Literature DB >> 16738036

Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene.

C Brasch-Andersen1, Q Tan, A D Børglum, A Haagerup, T R Larsen, J Vestbo, T A Kruse.   

Abstract

BACKGROUND: Asthma is a complex genetic disorder. Many studies have suggested that chromosome 12q harbours a susceptibility gene for asthma and atopy. Linkage on chromosome 12q24.21-q24.33 was investigated in 167 Danish families with asthma.
METHODS: A two step procedure was used: (1) a genome-wide scan in one set of families followed by (2) fine scale mapping in an independent set of families in candidate regions with a maximum likelihood score (MLS) of > or =1.5 in the genome-wide scan. Polymorphisms in a candidate gene in the region on 12q24.33 were tested for association with asthma in a family based transmission disequilibrium test.
RESULTS: An MLS of 3.27 was obtained at 12q24.33. The significance of this result was tested by simulation, resulting in a significant empirical genome-wide p value of 0.018. To our Knowledge, this is the first significant evidence for linkage on chromosome 12q, and suggests a candidate region distal to most previously reported regions. Three single nucleotide polymorphisms in splicing factor, arginine/serine-rich 8 (SFRS8) had an association with asthma (p < or = 0.0020-0.050) in a sample of 136 asthmatic sib pairs. SFRS8 regulates the splicing of CD45, a protein which, through alternative splice variants, has an essential role in activating T cells. T cells are involved in the pathogenesis of atopic diseases such as asthma, so SFRS8 is a very interesting candidate gene in the region.
CONCLUSIONS: Linkage and simulation studies show that the very distal part of chromosome 12q contains a gene that increases the susceptibility to asthma. SFRS8 could act as a weak predisposing gene for asthma in our sample.

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Year:  2006        PMID: 16738036      PMCID: PMC2104763          DOI: 10.1136/thx.2005.055475

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  36 in total

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Authors:  Y Yokouchi; Y Nukaga; M Shibasaki; E Noguchi; K Kimura; S Ito; M Nishihara; K Yamakawa-Kobayashi; K Takeda; N Imoto; K Ichikawa; A Matsui; H Hamaguchi; T Arinami
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3.  Genome screen for asthma and related phenotypes in the French EGEA study.

Authors:  M H Dizier; C Besse-Schmittler; M Guilloud-Bataille; I Annesi-Maesano; M Boussaha; J Bousquet; D Charpin; A Degioanni; F Gormand; A Grimfeld; J Hochez; G Hyne; A Lockhart; M Luillier-Lacombe; R Matran; F Meunier; F Neukirch; Y Pacheco; V Parent; E Paty; I Pin; C Pison; P Scheinmann; N Thobie; D Vervloet; F Kauffmann; J Feingold; M Lathrop; F Demenais
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Authors:  K C Barnes; L R Freidhoff; R Nickel; Y F Chiu; S H Juo; N Hizawa; R P Naidu; E Ehrlich; D L Duffy; C Schou; P N Levett; D G Marsh; T H Beaty
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Authors:  Emiko Noguchi; Yukako Yokouchi; Jiang Zhang; Kazuko Shibuya; Akira Shibuya; Makoto Bannai; Katsushi Tokunaga; Hitomi Doi; Mayumi Tamari; Makiko Shimizu; Taro Shirakawa; Masanao Shibasaki; Kunio Ichikawa; Tadao Arinami
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Review 8.  The role of lymphocytes in allergic disease.

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9.  Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children.

Authors:  G Malerba; M C Lauciello; T Scherpbier; E Trabetti; R Galavotti; V Cusin; L Pescollderungg; G Zanoni; L C Martinati; A L Boner; R C Levitt; P F Pignatti
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  8 in total

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2.  Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.

Authors:  Juan C Celedón; Manuel E Soto-Quiros; Lydiana Avila; Stephen L Lake; Catherine Liang; Eduardo Fournier; Mitzi Spesny; Craig P Hersh; Jody S Sylvia; Thomas J Hudson; Andrei Verner; Barbara J Klanderman; Nelson B Freimer; Edwin K Silverman; Scott T Weiss
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Review 4.  Integrating genomic and clinical medicine: searching for susceptibility genes in complex lung diseases.

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Journal:  Transl Res       Date:  2007-12-18       Impact factor: 7.012

5.  Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource.

Authors:  Craig C Teerlink; Nicola J Camp; Aruna Bansal; Robert Crapo; Dana Hughes; Edward Kort; Kerry Rowe; Lisa A Cannon-Albright
Journal:  Eur J Hum Genet       Date:  2008-12-17       Impact factor: 4.246

6.  Genetic variability in susceptibility to occupational respiratory sensitization.

Authors:  Berran Yucesoy; Victor J Johnson
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7.  Family-Based Association Study of Pulmonary Function in a Population in Northeast Asia.

Authors:  Ho-Young Son; Seong-Wook Sohn; Sun-Hwa Im; Hyun-Jin Kim; Mi Kyeong Lee; Bayasgalan Gombojav; Hyouk-Soo Kwon; Daniel S Park; Hyung-Lae Kim; Kyung-Up Min; Joohon Sung; Jeong-Sun Seo; Jong-Il Kim
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8.  Splicing factor arginine/serine-rich 8 promotes multiple myeloma malignancy and bone lesion through alternative splicing of CACYBP and exosome-based cellular communication.

Authors:  Yuanjiao Zhang; Xichao Yu; Rongze Sun; Jie Min; Xiaozhu Tang; Zigen Lin; Siyuan Xie; Xinying Li; Shengfeng Lu; Zhidan Tian; Chunyan Gu; Lesheng Teng; Ye Yang
Journal:  Clin Transl Med       Date:  2022-02
  8 in total

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