Literature DB >> 19157795

Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma.

Martha B Dua-Awereh1, Yutaka Shimomura, Liv Kraemer, Muhammad Wajid, Angela M Christiano.   

Abstract

BACKGROUND: Striate palmoplantar keratoderma (SPPK; OMIM #148700) is a rare autosomal dominant genodermatosis characterized by linear hyperkeratosis on the digits and hyperkeratosis on the palms and soles. SPPK is known to be caused by heterozygous mutations in either the desmoglein 1 (DSG1), desmoplakin (DSP), or keratin 1 (KRT1) genes.
OBJECTIVE: To define the molecular basis of SPPK in five Pakistani families showing a clear autosomal dominant inheritance pattern of SPPK.
METHODS: Based on previous reports of DSG1 mutations in SPPK, we performed direct sequencing of the DSG1 gene of all five families.
RESULTS: Mutation analysis resulted in the identification of one recurrent mutation (p.R26X) and four novel mutations (c.Ivs4-2A>G, c.515C>T, c.Ivs9-3C>G, and c.1399delA) in the DSG1 gene. Each mutation is predicted to cause haploinsufficiency of DSG1 protein.
CONCLUSION: The results of our study further underscore the significance of the desmoglein gene family in diseases of epidermal integrity.

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Year:  2009        PMID: 19157795      PMCID: PMC3986861          DOI: 10.1016/j.jdermsci.2008.11.005

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN: 0923-1811            Impact factor:   4.563


  20 in total

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Authors:  P A Frischmeyer; H C Dietz
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2.  Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratoderma.

Authors:  Neil V Whittock; Frances J Smith; Hong Wan; Rajeev Mallipeddi; W Andrew Griffiths; Patricia Dopping-Hepenstal; Gabrielle H Ashton; Robin A Eady; W H Irwin McLean; John A McGrath
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Review 3.  Getting under the skin of epidermal morphogenesis.

Authors:  Elaine Fuchs; Srikala Raghavan
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4.  Early death from cardiomyopathy in a family with autosomal dominant striate palmoplantar keratoderma and woolly hair associated with a novel insertion mutation in desmoplakin.

Authors:  Elizabeth E Norgett; Tom W Lucke; Bill Bowers; Colin S Munro; Irene M Leigh; David P Kelsell
Journal:  J Invest Dermatol       Date:  2006-04-20       Impact factor: 8.551

5.  The molecular architecture of cadherins in native epidermal desmosomes.

Authors:  Ashraf Al-Amoudi; Daniel Castaño Díez; Matthew J Betts; Achilleas S Frangakis
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6.  Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.

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7.  Defects in RNA splicing and the consequence of shortened translational reading frames.

Authors:  L E Maquat
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8.  Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma.

Authors:  D K Armstrong; K E McKenna; P E Purkis; K J Green; R A Eady; I M Leigh; A E Hughes
Journal:  Hum Mol Genet       Date:  1999-01       Impact factor: 6.150

9.  A nonsense mutation in the desmoglein 1 gene underlies striate keratoderma.

Authors:  Ana Kljuic; Leon Gilead; Amalia Martinez-Mir; Jorge Frank; Angela M Christiano; Abraham Zlotogorski
Journal:  Exp Dermatol       Date:  2003-08       Impact factor: 3.960

10.  Focal palmoplantar keratoderma caused by an autosomal dominant inherited mutation in the desmoglein 1 gene.

Authors:  M Milingou; P Wood; I Masouyé; W H McLean; L Borradori
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  7 in total

1.  Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families.

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Journal:  Hum Genet       Date:  2010-12-28       Impact factor: 4.132

Review 2.  Cadherins as targets for genetic diseases.

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Journal:  Cold Spring Harb Perspect Biol       Date:  2010-01       Impact factor: 10.005

3.  A spontaneous deletion within the desmoglein 3 extracellular domain of mice results in hypomorphic protein expression, immunodeficiency, and a wasting disease phenotype.

Authors:  Evgueni I Kountikov; Jonathan C Poe; Nancie J Maclver; Jeffrey C Rathmell; Thomas F Tedder
Journal:  Am J Pathol       Date:  2014-12-24       Impact factor: 4.307

4.  Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation.

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Review 5.  Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis.

Authors:  Natasha Caminsky; Eliseos J Mucaki; Peter K Rogan
Journal:  F1000Res       Date:  2014-11-18

6.  Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.

Authors:  M-L Lovgren; M A McAleer; A D Irvine; N J Wilson; S Tavadia; M E Schwartz; C Cole; A Sandilands; F J D Smith; M Zamiri
Journal:  Br J Dermatol       Date:  2017-04-02       Impact factor: 9.302

7.  Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families.

Authors:  Abida Akbar; Claire Prince; Chloe Payne; James Fasham; Wasim Ahmad; Emma L Baple; Andrew H Crosby; Gaurav V Harlalka; Asma Gul
Journal:  BMC Med Genet       Date:  2019-08-23       Impact factor: 2.103

  7 in total

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