Literature DB >> 15478097

A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia.

Mario Falchi1, Paola Forabosco, Evelina Mocci, Cesare Cappio Borlino, Andrea Picciau, Emanuela Virdis, Ivana Persico, Debora Parracciani, Andrea Angius, Mario Pirastu.   

Abstract

A powerful approach to mapping the genes for complex traits is to study isolated founder populations, in which genetic heterogeneity and environmental noise are likely to be reduced and in which extended genealogical data are often available. Using graph theory, we applied an approach that involved sampling from the large number of pairwise relationships present in an extended genealogy to reconstruct sets of subpedigrees that maximize the useful information for linkage mapping while minimizing calculation burden. We investigated, through simulation, the properties of the different sets in terms of bias in identity-by-descent (IBD) estimation and power decrease under various genetic models. We applied this approach to a small isolated population from Sardinia, the village of Talana, consisting of a unique large and complex pedigree, and performed a genomewide search through variance-components linkage analysis for serum lipid levels. We identified a region of significant linkage on chromosome 2 for total serum cholesterol and low-density lipoprotein (LDL) cholesterol. Through higher-density mapping, we obtained an increased linkage for both traits on 2q21.2-q24.1, with a LOD score of 4.3 for total serum cholesterol and of 3.9 for LDL cholesterol. A replication study was performed in an independent and larger set from a genetically differentiated isolated population of the same region of Sardinia, the village of Perdasdefogu. We obtained consistent linkage to the region for total serum cholesterol (LOD score 1.4) and LDL cholesterol (LOD score 2.2), with a level of concordance uncommon for complex traits, and refined the location of the quantitative-trait locus. Interestingly, the 2q21.1-22 region has also been linked to premature coronary heart disease in Finns, and, in the adjacent 2q14 region, significant linkage with triglycerides has been reported in Hutterites.

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Year:  2004        PMID: 15478097      PMCID: PMC1182138          DOI: 10.1086/426155

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  67 in total

1.  Replication of linkage studies of complex traits: an examination of variation in location estimates.

Authors:  S B Roberts; C J MacLean; M C Neale; L J Eaves; K S Kendler
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

Review 2.  Population choice in mapping genes for complex diseases.

Authors:  A F Wright; A D Carothers; M Pirastu
Journal:  Nat Genet       Date:  1999-12       Impact factor: 38.330

3.  WMA postpones decision to revise Declaration of Helsinki. World Medical Association.

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4.  Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.

Authors:  A Brooks-Wilson; M Marcil; S M Clee; L H Zhang; K Roomp; M van Dam; L Yu; C Brewer; J A Collins; H O Molhuizen; O Loubser; B F Ouelette; K Fichter; K J Ashbourne-Excoffon; C W Sensen; S Scherer; S Mott; M Denis; D Martindale; J Frohlich; K Morgan; B Koop; S Pimstone; J J Kastelein; J Genest; M R Hayden
Journal:  Nat Genet       Date:  1999-08       Impact factor: 38.330

Review 5.  Epidemiology and prevention of coronary heart disease in families.

Authors:  M Higgins
Journal:  Am J Med       Date:  2000-04-01       Impact factor: 4.965

6.  Allegro, a new computer program for multipoint linkage analysis.

Authors:  D F Gudbjartsson; K Jonasson; M L Frigge; A Kong
Journal:  Nat Genet       Date:  2000-05       Impact factor: 38.330

7.  Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population.

Authors:  S Acton; D Osgood; M Donoghue; D Corella; M Pocovi; A Cenarro; P Mozas; J Keilty; S Squazzo; E A Woolf; J M Ordovas
Journal:  Arterioscler Thromb Vasc Biol       Date:  1999-07       Impact factor: 8.311

Review 8.  APO E gene and gene-environment effects on plasma lipoprotein-lipid levels.

Authors:  J M Hagberg; K R Wilund; R E Ferrell
Journal:  Physiol Genomics       Date:  2000-12-18       Impact factor: 3.107

9.  Common hepatic lipase gene promoter variant determines clinical response to intensive lipid-lowering treatment.

Authors:  A Zambon; S S Deeb; B G Brown; J E Hokanson; J D Brunzell
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10.  Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.

Authors:  P Pajukanta; M Cargill; L Viitanen; I Nuotio; A Kareinen; M Perola; J D Terwilliger; E Kempas; M Daly; H Lilja; J D Rioux; T Brettin; J S Viikari; T Rönnemaa; M Laakso; E S Lander; L Peltonen
Journal:  Am J Hum Genet       Date:  2000-11-13       Impact factor: 11.043

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  20 in total

1.  Campora: a young genetic isolate in South Italy.

Authors:  Vincenza Colonna; Teresa Nutile; Maria Astore; Ombretta Guardiola; Giuliano Antoniol; Marina Ciullo; M Graziella Persico
Journal:  Hum Hered       Date:  2007-05-02       Impact factor: 0.444

2.  Linkage analysis with dense SNP maps in isolated populations.

Authors:  Céline Bellenguez; Carole Ober; Catherine Bourgain
Journal:  Hum Hered       Date:  2009-04-09       Impact factor: 0.444

3.  Identity-by-descent estimation and mapping of qualitative traits in large, complex pedigrees.

Authors:  Mark Abney
Journal:  Genetics       Date:  2008-07-13       Impact factor: 4.562

4.  Comparing population structure as inferred from genealogical versus genetic information.

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Journal:  Eur J Hum Genet       Date:  2009-06-24       Impact factor: 4.246

5.  Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.

Authors:  Weiva Sieh; Yoonha Choi; Nicola H Chapman; Ulla-Katrina Craig; Ellen J Steinbart; Joseph H Rothstein; Kiyomitsu Oyanagi; Ralph M Garruto; Thomas D Bird; Douglas R Galasko; Gerard D Schellenberg; Ellen M Wijsman
Journal:  Hum Mol Genet       Date:  2009-06-30       Impact factor: 6.150

6.  A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.

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Journal:  Bioinformatics       Date:  2012-11-18       Impact factor: 6.937

7.  A two-step genetic study on quantitative precursors of coronary artery disease in a homogeneous Indian population: case-control association discovery and validation by transmission-disequilibrium test.

Authors:  Sanjukta Mallik; Partha P Majumder
Journal:  J Biosci       Date:  2011-12       Impact factor: 1.826

8.  Identity by descent estimation with dense genome-wide genotype data.

Authors:  Lide Han; Mark Abney
Journal:  Genet Epidemiol       Date:  2011-07-18       Impact factor: 2.135

9.  A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.

Authors:  Fan Liu; Alejandro Arias-Vásquez; Kristel Sleegers; Yurii S Aulchenko; Manfred Kayser; Pascual Sanchez-Juan; Bing-Jian Feng; Aida M Bertoli-Avella; John van Swieten; Tatiana I Axenovich; Peter Heutink; Christine van Broeckhoven; Ben A Oostra; Cornelia M van Duijn
Journal:  Am J Hum Genet       Date:  2007-05-29       Impact factor: 11.025

10.  Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations.

Authors:  Evelina Mocci; Maria P Concas; Manuela Fanciulli; Nicola Pirastu; Mauro Adamo; Valentina Cabras; Cristina Fraumene; Ivana Persico; Alessandro Sassu; Andrea Picciau; Dionigio A Prodi; Donatella Serra; Ginevra Biino; Mario Pirastu; Andrea Angius
Journal:  BMC Med Genet       Date:  2009-08-28       Impact factor: 2.103

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