Literature DB >> 15221638

Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients.

Tomomi Uyeda1, Toru Takahashi1, Shuji Eto1, Takumi Sato1, Gang Xu1, Rika Kanezaki1, Tsutomu Toki1, Susumu Yonesaka2, Etsuro Ito3.   

Abstract

Marfan syndrome (MFS) is an autosomal dominant disorder of the extracellular matrix. Allelic variations in the gene for fibrillin-1 ( FBN1) have been shown to cause MFS. To date, over 550 mutations have been identified in patients with MFS and related connective tissue diseases. However, about a half of MFS cases do not possess mutations in the FBN1 gene. These findings raise the possibility that variants located in other genes cause or modify MFS. To explore this possibility, firstly we analyzed FBN1 allelic variants in 12 Japanese patients with MFS, and secondly we analyzed fibrillin-3 gene ( FBN3) in patients without FBN1 mutations using conformation sensitive gel electrophoresis (CSGE) and direct sequencing analysis. We identified three novel FBN1 mutations and ten FBN3 single nucleotide polymorphisms (SNPs). In this report, we could not detect a responsible mutation of the FBN3 gene for MFS. Although the number of the cases in this report is small, at least these results suggest that disease-causing mutations in exon regions of the FBN3 gene are very rare in MFS.

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Year:  2004        PMID: 15221638     DOI: 10.1007/s10038-004-0168-x

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  11 in total

1.  Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2.

Authors:  Laurence Faivre; André Mégarbané; Abdulrahman Alswaid; Louise Zylberberg; Noura Aldohayan; Belinda Campos-Xavier; Delphine Bacq; Laurence Legeai-Mallet; Jacky Bonaventure; Arnold Munnich; Valérie Cormier-Daire
Journal:  Hum Genet       Date:  2002-03-13       Impact factor: 4.132

2.  Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing.

Authors:  J Körkkö; S Annunen; T Pihlajamaa; D J Prockop; L Ala-Kokko
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

3.  Revised diagnostic criteria for the Marfan syndrome.

Authors:  A De Paepe; R B Devereux; H C Dietz; R C Hennekam; R E Pyeritz
Journal:  Am J Med Genet       Date:  1996-04-24

4.  Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.

Authors:  M K Wirtz; J R Samples; P L Kramer; K Rust; J Yount; T S Acott; R D Koler; J Cisler; A Jahed; R J Gorlin; M Godfrey
Journal:  Am J Med Genet       Date:  1996-10-02

Review 5.  Marfan syndrome in the third Millennium.

Authors:  Gwenaëlle Collod-Béroud; Catherine Boileau
Journal:  Eur J Hum Genet       Date:  2002-11       Impact factor: 4.246

6.  Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions.

Authors:  J Körkkö; I Kaitila; L Lönnqvist; L Peltonen; L Ala-Kokko
Journal:  J Med Genet       Date:  2002-01       Impact factor: 6.318

7.  Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes.

Authors:  A Ganguly; M J Rock; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-01       Impact factor: 11.205

Review 8.  Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.

Authors:  Gwenaëlle Collod-Béroud; Saga Le Bourdelles; Lesley Ades; Leena Ala-Kokko; Patrick Booms; Maureen Boxer; Anne Child; Paolo Comeglio; Anne De Paepe; James C Hyland; Katerine Holman; Ilkka Kaitila; Bart Loeys; Gabor Matyas; Lieve Nuytinck; Leena Peltonen; Terhi Rantamaki; Peter Robinson; Beat Steinmann; Claudine Junien; Christophe Béroud; Catherine Boileau
Journal:  Hum Mutat       Date:  2003-09       Impact factor: 4.878

9.  Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes.

Authors:  B Lee; M Godfrey; E Vitale; H Hori; M G Mattei; M Sarfarazi; P Tsipouras; F Ramirez; D W Hollister
Journal:  Nature       Date:  1991-07-25       Impact factor: 49.962

10.  In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome.

Authors:  L Faivre; R J Gorlin; M K Wirtz; M Godfrey; N Dagoneau; J R Samples; M Le Merrer; G Collod-Beroud; C Boileau; A Munnich; V Cormier-Daire
Journal:  J Med Genet       Date:  2003-01       Impact factor: 6.318

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  5 in total

1.  Novel FBN1 mutations are responsible for cardiovascular manifestations of Marfan syndrome.

Authors:  Jin'e Wang; Yupeng Yan; Jinxing Chen; Ling Gong; Yu Zhang; Mengmeng Yuan; Bing Cui; Yibo Wang
Journal:  Mol Biol Rep       Date:  2016-08-24       Impact factor: 2.316

2.  C596G mutation in FBN1 causes Marfan syndrome with exotropia in a Chinese family.

Authors:  Fengyun Wang; Bo Li; Lan Lan; Lin Li
Journal:  Mol Vis       Date:  2015-02-23       Impact factor: 2.367

3.  Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis.

Authors:  Yijing Zhou; Dongwei Guo; Qianzhong Cao; Xinyu Zhang; Guangming Jin; Danying Zheng
Journal:  Mol Med Rep       Date:  2021-02-12       Impact factor: 2.952

4.  Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan Syndrome.

Authors:  Min-Rou Lin; Che-Mai Chang; Jafit Ting; Jan-Gowth Chang; Wan-Hsuan Chou; Kuei-Jung Huang; Gloria Cheng; Hsiao-Huang Chang; Wei-Chiao Chang
Journal:  J Pers Med       Date:  2022-02-01

Review 5.  The Molecular Genetics of Marfan Syndrome.

Authors:  Qiu Du; Dingding Zhang; Yue Zhuang; Qiongrong Xia; Taishen Wen; Haiping Jia
Journal:  Int J Med Sci       Date:  2021-05-27       Impact factor: 3.738

  5 in total

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