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A novel single-nucleotide substitution, Glu 4 Lys, in the leukotriene C4 synthase gene associated with allergic diseases.

Abstract
Cysteinyl leukotrienes (cysLTs) play important roles in bronchial asthma, and can mediate bronchial smooth muscle constriction and increase mucous secretion, vascular permeability and cellular infiltration. We identified a novel heterozygous single-nucleotide substitution 10G>A (Glu 4 Lys) in the first exon of the leukotriene C4 synthase gene (LTC4S). This substitution was detected in 5 of 141 allergic patients, but not in 110 nonallergic subjects. There was a difference in the Glu 4 Lys frequency between the allergic patients and nonallergic subjects (Fisher's exact test, p=0.0460). The five patients with Glu 4 Lys had allergic diseases such as bronchial asthma and/or allergic dermatitis. Furthermore, a familial analysis of Glu 4 Lys revealed a link with allergic diseases. Thus, our results suggest that Glu 4 Lys in the LTC4S might be associated with allergic diseases.
AuthorsKaori Yoshikawa, Eiko Matsui, Hideo Kaneko, Toshiyuki Fukao, Ryosuke Inoue, Takahide Teramoto, Shinji Shinoda, Osamu Fukutomi, Minako Aoki, Kimiko Kasahara, Naomi Kondo
JournalInternational journal of molecular medicine (Int J Mol Med) Vol. 16 Issue 5 Pg. 827-31 (Nov 2005) ISSN: 1107-3756 [Print] Greece
PMID16211251 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Glutamic Acid
  • Glutathione Transferase
  • leukotriene-C4 synthase
  • Lysine
Topics
  • Adolescent
  • Adult
  • Amino Acid Substitution (genetics)
  • Asthma (genetics)
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Dermatitis, Atopic (genetics)
  • Female
  • Glutamic Acid (genetics)
  • Glutathione Transferase (genetics)
  • Humans
  • Hypersensitivity, Immediate (genetics)
  • Infant
  • Lysine (genetics)
  • Male
  • Point Mutation
  • Respiratory Hypersensitivity (genetics)

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