用户名: 密码: 验证码:
The assessment of inter-individual variation of whole-genome DNA sequence in 32 cows
详细信息    查看全文
  • 作者:Joanna Szyda ; Magdalena Fr?szczak ; Magda Mielczarek ; Riccardo Giannico…
  • 刊名:Mammalian Genome
  • 出版年:2015
  • 出版时间:December 2015
  • 年:2015
  • 卷:26
  • 期:11-12
  • 页码:658-665
  • 全文大小:802 KB
  • 参考文献:Baes CF, Dolezal MA, Koltes JE, Bapst B, Fritz-Waters E, Jansen S, Flury C, Signer-Hasler H, Stricker C, Fernando R, Fries R, Moll J, Garrick DJ, Reecy JM, Gredler B (2014) Evaluation of variant identification methods for whole genome sequencing data in dairy cattle. BMC Genom 15:948CrossRef
    Bolger AM, Lohse M, Usadel B (2014) Trimmomatic: a flexible trimmer for illumina sequence data. Bioinformatics 30:2114-120PubMedCentral CrossRef PubMed
    Br?ndum RF, Guldbrandtsen B, Sahana G, Lund MS, Su G (2014) Strategies for imputation to whole genome sequence using a single or multi
    eed reference population in cattle. BMC Genom 15:728CrossRef
    Daetwyler HD, Capitan A, Pausch H, Stothard P, van Binsbergen R, Br?ndum RF, Liao X, Djari A, Rodriguez SC, Grohs C, Esquerré D, Bouchez O, Rossignol MN, Klopp C, Rocha D, Fritz S, Eggen A, Bowman PJ, Coote D, Chamberlain AJ, Anderson C, VanTassell CP, Hulsegge I, Goddard ME, Guldbrandtsen B, Lund MS, Veerkamp RF, Boichard DA, Fries R, Hayes BJ (2014) Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle. Nat Genet 46:858-65CrossRef PubMed
    Eck SH, Benet-Pagès A, Flisikowski K, Meitinger T, Fries R, Strom TM (2009) Whole genome sequencing of a single Bos taurus animal for single nucleotide polymorphism discovery. Genome Biol 10:R82PubMedCentral CrossRef PubMed
    H?glund J, Guldbrandtsen B, Lund MS, Sahana G (2015) Identification of genomic regions associated with female fertility in Danish Jersey using whole genome sequence data. BMC Genet 16:60PubMedCentral CrossRef PubMed
    Hong X, Scofield DG, Lynch M (2006) Intron size, abundance, and distribution within untranslated regions of genes. Mol Biol Evol 23:2392-404CrossRef PubMed
    Jansen S, Aigner B, Pausch H, Wysocki M, Eck S, Benet-Pagès A, Graf E, Wieland T, Strom TM, Meitinger T, Fries R (2013) Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage. BMC Genom 14:446CrossRef
    K?ks S, Lilleoja R, Reimann E, Salumets A, Reemann P, Jaakma ü (2013) Sequencing and annotated analysis of the Holstein cow genome. Mamm Genome 24:309-21CrossRef PubMed
    K?ks S, Reimann E, Lilleoja R, L?ttekivi F, Salumets A, Reemann P, Jaakma ü (2014) Sequencing and annotated analysis of full genome of Holstein breed bull. Mamm Genome 25:363-73CrossRef PubMed
    Larizza A, Makalowski W, Pesole G, Saccone C (2002) Evolutionary dynamics of mammalian mRNA untranslated regions by comparative analysis of orthologous human, artiodactyl and rodent gene pairs. Comput Chem 26:479-90CrossRef PubMed
    Larkin DM, Daetwyler HD, Hernandez AG, Wright CL, Hetrick LA, Boucek L, Bachman SL, Band MR, Akraiko TV, Cohen-Zinder M, Thimmapuram J, Macleod IM, Harkins TT, McCague JE, Goddard ME, Hayes BJ, Lewin HA (2012) Whole-genome resequencing of two elite sires for the detection of haplotypes under selection in dairy cattle. Proc Nat Acad Sci USA 109:7693-698PubMedCentral CrossRef PubMed
    Lee KT, Chung WH, Lee SY, Choi JW, Kim J, Lim D, Lee S, Jang GW, Kim B, Choy YH, Liao X, Stothard P, Moore SS, Lee SH, Ahn S, Kim N, Kim TH (2013) Whole-genome resequencing of Hanwoo (Korean cattle) and insight into regions of homozygosity. BMC Genom 14:519CrossRef
