A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
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  • 作者:Michelle M Simon (1)
    Simon Greenaway (1)
    Jacqueline K White (2)
    Helmut Fuchs (3)
    Valérie Gailus-Durner (3)
    Sara Wells (1)
    Tania Sorg (6)
    Kim Wong (2)
    Elodie Bedu (6)
    Elizabeth J Cartwright (7)
    Romain Dacquin (9)
    Sophia Djebali (9)
    Jeanne Estabel (2)
    Jochen Graw (4)
    Neil J Ingham (2)
    Ian J Jackson (10)
    Andreas Lengeling (11)
    Silvia Mandillo (12)
    Jacqueline Marvel (9)
    Hamid Meziane (6)
    Frédéric Preitner (13)
    Oliver Puk (4)
    Michel Roux (6)
    David J Adams (2)
    Sarah Atkins (1)
    Abdel Ayadi (6)
    Lore Becker (3)
    Andrew Blake (1)
    Debra Brooker (1)
    Heather Cater (1)
    Marie-France Champy (6)
    Roy Combe (6)
    Petr Danecek (2)
    Armida di Fenza (1)
    Hilary Gates (1)
    Anna-Karin Gerdin (2)
    Elisabetta Golini (12)
    John M Hancock (1)
    Wolfgang Hans (3)
    Sabine M H?lter (3)
    Tertius Hough (1)
    Pierre Jurdic (9)
    Thomas M Keane (2)
    Hugh Morgan (1)
    Werner Müller (8)
    Frauke Neff (5)
    George Nicholson (1)
    Bastian Pasche (14)
    Laura-Anne Roberson (2)
    Jan Rozman (3)
    Mark Sanderson (2)
    Luis Santos (1)
    Mohammed Selloum (6)
    Carl Shannon (2)
    Anne Southwell (1)
    Glauco P Tocchini-Valentini (12)
    Valerie E Vancollie (2)
    Henrik Westerberg (1)
    Wolfgang Wurst (16) (17) (18) (4)
    Min Zi (7)
    Binnaz Yalcin (15) (6)
    Ramiro Ramirez-Solis (2)
    Karen P Steel (2)
    Ann-Marie Mallon (1)
    Martin Hrabě de Angelis (3)
    Yann Herault (6)
    Steve DM Brown (1)
  • 关键词:Mouse inbred lines ; sequence variation ; mouse phenotyping ; gene knockout ; C57BL/6
  • 刊名:Genome Biology
  • 出版年:2013
  • 出版时间:July 2013
  • 年:2013
  • 卷:14
  • 期:7
  • 全文大小:1,267 KB
  • 参考文献:1. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A: A conditional knockout resource for the genome-wide study of mouse gene function. / Nature 2011, 474:337-42. CrossRef
    2. Brown SD, Moore MW: Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium. / Dis Model Mech 2012, 5:289-92. CrossRef
    3. Carneiro AM, Airey DC, Thompson B, Zhu CB, Lu L, Chesler EJ, Erikson KM, Blakely RD: Functional coding variation in recombinant inbred mouse lines reveals multiple serotonin transporter-associated phenotypes. / Proc Natl Acad Sci USA 2009, 106:2047-052. CrossRef
    4. Williams RW, Gu J, Qi S, Lu L: The genetic structure of recombinant inbred mice: high-resolution consensus maps for complex trait analysis. / Genome Biol 2001, 2:RESEARCH0046.
