Literature DB >> 17122170

A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.

N Matsuzawa1, K Shimozato, N Natsume, N Niikawa, K Yoshiura.   

Abstract

Van der Woude syndrome (VWS) is an autosomal-dominant oral facial disorder. To find a gene mutation in a Japanese family using fingernail DNA samples, we performed this study. We hypothesized that a gene mutation in IRF6 might be involved in VWS, and that fingernail DNA samples may be valuable for detecting such mutations. Linkage and haplotype analyses of the family mapped the disease locus to the 1q32-q41 region. Mutation analysis with an improved extraction method for fingernail DNA detected a novel missense mutation (1046A>T, E349V) in exon 7 of IRF6 in all the affected members of the family. Since the E349V change may disturb the hydrophobic core and affect regulatory activity of IRF6, it is most likely that the mutation is causative for VWS in this family. Fingernail DNA is thus useful for linkage and mutation analyses, since the fingernail can be easily obtained non-invasively, sent through the mail, and stored for a long period. We emphasize here the usefulness of fingernail DNA for the genetic analysis of a disease.

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Year:  2006        PMID: 17122170     DOI: 10.1177/154405910608501215

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  3 in total

1.  Efficient DNA extraction from nail clippings using the protease solution from Cucumis melo.

Authors:  Shumi Yoshida-Yamamoto; Sayaka Nishimura; Teruko Okuno; Miki Rakuman; Yukio Takii
Journal:  Mol Biotechnol       Date:  2010-09       Impact factor: 2.695

2.  Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.

Authors:  Mitsuko Nakashima; Motoi Nakano; Akiyoshi Hirano; Tatsuya Kishino; Shinji Kondoh; Nobutomo Miwa; Norio Niikawa; Koh-Ichiro Yoshiura
Journal:  J Hum Genet       Date:  2007-11-07       Impact factor: 3.172

3.  Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.

Authors:  Renata L L Ferreira de Lima; Sarah A Hoper; Michella Ghassibe; Margaret E Cooper; Nicholas K Rorick; Shinji Kondo; Lori Katz; Mary L Marazita; John Compton; Sherri Bale; Ute Hehr; Michael J Dixon; Sandra Daack-Hirsch; Odile Boute; Bénédicte Bayet; Nicole Revencu; Christine Verellen-Dumoulin; Miikka Vikkula; Antônio Richieri-Costa; Danilo Moretti-Ferreira; Jeffrey C Murray; Brian C Schutte
Journal:  Genet Med       Date:  2009-04       Impact factor: 8.822

  3 in total

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