Literature DB >> 14668478

Epidermolysis bullosa simplex-type mutations alter the dynamics of the keratin cytoskeleton and reveal a contribution of actin to the transport of keratin subunits.

Nicola Susann Werner1, Reinhard Windoffer, Pavel Strnad, Christine Grund, Rudolf Eberhard Leube, Thomas Michael Magin.   

Abstract

Dominant keratin mutations cause epidermolysis bullosa simplex by transforming keratin (K) filaments into aggregates. As a first step toward understanding the properties of mutant keratins in vivo, we stably transfected epithelial cells with an enhanced yellow fluorescent protein-tagged K14R125C mutant. K14R125C became localized as aggregates in the cell periphery and incorporated into perinuclear keratin filaments. Unexpectedly, keratin aggregates were in dynamic equilibrium with soluble subunits at a half-life time of <15 min, whereas filaments were extremely static. Therefore, this dominant-negative mutation acts by altering cytoskeletal dynamics and solubility. Unlike previously postulated, the dominance of mutations is limited and strictly depends on the ratio of mutant to wild-type protein. In support, K14R125C-specific RNA interference experiments resulted in a rapid disintegration of aggregates and restored normal filaments. Most importantly, live cell inhibitor studies revealed that the granules are transported from the cell periphery inwards in an actin-, but not microtubule-based manner. The peripheral granule zone may define a region in which keratin precursors are incorporated into existing filaments. Collectively, our data have uncovered the transient nature of keratin aggregates in cells and offer a rationale for the treatment of epidermolysis bullosa simplex by using short interfering RNAs.

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Year:  2003        PMID: 14668478      PMCID: PMC363056          DOI: 10.1091/mbc.e03-09-0687

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  54 in total

1.  Identification of the hemidesmosomal 500 kDa protein (HD1) as plectin.

Authors:  M Okumura; J Uematsu; Y Hirako; Y Nishizawa; H Shimizu; N Kido; K Owaribe
Journal:  J Biochem       Date:  1999-12       Impact factor: 3.387

2.  Disease severity correlates with position of keratin point mutations in patients with epidermolysis bullosa simplex.

Authors:  A Letai; P A Coulombe; M B McCormick; Q C Yu; E Hutton; E Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

Review 3.  Intermediate filaments: structure, dynamics, function, and disease.

Authors:  E Fuchs; K Weber
Journal:  Annu Rev Biochem       Date:  1994       Impact factor: 23.643

4.  Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses.

Authors:  P A Coulombe; M E Hutton; A Letai; A Hebert; A S Paller; E Fuchs
Journal:  Cell       Date:  1991-09-20       Impact factor: 41.582

5.  Targeted deletion of keratins 18 and 19 leads to trophoblast fragility and early embryonic lethality.

Authors:  M Hesse; T Franz; Y Tamai; M M Taketo; T M Magin
Journal:  EMBO J       Date:  2000-10-02       Impact factor: 11.598

6.  Detection of cytokeratin dynamics by time-lapse fluorescence microscopy in living cells.

Authors:  R Windoffer; R E Leube
Journal:  J Cell Sci       Date:  1999-12       Impact factor: 5.285

7.  A significant soluble keratin fraction in 'simple' epithelial cells. Lack of an apparent phosphorylation and glycosylation role in keratin solubility.

Authors:  C F Chou; C L Riopel; L S Rott; M B Omary
Journal:  J Cell Sci       Date:  1993-06       Impact factor: 5.285

Review 8.  Intermediate filaments on the move.

Authors:  Y H Chou; R D Goldman
Journal:  J Cell Biol       Date:  2000-08-07       Impact factor: 10.539

9.  A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseases.

Authors:  P A Coulombe; M E Hutton; R Vassar; E Fuchs
Journal:  J Cell Biol       Date:  1991-12       Impact factor: 10.539

10.  A nontetrameric species is the major soluble form of keratin in Xenopus oocytes and rabbit reticulocyte lysates.

Authors:  J B Bachant; M W Klymkowsky
Journal:  J Cell Biol       Date:  1996-01       Impact factor: 10.539

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  35 in total

1.  Identification of novel principles of keratin filament network turnover in living cells.

Authors:  Reinhard Windoffer; Stefan Wöll; Pavel Strnad; Rudolf E Leube
Journal:  Mol Biol Cell       Date:  2004-03-05       Impact factor: 4.138

2.  "Panta rhei": Perpetual cycling of the keratin cytoskeleton.

Authors:  Rudolf E Leube; Marcin Moch; Anne Kölsch; Reinhard Windoffer
Journal:  Bioarchitecture       Date:  2011-01

3.  Distinct Impact of Two Keratin Mutations Causing Epidermolysis Bullosa Simplex on Keratinocyte Adhesion and Stiffness.

Authors:  Melanie Homberg; Lena Ramms; Nicole Schwarz; Georg Dreissen; Rudolf E Leube; Rudolf Merkel; Bernd Hoffmann; Thomas M Magin
Journal:  J Invest Dermatol       Date:  2015-05-11       Impact factor: 8.551

Review 4.  Progress towards genetic and pharmacological therapies for keratin genodermatoses: current perspective and future promise.

Authors:  Jean Christopher Chamcheu; Gary S Wood; Imtiaz A Siddiqui; Deeba N Syed; Vaqar M Adhami; Joyce M Teng; Hasan Mukhtar
Journal:  Exp Dermatol       Date:  2012-07       Impact factor: 3.960

5.  E1--E4-mediated keratin phosphorylation and ubiquitylation: a mechanism for keratin depletion in HPV16-infected epithelium.

Authors:  Pauline B McIntosh; Peter Laskey; Kate Sullivan; Clare Davy; Qian Wang; Deborah J Jackson; Heather M Griffin; John Doorbar
Journal:  J Cell Sci       Date:  2010-07-27       Impact factor: 5.285

6.  Complementary roles of specific cysteines in keratin 14 toward the assembly, organization, and dynamics of intermediate filaments in skin keratinocytes.

Authors:  Xia Feng; Pierre A Coulombe
Journal:  J Biol Chem       Date:  2015-07-27       Impact factor: 5.157

7.  Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.

Authors:  Regina C Betz; Laura Planko; Sibylle Eigelshoven; Sandra Hanneken; Sandra M Pasternack; Heinrich Bussow; Kris Van Den Bogaert; Joerg Wenzel; Markus Braun-Falco; Arno Rutten; Michael A Rogers; Thomas Ruzicka; Markus M Nöthen; Thomas M Magin; Roland Kruse
Journal:  Am J Hum Genet       Date:  2006-01-19       Impact factor: 11.025

Review 8.  Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility.

Authors:  Pierre A Coulombe; Michelle L Kerns; Elaine Fuchs
Journal:  J Clin Invest       Date:  2009-07-01       Impact factor: 14.808

Review 9.  Types I and II Keratin Intermediate Filaments.

Authors:  Justin T Jacob; Pierre A Coulombe; Raymond Kwan; M Bishr Omary
Journal:  Cold Spring Harb Perspect Biol       Date:  2018-04-02       Impact factor: 10.005

Review 10.  The molecular basis of human keratin disorders.

Authors:  Meral Julia Arin
Journal:  Hum Genet       Date:  2009-02-27       Impact factor: 4.132

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