    5. Gregorova S, Divina P, Storchova R, Trachtulec Z, Fotopulosova V, Svenson KL, Donahue LR, Paigen B, Forejt J: Mouse consomic strains: exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies. / Genome Res 2008, 18:509-15. CrossRef
    6. Valdar W, Solberg LC, Gauguier D, Burnett S, Klenerman P, Cookson WO, Taylor MS, Rawlins JN, Mott R, Flint J: Genome-wide genetic association of complex traits in heterogeneous stock mice. / Nat Genet 2006, 38:879-87. CrossRef
    7. Churchill GA, Airey DC, Allayee H, Angel JM, Attie AD, Beatty J, Beavis WD, Belknap JK, Bennett B, Berrettini W, Bleich A, Bogue M, Broman KW, Buck KJ, Buckler E, Burmeister M, Chesler EJ, Cheverud JM, Clapcote S, Cook MN, Cox RD, Crabbe JC, Crusio WE, Darvasi A, Deschepper CF, Doerge RW, Farber CR, Forejt J, Gaile D, Garlow SJ, / et al.: The Collaborative Cross, a community resource for the genetic analysis of complex traits. / Nat Genet 2004, 36:1133-137. CrossRef
    8. Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, Barlow K, Beck S, Berry E, Birren B, Bloom T, Bork P, Botcherby M, Bray N, Brent MR, Brown DG, Brown SD, Bult C, Burton J, Butler J, Campbell RD, Carninci P, / et al.: Initial sequencing and comparative analysis of the mouse genome. / Nature 2002, 420:520-62. CrossRef
    9. Church DM, Goodstadt L, Hillier LW, Zody MC, Goldstein S, She X, Bult CJ, Agarwala R, Cherry JL, DiCuccio M, Hlavina W, Kapustin Y, Meric P, Maglott D, Birtle Z, Marques AC, Graves T, Zhou S, Teague B, Potamousis K, Churas C, Place M, Herschleb J, Runnheim R, Forrest D, Amos-Landgraf J, Schwartz DC, Cheng Z, Lindblad-Toh K, Eichler EE, / et al.: Lineage-specific biology revealed by a finished genome assembly of the mouse. / PLoS Biol 2009, 7:e1000112. CrossRef
    10. Mekada K, Abe K, Murakami A, Nakamura S, Nakata H, Moriwaki K, Obata Y, Yoshiki A: Genetic differences among C57BL/6 substrains. / Exp Anim 2009, 58:141-49. CrossRef
    11. Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, Heger A, Agam A, Slater G, Goodson M, Furlotte NA, Eskin E, Nellaker C, Whitley H, Cleak J, Janowitz D, Hernandez-Pliego P, Edwards A, Belgard TG, Oliver PL, McIntyre RE, Bhomra A, Nicod J, Gan X, Yuan W, van der Weyden L, Steward CA, Bala S, Stalker J, Mott R, / et al.: Mouse genomic variation and its effect on phenotypes and gene regulation. / Nature 2011, 477:289-94. CrossRef
    12. DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ: A framework for variation discovery and genotyping using next-generation DNA sequencing data. / Nat Genet 2011, 43:491-98. CrossRef
    13. Gnerre S, Maccallum I, Przybylski D, Ribeiro FJ, Burton JN, Walker BJ, Sharpe T, Hall G, Shea TP, Sykes S, Berlin AM, Aird D, Costello M, Daza R, Williams L, Nicol R, Gnirke A, Nusbaum C, Lander ES, Jaffe DB: High-quality draft assemblies of mammalian genomes from massively parallel sequence data. / Proc Natl Acad Sci USA 2011, 108:1513-518. CrossRef
    14. Wang K, Li M, Hakonarson H: ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. / Nucleic Acids Res 2010, 38:e164. CrossRef
    15. Grant JR, Arantes AS, Liao X, Stothard P: In-depth annotation of SNPs arising from resequencing projects using NGS-SNP. / Bioinformatics 2011, 27:2300-301. CrossRef
    16. Wong K, Keane TM, Stalker J, Adams DJ: Enhanced structural variant and breakpoint detection using SVMerge by integration of multiple detection methods and local assembly. / Genome Biol 2010, 11:R128. CrossRef
