The cytoskeleton and disease: Genetic disorders of intermediate filaments

被引:136
作者
Fuchs, E [1 ]
机构
[1] UNIV CHICAGO,DEPT MOL GENET & CELL BIOL,CHICAGO,IL 60637
关键词
intermediate filaments; cytoskeleton; protein structure; genetic disease; multigene family; protein function;
D O I
10.1146/annurev.genet.30.1.197
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Specialized cytoskeletons play many fascinating roles, including mechanical integrity and wound-healing in epidermal cells, cell polarity in simple epithelia, contraction in muscle cells, hearing and balance in the inner ear cells, axonal transport in neurons, and neuromuscular junction formation between muscle cells and motor neurons. These varied functions are dependent upon cytoplasmic networks of actin microfilaments (6 nm), intermediate filaments (10 nm) and microtubules (23 nm), and their many associated proteins. In this chapter, I review what is known about the cytoskeletons of intermediate filaments and their associated proteins. I focus largely on epidermal cells, which devote most of their protein-synthesizing machinery to producing an extensive intermediate filament network composed of keratin. Recent studies have shown that many of the devastating human disorders that arise from degeneration of this cell type have as their underlying basis either defects in the genes encoding keratins or abnormalities in keratin IF networks. I discuss what we know about the functions of IFs, and how the link to genetic disease hits enhanced this understanding.
引用
收藏
页码:197 / 231
页数:35
相关论文
共 184 条
[1]   THE FIBRILLAR SUBSTRUCTURE OF KERATIN FILAMENTS UNRAVELED [J].
AEBI, U ;
FOWLER, WE ;
REW, P ;
SUN, TT .
JOURNAL OF CELL BIOLOGY, 1983, 97 (04) :1131-1143
[2]   THE NUCLEAR LAMINA IS A MESHWORK OF INTERMEDIATE-TYPE FILAMENTS [J].
AEBI, U ;
COHN, J ;
BUHLE, L ;
GERACE, L .
NATURE, 1986, 323 (6088) :560-564
[3]   THE EXPRESSION OF MUTANT EPIDERMAL KERATIN CDNAS TRANSFECTED IN SIMPLE EPITHELIAL AND SQUAMOUS-CELL CARCINOMA LINES [J].
ALBERS, K ;
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1987, 105 (02) :791-806
[4]   EXPRESSION OF MUTANT KERATIN CDNAS IN EPITHELIAL-CELLS REVEALS POSSIBLE MECHANISMS FOR INITIATION AND ASSEMBLY OF INTERMEDIATE FILAMENTS [J].
ALBERS, K ;
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1989, 108 (04) :1477-1493
[5]   Mice expressing a mutant desmosomal cadherin exhibit abnormalities in desmosomes, proliferation, and epidermal differentiation [J].
Allen, E ;
Yu, QC ;
Fuchs, E .
JOURNAL OF CELL BIOLOGY, 1996, 133 (06) :1367-1382
[6]   ULTRASTRUCTURE OF INBORN-ERRORS OF KERATINIZATION .6. INHERITED ICHTHYOSES - MODEL SYSTEM FOR HETEROGENEITIES IN KERATINIZATION DISTURBANCES [J].
ANTONLAMPRECHT, I ;
SCHNYDER, UW .
ARCHIV FUR DERMATOLOGISCHE FORSCHUNG, 1974, 250 (03) :207-227
[8]   INTERMEDIATE FILAMENTS FORMED DENOVO FROM TAIL-LESS CYTOKERATINS IN THE CYTOPLASM AND IN THE NUCLEUS [J].
BADER, BL ;
MAGIN, TM ;
FREUDENMANN, M ;
STUMPP, S ;
FRANKE, WW .
JOURNAL OF CELL BIOLOGY, 1991, 115 (05) :1293-1307
[9]   COLORECTAL HYPERPLASIA AND INFLAMMATION IN KERATIN 8-DEFICIENT EVB/N MICE [J].
BARIBAULT, H ;
PENNER, J ;
IOZZO, RV ;
WILSONHEINER, M .
GENES & DEVELOPMENT, 1994, 8 (24) :2964-2973
[10]   MIDGESTATIONAL LETHALITY IN MICE LACKING KERATIN-8 [J].
BARIBAULT, H ;
PRICE, J ;
MIYAI, K ;
OSHIMA, RG .
GENES & DEVELOPMENT, 1993, 7 (7A) :1191-1202