STENOSIS [J].
CURRAN, ME ;
ATKINSON, DL ;
EWART, AK ;
MORRIS, CA ;
LEPPERT, MF ;
KEATING, MT .
CELL, 1993, 73 (01) :159-168
[6]   MUTATIONS IN THE HUMAN GENE FOR FIBRILLIN-1 (FBN1) IN THE MARFAN-SYNDROME AND RELATED DISORDERS [J].
DIETZ, HC ;
PYERITZ, RE .
HUMAN MOLECULAR GENETICS, 1995, 4 :1799-1809
[7]   4 NOVEL FBN1 MUTATIONS - SIGNIFICANCE FOR MUTANT TRANSCRIPT LEVEL AND EGF-LIKE DOMAIN CALCIUM-BINDING IN THE PATHOGENESIS OF MARFAN-SYNDROME [J].
DIETZ, HC ;
MCINTOSH, I ;
SAKAI, LY ;
CORSON, GM ;
CHALBERG, SC ;
PYERITZ, RE ;
FRANCOMANO, CA .
GENOMICS, 1993, 17 (02) :468-475
[8]   FAMILIAL SUPRAVALVULAR AORTIC STENOSIS [J].
EISENBERG, R ;
YOUNG, D ;
JACOBSON, B ;
BOITO, A .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1964, 108 (04) :341-&
[9]   EXPRESSION OF A MUTANT HUMAN FIBRILLIN ALLELE UPON A NORMAL HUMAN OR MURINE GENETIC BACKGROUND RECAPITULATES A MARFAN CELLULAR PHENOTYPE [J].
ELDADAH, ZA ;
BRENN, T ;
FURTHMAYR, H ;
DIETZ, HC .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (02) :874-880
[10]   SUPRAVALVULAR AORTIC-STENOSIS ASSOCIATED WITH A DELETION DISRUPTING THE ELASTIN GENE [J].
EWART, AK ;
JIN, WS ;
ATKINSON, D ;
MORRIS, CA ;
KEATING, MT .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (03) :1071-1077