    17. Yalcin B, Wong K, Bhomra A, Goodson M, Keane TM, Adams DJ, Flint J: The fine-scale architecture of structural variants in 17 mouse genomes. / Genome Biol 2012, 13:R18. CrossRef
    18. Freeman H, Shimomura K, Horner E, Cox RD, Ashcroft FM: Nicotinamide nucleotide transhydrogenase: a key role in insulin secretion. / Cell metabolism 2006, 3:35-5. CrossRef
    19. Morgan H, Beck T, Blake A, Gates H, Adams N, Debouzy G, Leblanc S, Lengger C, Maier H, Melvin D, Meziane H, Richardson D, Wells S, White J, Wood J, de Angelis MH, Brown SD, Hancock JM, Mallon AM: EuroPhenome: a repository for high-throughput mouse phenotyping data. / Nucleic Acids Res 2010, 38:D577-85. CrossRef
    20. Gates H, Mallon AM, Brown SD: High-throughput mouse phenotyping. / Methods 2011, 53:394-04. CrossRef
    21. Prusky GT, Alam NM, Beekman S, Douglas RM: Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system. / Invest Ophthalmol Vis Sci 2004, 45:4611-616. vs.04-0541" target="_blank" title="It opens in new window">CrossRef
    22. Mattapallil MJ, Wawrousek EF, Chan CC, Zhao H, Roychoudhury J, Ferguson TA, Caspi RR: The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes. / Invest Ophthalmol Vis Sci 2012, 53:2921-927. vs.12-9662" target="_blank" title="It opens in new window">CrossRef
    23. Paques M, Guyomard JL, Simonutti M, Roux MJ, Picaud S, Legargasson JF, Sahel JA: Panretinal, high-resolution color photography of the mouse fundus. / Invest Ophthalmol Vis Sci 2007, 48:2769-774. vs.06-1099" target="_blank" title="It opens in new window">CrossRef
    24. Matsuo N, Takao K, Nakanishi K, Yamasaki N, Tanda K, Miyakawa T: Behavioral profiles of three C57BL/6 substrains. / Front Behav Neurosci 2010, 4:29.
    25. Tucci V, Lad HV, Parker A, Polley S, Brown SD, Nolan PM: Gene-environment interactions differentially affect mouse strain behavioral parameters. / Mamm Genome 2006, 17:1113-120. CrossRef
    26. Grenham S, Clarke G, Cryan JF, Dinan TG: Brain-gut-microbe communication in health and disease. / Front Physiol 2011, 2:94. CrossRef
    27. Mehalow AK, Kameya S, Smith RS, Hawes NL, Denegre JM, Young JA, Bechtold L, Haider NB, Tepass U, Heckenlively JR, Chang B, Naggert JK, Nishina PM: CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina. / Human molecular genetics 2003, 12:2179-189. CrossRef
    28. Choi Y, Sims GE, Murphy S, Miller JR, Chan AP: Predicting the functional effect of amino Acid substitutions and indels. / PLoS One 2012, 7:e46688. CrossRef
    29. Jeru I, Duquesnoy P, Fernandes-Alnemri T, Cochet E, Yu JW, Lackmy-Port-Lis M, Grimprel E, Landman-Parker J, Hentgen V, Marlin S, McElreavey K, Sarkisian T, Grateau G, Alnemri ES, Amselem S: Mutations in NALP12 cause hereditary periodic fever syndromes. / Proc Natl Acad Sci USA 2008, 105:1614-619. CrossRef
    30. Arthur JC, Lich JD, Ye Z, Allen IC, Gris D, Wilson JE, Schneider M, Roney KE, O'Connor BP, Moore CB, Morrison A, Sutterwala FS, Bertin J, Koller BH, Liu Z, Ting JP: Cutting edge: NLRP12 controls dendritic and myeloid cell migration to affect contact hypersensitivity. / J Immunol 2010, 185:4515-519. CrossRef
    31. SNP & Indel Data [v/projects/SNP/snp_viewTable.cgi?handle=MRCHARWELL" class="a-plus-plus">http://www.ncbi.nlm.nih.gov/projects/SNP/snp_viewTable.cgi?handle=MRCHARWELL]
    32. Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, Smigielski EM, Sirotkin K: dbSNP: the NCBI database of genetic variation. / Nucleic Acids Res 2001, 29:308-11. CrossRef