    Li H (2014) Towards better understanding of artifacts in variant calling from high-coverage samples. Bioinformatics 30:2843-851PubMedCentral CrossRef PubMed
    Li H, Durbin R (2010) Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 26:589-95PubMedCentral CrossRef PubMed
    Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R, 1000 Genome Project Data Processing Subgroup (2009) The sequence alignment/map (SAM) format and SAM tools. Bioinformatics 25:2078-079PubMedCentral CrossRef PubMed
    McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, DePristo MA (2010) The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20:1297-303PubMedCentral CrossRef PubMed
    Mignone F, Gissi C, Liuni S, Pesole G (2002) Untranslated regions of mRNAs. Genome Biol 3:REVIEWS0004
    Ptashne M, Gann A (2001) Transcription initiation: imposing specificity by localization. Essays Biochem 37:1-5CrossRef PubMed
    Stothard P, Choi JW, Basu U, Sumner-Thomson JM, Meng Y, Liao X, Moore SS (2011) Whole genome resequencing of black Angus and Holstein cattle for SNP and CNV discovery. BMC Genome 12:559CrossRef
    Wilkie GS, Dickson KS, Gray NK (2003) Regulation of mRNA translation by 5- and 3-UTR-binding factors. Trends Biochem Sci 28:182-88CrossRef PubMed
  • 作者单位:Joanna Szyda (1)
    Magdalena Fr?szczak (1)
    Magda Mielczarek (1)
    Riccardo Giannico (2)
    Giulietta Minozzi (2) (3)
    Ezequiel L. Nicolazzi (2)
    Stanislaw Kamiński (4)
    Katarzyna Wojdak-Maksymiec (5)

    1. Biostatistics Group, Department of Genetics, Wroclaw University of Environmental and Life Sciences, Kozuchowska 7, 51-631, Wroclaw, Poland
    2. Fondazione Parco Tecnologico Padano, Via Einstein Albert, 26900, Lodi, LO, Italy
    3. DIVET, Università di Milano, Via Celoria 10, 20133, Milan, Italy
    4. Institute of Animal Genetics, University of Warmia and Mazury, Oczapowskiego 2, Olsztyn, 10-719, Poland
    5. West Pomeranian University of Technology, Piastów 17, 70-310, Szczecin, Poland
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Cell Biology
    Anatomy
    Zoology
  • 出版者:Springer New York
  • ISSN:1432-1777
文摘
Despite the growing number of sequenced bovine genomes, the knowledge of the population-wide variation of sequences remains limited. In many studies, statistical methodology was not applied in order to relate findings in the sequenced samples to a population-wide level. Our goal was to assess the population-wide variation in DNA sequence based on whole-genome sequences of 32 Holstein–Friesian cows. The number of SNPs significantly varied across individuals. The number of identified SNPs increased with coverage, following a logarithmic curve. A total of 15,272,427 SNPs were identified, 99.16 % of them being bi-allelic. Missense SNPs were classified into three categories based on their genomic location: housekeeping genes, genes undergoing strong selection, and genes neutral to selection. The number of missense SNPs was significantly higher within genes neutral to selection than in the other two categories. The number of variants located within 3′UTR and 5′UTR regions was also significantly different across gene families. Moreover, the number of insertions and deletions differed significantly among cows varying between 261,712 and 330,103 insertions and from 271,398 to 343,649 deletions. Results not only demonstrate inter-individual variation in the number of SNPs and indels but also show that the number of missense SNPs differs across genes representing different functional backgrounds.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700