Literature DB >> 11687514

A novel mutation in the M1S1 gene responsible for gelatinous droplike corneal dystrophy.

G Tasa1, J Kals, K Muru, E Juronen, A Piirsoo, S Veromann, S Jänes, A V Mikelsaar, A Lang.   

Abstract

PURPOSE: To identify the genetic defect in the M1S1 gene causing gelatinous droplike corneal dystrophy (GDLD) in an Estonian family.
METHODS: DNA was extracted from members of a GDLD-affected family and control persons. Polymerase chain reaction followed by direct sequencing was used to detect mutations in the M1S1 gene. Sequencing results were confirmed with restriction analysis.
RESULTS: Sequencing of the M1S1 gene revealed a novel mutation and a common polymorphism. All patients with GDLD were found to be homozygous for the insertion of nucleotide C in position 520 in M1S1. The mutation leads to formation of truncated protein. The mutation was excluded in 103 normal, unaffected individuals. Very close to the location where the mutation was identified in the M1S1 gene, a single-nucleotide polymorphism (518A/C) was found, changing aspartic acid to alanine at codon 173.
CONCLUSIONS: The data indicate that mutation ins520C in the M1S1 gene is the primary cause of GDLD in the family studied.

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Year:  2001        PMID: 11687514

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


  8 in total

1.  Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea.

Authors:  K Araki-Sasaki; Y Ando; M Nakamura; K Kitagawa; S Ikemizu; T Kawaji; T Yamashita; M Ueda; K Hirano; M Yamada; K Matsumoto; S Kinoshita; H Tanihara
Journal:  Br J Ophthalmol       Date:  2005-06       Impact factor: 4.638

2.  Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient.

Authors:  Bei Zhang; Yu-Feng Yao
Journal:  Mol Vis       Date:  2010-08-11       Impact factor: 2.367

Review 3.  The IC3D classification of the corneal dystrophies.

Authors:  Jayne S Weiss; H U Møller; Walter Lisch; Shigeru Kinoshita; Anthony J Aldave; Michael W Belin; Tero Kivelä; Massimo Busin; Francis L Munier; Berthold Seitz; John Sutphin; Cecilie Bredrup; Mark J Mannis; Christopher J Rapuano; Gabriel Van Rij; Eung Kweon Kim; Gordon K Klintworth
Journal:  Cornea       Date:  2008-12       Impact factor: 2.651

4.  Two novel mutations of TACSTD2 found in three Japanese gelatinous drop-like corneal dystrophy families with their aberrant subcellular localization.

Authors:  Mina Nakatsukasa; Satoshi Kawasaki; Kenta Yamasaki; Hideki Fukuoka; Akira Matsuda; Kohji Nishida; Shigeru Kinoshita
Journal:  Mol Vis       Date:  2011-04-19       Impact factor: 2.367

5.  Novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy.

Authors:  Passara Jongkhajornpong; Kaevalin Lekhanont; Mayumi Ueta; Koji Kitazawa; Satoshi Kawasaki; Shigeru Kinoshita
Journal:  Hum Genome Var       Date:  2015-11-26

6.  Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD).

Authors:  Elham Alehabib; Javad Jamshidi; Hamid Ghaedi; Babak Emamalizadeh; Monavvar Andarva; Narsis Daftarian; Mozhgan Rezaei Kanavi; Peyman Mohammadi Torbati; Goldis Espandar; Somayeh Alinaghi; Amir Hossein Johari; Mansoor Saghally; Fatemeh Mohajerani; Hossein Darvish
Journal:  Int J Mol Cell Med       Date:  2017-12-11

7.  Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families.

Authors:  Bei Zhang; Yu-Feng Yao; Ping Zhou
Journal:  Mol Vis       Date:  2007-06-24       Impact factor: 2.367

8.  A novel mutation in gelatinous drop-like corneal dystrophy and functional analysis.

Authors:  Yukiko Nagahara; Motokazu Tsujikawa; Toru Takigawa; Peng Xu; Chifune Kai; Satoshi Kawasaki; Mina Nakatsukasa; Tsutomu Inatomi; Shigeru Kinoshita; Kohji Nishida
Journal:  Hum Genome Var       Date:  2019-07-11
  8 in total

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