    33. Manske HM, Kwiatkowski DP: LookSeq: a browser-based viewer for deep sequencing data. / Genome Res 2009, 19:2125-132. CrossRef
    34. Yalcin B, Willis-Owen SA, Fullerton J, Meesaq A, Deacon RM, Rawlins JN, Copley RR, Morris AP, Flint J, Mott R: Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice. / Nat Genet 2004, 36:1197-202. CrossRef
    35. Structural Variant Data [va/page.php" class="a-plus-plus">http://www.ebi.ac.uk/dgva/page.php]
    36. Eppig JT, Blake JA, Bult CJ, Kadin JA, Richardson JE: The Mouse Genome Database (MGD): comprehensive resource for genetics and genomics of the laboratory mouse. / Nucleic Acids Res 2012, 40:D881-86. CrossRef
    37. Mallon AM, Blake A, Hancock JM: EuroPhenome and EMPReSS: online mouse phenotyping resource. / Nucleic Acids Res 2008, 36:D715-18. CrossRef
    38. Europhenome Java Library [http://sourceforge.net/projects/europhenome/]
    39. Phenotype Data [http://www.har.mrc.ac.uk/nj]
    40. Efron B: 1977 Rietz Lecture: Bootstrap methods - another look at the jackknife. / Ann Stat 1979, 7:1-6. CrossRef
  • 作者单位:Michelle M Simon (1)
    Simon Greenaway (1)
    Jacqueline K White (2)
    Helmut Fuchs (3)
    Valérie Gailus-Durner (3)
    Sara Wells (1)
    Tania Sorg (6)
    Kim Wong (2)
    Elodie Bedu (6)
    Elizabeth J Cartwright (7)
    Romain Dacquin (9)
    Sophia Djebali (9)
    Jeanne Estabel (2)
    Jochen Graw (4)
    Neil J Ingham (2)
    Ian J Jackson (10)
    Andreas Lengeling (11)
    Silvia Mandillo (12)
    Jacqueline Marvel (9)
    Hamid Meziane (6)
    Frédéric Preitner (13)
    Oliver Puk (4)
    Michel Roux (6)
    David J Adams (2)
    Sarah Atkins (1)
    Abdel Ayadi (6)
    Lore Becker (3)
    Andrew Blake (1)
    Debra Brooker (1)
    Heather Cater (1)
    Marie-France Champy (6)
    Roy Combe (6)
    Petr Danecek (2)
    Armida di Fenza (1)
    Hilary Gates (1)
    Anna-Karin Gerdin (2)
    Elisabetta Golini (12)
    John M Hancock (1)
    Wolfgang Hans (3)
    Sabine M H?lter (3)
    Tertius Hough (1)
    Pierre Jurdic (9)
    Thomas M Keane (2)
    Hugh Morgan (1)
    Werner Müller (8)
    Frauke Neff (5)
    George Nicholson (1)
    Bastian Pasche (14)
    Laura-Anne Roberson (2)
    Jan Rozman (3)
    Mark Sanderson (2)
    Luis Santos (1)
    Mohammed Selloum (6)
    Carl Shannon (2)
    Anne Southwell (1)
    Glauco P Tocchini-Valentini (12)
    Valerie E Vancollie (2)
    Henrik Westerberg (1)
    Wolfgang Wurst (16) (17) (18) (4)
    Min Zi (7)
    Binnaz Yalcin (15) (6)
    Ramiro Ramirez-Solis (2)
    Karen P Steel (2)
    Ann-Marie Mallon (1)
    Martin Hrabě de Angelis (3)
    Yann Herault (6)
    Steve DM Brown (1)

    1. Medical Research Council Harwell (Mammalian Genetics Unit and Mary Lyon Centre), Harwell Science Campus, OX11 0RD, Kragujevac, UK
    2. The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, CB10 1SA, UK
    3. Helmholtz Zentrum München, German Research Centre for Environmental Health, Institute of Experimental Genetics and German Mouse Clinic, Ingolst?dter Landstra?e 1, Neuherberg, D-85764, Germany
    6. Institut Clinique de la Souris, ICS/MCI, PHENOMIN, GIE CERBM, IGBMC, CNRS, INSERM, 1 Rue Laurent Fries, 67404, Illkirch-Graffenstaden Cedex, France
    7. Faculty of Medical and Human Sciences, University of Manchester, Oxford Road, Manchester, MN13 9PT, UK
