Literature DB >> 15852006

Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains.

David J Adams1, Emmanouil T Dermitzakis, Tony Cox, James Smith, Rob Davies, Ruby Banerjee, James Bonfield, James C Mullikin, Yeun Jun Chung, Jane Rogers, Allan Bradley.   

Abstract

Inbred mouse strains provide the foundation for mouse genetics. By selecting for phenotypic features of interest, inbreeding drives genomic evolution and eliminates individual variation, while fixing certain sets of alleles that are responsible for the trait characteristics of the strain. Mouse strains 129Sv (129S5) and C57BL/6J, two of the most widely used inbred lines, diverged from common ancestors within the last century, yet very little is known about the genomic differences between them. By comparative genomic hybridization and sequence analysis of 129S5 short insert libraries, we identified substantial structural variation, a complex fine-scale haplotype pattern with a continuous distribution of diversity blocks, and extensive nucleotide variation, including nonsynonymous coding SNPs and stop codons. Collectively, these genomic changes denote the level and direction of allele fixation that has occurred during inbreeding and provide a basis for defining what makes these mouse strains unique.

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Year:  2005        PMID: 15852006     DOI: 10.1038/ng1551

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  30 in total

1.  Variation in CCL3L1 copy number in rhesus macaques (Macaca mulatta).

Authors:  Patrick L Taormina; Jessica A Satkoski Trask; David G Smith; Sreetharan Kanthaswamy
Journal:  Comp Med       Date:  2012-06       Impact factor: 0.982

2.  Segmental copy number variation shapes tissue transcriptomes.

Authors:  Charlotte N Henrichsen; Nicolas Vinckenbosch; Sebastian Zöllner; Evelyne Chaignat; Sylvain Pradervand; Frédéric Schütz; Manuel Ruedi; Henrik Kaessmann; Alexandre Reymond
Journal:  Nat Genet       Date:  2009-03-08       Impact factor: 38.330

3.  The evolution of meiosis from mitosis.

Authors:  Adam S Wilkins; Robin Holliday
Journal:  Genetics       Date:  2009-01       Impact factor: 4.562

4.  A catalog of nonsynonymous polymorphism on mouse chromosome 16.

Authors:  Jeffrey M Kidd; Karrie C Trevarthen; David L Tefft; Ze Cheng; Michaele Mooney; Mark D Adams
Journal:  Mamm Genome       Date:  2005-12-08       Impact factor: 2.957

5.  Biochemical, molecular and behavioral phenotypes of Rab3A mutations in the mouse.

Authors:  S Yang; M Farias; D Kapfhamer; J Tobias; G Grant; T Abel; M Bućan
Journal:  Genes Brain Behav       Date:  2007-02       Impact factor: 3.449

6.  Analysis of copy number variations among diverse cattle breeds.

Authors:  George E Liu; Yali Hou; Bin Zhu; Maria Francesca Cardone; Lu Jiang; Angelo Cellamare; Apratim Mitra; Leeson J Alexander; Luiz L Coutinho; Maria Elena Dell'Aquila; Lou C Gasbarre; Gianni Lacalandra; Robert W Li; Lakshmi K Matukumalli; Dan Nonneman; Luciana C de A Regitano; Tim P L Smith; Jiuzhou Song; Tad S Sonstegard; Curt P Van Tassell; Mario Ventura; Evan E Eichler; Tara G McDaneld; John W Keele
Journal:  Genome Res       Date:  2010-03-08       Impact factor: 9.043

7.  Lgals6, a 2-million-year-old gene in mice: a case of positive Darwinian selection and presence/absence polymorphism.

Authors:  Denis Houzelstein; Isabelle R Gonçalves; Annie Orth; François Bonhomme; Pierre Netter
Journal:  Genetics       Date:  2008-03       Impact factor: 4.562

8.  Copy number variation in the bovine genome.

Authors:  João Fadista; Bo Thomsen; Lars-Erik Holm; Christian Bendixen
Journal:  BMC Genomics       Date:  2010-05-06       Impact factor: 3.969

9.  Widespread duplications in the genomes of laboratory stocks of Dictyostelium discoideum.

Authors:  Gareth Bloomfield; Yoshimasa Tanaka; Jason Skelton; Alasdair Ivens; Robert R Kay
Journal:  Genome Biol       Date:  2008-04-22       Impact factor: 13.583

10.  Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.

Authors:  Melissa K Boles; Bonney M Wilkinson; Laurens G Wilming; Bin Liu; Frank J Probst; Jennifer Harrow; Darren Grafham; Kathryn E Hentges; Lanette P Woodward; Andrea Maxwell; Karen Mitchell; Michael D Risley; Randy Johnson; Karen Hirschi; James R Lupski; Yosuke Funato; Hiroaki Miki; Pablo Marin-Garcia; Lucy Matthews; Alison J Coffey; Anne Parker; Tim J Hubbard; Jane Rogers; Allan Bradley; David J Adams; Monica J Justice
Journal:  PLoS Genet       Date:  2009-12-11       Impact factor: 5.917

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