Literature DB >> 16799019

No VSX1 gene mutations associated with keratoconus.

Anthony J Aldave1, Vivek S Yellore, Andrew K Salem, Gina L Yoo, Sylvia A Rayner, Huiying Yang, George Y Tang, Yoana Piconell, Yaron S Rabinowitz.   

Abstract

PURPOSE: To determine whether mutations of the VSX1 gene play a pathogenetic role in the development of keratoconus (KTCN).
METHODS: DNA extraction, PCR amplification, and direct sequencing of the VSX1 gene were performed in 100 unrelated patients with diagnoses of clinical and topographic features of KTCN.
RESULTS: Of the four previously identified presumed pathogenic mutations in the VSX1 gene (Leu17Pro, Asp144Glu, Leu159Met, and Arg166Trp), only Asp144Glu was identified in a single affected patient. Two novel single nucleotide polymorphisms (SNPs), both resulting in synonymous substitutions, were identified: c.53G>T (Ser6Ser) in four affected patients and c.209G>T (Pro58Pro) in two affected patients. Two previously reported SNPs were also identified: c.426C>A (Arg131Ser) in one affected patient and c.581A>G (Ala182Ala) in 51 of the 100 affected patients.
CONCLUSIONS: Only one of the presumed pathogenic mutations in the VSX1 gene, Asp144Glu, was identified in a single member of the cohort of affected patients. However, as previously demonstrated, Asp144Glu is a non-disease-causing polymorphism. The absence of pathogenic mutations in the VSX1 gene in a large number of unrelated KTCN patients indicates that other genetic factors are involved in the development of this disorder.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16799019     DOI: 10.1167/iovs.05-1530

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  39 in total

1.  Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus.

Authors:  Kathryn P Burdon; Stuart Macgregor; Yelena Bykhovskaya; Sharhbanou Javadiyan; Xiaohui Li; Kate J Laurie; Dorota Muszynska; Richard Lindsay; Judith Lechner; Talin Haritunians; Anjali K Henders; Durga Dash; David Siscovick; Seema Anand; Anthony Aldave; Douglas J Coster; Loretta Szczotka-Flynn; Richard A Mills; Sudha K Iyengar; Kent D Taylor; Tony Phillips; Grant W Montgomery; Jerome I Rotter; Alex W Hewitt; Shiwani Sharma; Yaron S Rabinowitz; Colin Willoughby; Jamie E Craig
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-10-31       Impact factor: 4.799

2.  Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Authors:  Kathryn P Burdon; Douglas J Coster; Jac C Charlesworth; Richard A Mills; Kate J Laurie; Cecilia Giunta; Alex W Hewitt; Paul Latimer; Jamie E Craig
Journal:  Hum Genet       Date:  2008-09-05       Impact factor: 4.132

3.  Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening.

Authors:  Anthony J Aldave; Lydia B Ann; Ricardo F Frausto; Catherine K Nguyen; Fei Yu; Irving M Raber
Journal:  JAMA Ophthalmol       Date:  2013-12       Impact factor: 7.389

4.  Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.

Authors:  Marta Czugala; Justyna A Karolak; Dorota M Nowak; Piotr Polakowski; Jose Pitarque; Andrea Molinari; Malgorzata Rydzanicz; Bassem A Bejjani; Beatrice Y J T Yue; Jacek P Szaflik; Marzena Gajecka
Journal:  Eur J Hum Genet       Date:  2011-11-02       Impact factor: 4.246

5.  VSX1 gene analysis in keratoconus.

Authors:  Mukesh Tanwar; Manoj Kumar; Bhagabat Nayak; Dhananjay Pathak; Namrata Sharma; Jeewan S Titiyal; Rima Dada
Journal:  Mol Vis       Date:  2010-11-16       Impact factor: 2.367

6.  Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus.

Authors:  Justyna A Karolak; Karolina Kulinska; Dorota M Nowak; Jose A Pitarque; Andrea Molinari; Malgorzata Rydzanicz; Bassem A Bejjani; Marzena Gajecka
Journal:  Mol Vis       Date:  2011-03-30       Impact factor: 2.367

7.  An association between the calpastatin (CAST) gene and keratoconus.

Authors:  Xiaohui Li; Yelena Bykhovskaya; Yongming G Tang; Yoana Picornell; Talin Haritunians; Anthony J Aldave; Loretta Szczotka-Flynn; Sudha K Iyengar; Jerome I Rotter; Kent D Taylor; Yaron S Rabinowitz
Journal:  Cornea       Date:  2013-05       Impact factor: 2.651

8.  VSX1 gene variants are associated with keratoconus in unrelated Korean patients.

Authors:  Jee-Won Mok; Sun-Jin Baek; Choun-Ki Joo
Journal:  J Hum Genet       Date:  2008-07-15       Impact factor: 3.172

9.  Molecular analysis of the VSX1 gene in familial keratoconus.

Authors:  Petra Liskova; Neil D Ebenezer; Pirro G Hysi; Rhian Gwilliam; Mohamed F El-Ashry; Lalitha C Moodaley; Scott Hau; Michael Twa; Stephen J Tuft; Shomi S Bhatacharya
Journal:  Mol Vis       Date:  2007-10-04       Impact factor: 2.367

10.  A novel VSX1 mutation identified in an individual with keratoconus in India.

Authors:  Preeti Paliwal; Anuradha Singh; Radhika Tandon; Jeevan S Titiyal; Arundhati Sharma
Journal:  Mol Vis       Date:  2009-11-28       Impact factor: 2.367

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.