Literature DB >> 8982454

The cytoskeleton and disease: genetic disorders of intermediate filaments.

E Fuchs1.   

Abstract

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 has enhanced this understanding.

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Year:  1996        PMID: 8982454     DOI: 10.1146/annurev.genet.30.1.197

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  34 in total

1.  Identification with a recombinant antibody of an inner-ear cytokeratin, a marker for hair-cell differentiation.

Authors:  J L Cyr; A M Bell; A J Hudspeth
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

2.  Characterization of the chicken transitin gene reveals a strong relationship to the nestin intermediate filament class.

Authors:  A Napier; A Yuan; G J Cole
Journal:  J Mol Neurosci       Date:  1999-02       Impact factor: 3.444

3.  Modulation of cell proliferation by cytokeratins K10 and K16.

Authors:  J M Paramio; M L Casanova; C Segrelles; S Mittnacht; E B Lane; J L Jorcano
Journal:  Mol Cell Biol       Date:  1999-04       Impact factor: 4.272

Review 4.  Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disorders.

Authors:  N Gregersen; P Bross; M M Jørgensen; T J Corydon; B S Andresen
Journal:  J Inherit Metab Dis       Date:  2000-07       Impact factor: 4.982

Review 5.  The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders.

Authors:  N Gregersen; P Bross; B S Andrese; C B Pedersen; T J Corydon; L Bolund
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

6.  Acroplaxome, an F-actin-keratin-containing plate, anchors the acrosome to the nucleus during shaping of the spermatid head.

Authors:  Abraham L Kierszenbaum; Eugene Rivkin; Laura L Tres
Journal:  Mol Biol Cell       Date:  2003-08-07       Impact factor: 4.138

Review 7.  Softness, strength and self-repair in intermediate filament networks.

Authors:  Oliver I Wagner; Sebastian Rammensee; Neha Korde; Qi Wen; Jean-Francois Leterrier; Paul A Janmey
Journal:  Exp Cell Res       Date:  2007-04-27       Impact factor: 3.905

8.  The soft framework of the cellular machine.

Authors:  D A Weitz; P A Janmey
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-23       Impact factor: 11.205

9.  Disruption of NAD(P)H:quinone oxidoreductase 1 gene in mice leads to 20S proteasomal degradation of p63 resulting in thinning of epithelium and chemical-induced skin cancer.

Authors:  B A Patrick; X Gong; A K Jaiswal
Journal:  Oncogene       Date:  2010-11-01       Impact factor: 9.867

10.  Genetics of dark skin in mice.

Authors:  Karen R Fitch; Kelly A McGowan; Catherine D van Raamsdonk; Helmut Fuchs; Daekee Lee; Anne Puech; Yann Hérault; David W Threadgill; Martin Hrabé de Angelis; Gregory S Barsh
Journal:  Genes Dev       Date:  2003-01-15       Impact factor: 11.361

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