Literature DB >> 17215264

Development of a DNA chip for the diagnosis of the most common corneal dystrophies caused by mutations in the betaigh3 gene.

So Young Yoo1, Tae-Im Kim, Sang Yup Lee, Eung Kweon Kim, Ki Chang Keum, Nae Choon Yoo, Won Min Yoo.   

Abstract

AIM: To develop a diagnostic DNA chip to detect mutations in the betaigh3 gene causing the most common corneal dystrophies (CDs).
METHODS: Samples from 98 people, including patients with betaigh3-associated CDs (beta-aCDs), were examined. Specific primer and probe sets were designed to examine exons 4 and 12 of the betaigh3 gene, in order to identify mutant and wild-type alleles. Mutations were then identified by hybridisation signals of sequence-specific probes immobilised on the slide glass.
RESULTS: Direct sequencing of exons 4 and 12 of the betaigh3 gene in the patients' genome showed that beta-aCDs could be mainly classified into five types: homozygotic Avellino corneal dystrophy (ACD), heterozygotic ACD, heterozygotic lattice CD I, heterozygotic Reis-Bucklers CD and heterozygotic granular CD. Blind tests were performed by applying the target DNA amplified from the genomic DNA isolated from the peripheral blood of the participants onto a DNA chip. The results obtained by DNA chip hybridisation matched well with the direct DNA sequencing results.
CONCLUSIONS: The DNA chip developed in this study allowed successful detection of beta-aCDs with a sensitivity of 100%. Mutational analysis of exons 4 and 12 of the betaigh3 gene, which are the mutational hot spots causing beta-aCDs, can be successfully performed with the DNA chip. Thus, this DNA chip-based method should allow a convenient, yet highly accurate, diagnosis of beta-aCDs, and can be further applied to diagnose other types of CDs.

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Year:  2007        PMID: 17215264      PMCID: PMC1955591          DOI: 10.1136/bjo.2006.111070

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  11 in total

1.  Corneal amyloidosis caused by Leu518Pro mutation of betaig-h3 gene.

Authors:  K Hirano; Y Hotta; K Fujiki; A Kanai
Journal:  Br J Ophthalmol       Date:  2000-06       Impact factor: 4.638

2.  Microarray-based identification of bacteria in clinical samples by solid-phase PCR amplification of 23S ribosomal DNA sequences.

Authors:  Georg Mitterer; Martin Huber; Ernst Leidinger; Claudia Kirisits; Werner Lubitz; Manfred W Mueller; Wolfgang M Schmidt
Journal:  J Clin Microbiol       Date:  2004-03       Impact factor: 5.948

3.  BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI.

Authors:  M F El-Ashry; M M Abd El-Aziz; L A Ficker; A J Hardcastle; S S Bhattacharya; N D Ebenezer
Journal:  Eye (Lond)       Date:  2004-07       Impact factor: 3.775

4.  Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.

Authors:  K Hirano; Y Hotta; M Nakamura; K Fujiki; A Kanai; N Yamamoto
Journal:  Cornea       Date:  2001-07       Impact factor: 2.651

5.  Varied appearance of cornea of patients with corneal dystrophy associated with R124H mutation in the BIGH3 gene.

Authors:  M Konishi; M Yamada; Y Nakamura; Y Mashima
Journal:  Cornea       Date:  1999-07       Impact factor: 2.651

6.  Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes.

Authors:  N A Afshari; J E Mullally; M A Afshari; R F Steinert; A P Adamis; D T Azar; J H Talamo; C H Dohlman; T P Dryja
Journal:  Arch Ophthalmol       Date:  2001-01

7.  Clinical outcome of eight BIGH3-linked corneal dystrophies.

Authors:  Pierre Ellies; Gilles Renard; Sophie Valleix; Pierre Yves Boelle; Paul Dighiero
Journal:  Ophthalmology       Date:  2002-04       Impact factor: 12.079

8.  Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.

Authors:  Anthony J Aldave; Julie G Gutmark; Vivek S Yellore; John A Affeldt; Mario A Meallet; Nitin Udar; Narsing A Rao; Kent W Small; Gordon K Klintworth
Journal:  Am J Ophthalmol       Date:  2004-11       Impact factor: 5.258

9.  H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people.

Authors:  H M Chau; N T Ha; L X Cung; T K Thanh; K Fujiki; A Murakami; A Kanai
Journal:  Br J Ophthalmol       Date:  2003-06       Impact factor: 4.638

10.  Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis.

Authors:  Shigeo Yoshida; Ayako Yoshida; Shintaro Nakao; Aki Emori; Takao Nakamura; Kimihiko Fujisawa; Yuji Kumano; Tatsuro Ishibashi
Journal:  Am J Ophthalmol       Date:  2004-03       Impact factor: 5.258

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  1 in total

1.  TGFBI Gene Mutation Analysis of Clinically Diagnosed Granular Corneal Dystrophy Patients Prior to PTK: A Pilot Study from Eastern China.

Authors:  Li Zeng; Jing Zhao; Yingjun Chen; Feng Zhao; Meiyan Li; Connie Chao-Shern; Tara Moore; John Marshall; Xingtao Zhou
Journal:  Sci Rep       Date:  2017-04-04       Impact factor: 4.379

  1 in total

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