    9. AniRA ImmOs phenotyping facility- SFR Biosciences Lyon Gerland- UMS3444/US8, 21 avenue Tony Garnier, F-69007, Lyon, France
    4. Helmholtz Zentrum München, German Research Centre for Environmental Health, Institute of Developmental Genetics, Ingolst?dter Landstra?e 1, Neuherberg, D-85764, Germany
    10. Medical Research Council Human Genetics Unit, IGMM, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK
    11. Infection and Immunity Division, Roslin Institute, University of Edinburgh, Easter Bush Veterinary Campus, Midlothian, EH25 9RG, UK
    12. Consiglio Nazionale delle Ricerche- Cell Biology and Neurobiology Institute, Via E.Ramarini 32, 00015, Monterotondo Scala, Italy
    13. Department of Infection Genetics, Helmholtz Centre for Infection Research, Inhoffenstra?e 7, Braunschweig, 38124, Germany
    8. Faculty of Life Sciences, University of Manchester, Oxford Road, Manchester, MN13 9PT, UK
    5. Helmholtz Zentrum München, German Research Centre for Environmental Health, Institute of Pathology, Ingolst?dter Landstra?e 1, Neuherberg, D-85764, Germany
    14. Mouse Metabolic Facility of the Cardiomet Center, University Hospital, and Center for Integrative Genomics, University of Lausanne, 1015, Lausanne, Switzerland
    16. Chair for Developmental Genetics, Technische Universit?t München, Arcisstr. 21, Munich, 80333, Germany
    17. Max Planck Institute of Psychiatry, Kraepelinstrasse 2, Munich, 80804, Germany
    18. Deutsches Zentrum für Neurodegenerative Erkrankungen, Schillerstrasse 44, Munich, 80336, Germany
    15. Center for Integrative Genomics, University of Lausanne, Lausanne, CH-1015, Switzerland
  • ISSN:1465-6906
文摘
Background The mouse inbred line C57BL/6J is widely used in mouse genetics and its genome has been incorporated into many genetic reference populations. More recently large initiatives such as the International Knockout Mouse Consortium (IKMC) are using the C57BL/6N mouse strain to generate null alleles for all mouse genes. Hence both strains are now widely used in mouse genetics studies. Here we perform a comprehensive genomic and phenotypic analysis of the two strains to identify differences that may influence their underlying genetic mechanisms. Results We undertake genome sequence comparisons of C57BL/6J and C57BL/6N to identify SNPs, indels and structural variants, with a focus on identifying all coding variants. We annotate 34 SNPs and 2 indels that distinguish C57BL/6J and C57BL/6N coding sequences, as well as 15 structural variants that overlap a gene. In parallel we assess the comparative phenotypes of the two inbred lines utilizing the EMPReSSslim phenotyping pipeline, a broad based assessment encompassing diverse biological systems. We perform additional secondary phenotyping assessments to explore other phenotype domains and to elaborate phenotype differences identified in the primary assessment. We uncover significant phenotypic differences between the two lines, replicated across multiple centers, in a number of physiological, biochemical and behavioral systems. Conclusions Comparison of C57BL/6J and C57BL/6N demonstrates a range of phenotypic differences that have the potential to impact upon penetrance and expressivity of mutational effects in these strains. Moreover, the sequence variants we identify provide a set of candidate genes for the phenotypic differences observed between the two strains.

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