Innovations in phenotyping of mouse models in the German Mouse Clinic
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  • 作者:Helmut Fuchs (1)
    Valérie Gailus-Durner (1)
    Susanne Neschen (1)
    Thure Adler (1) (4)
    Luciana Caminha Afonso (1)
    Juan Antonio Aguilar-Pimentel (5) (6)
    Lore Becker (1) (7)
    Alexander Bohla (11)
    Julia Calzada-Wack (8)
    Christian Cohrs (1)
    Anna Dewert (1) (2)
    Barbara Fridrich (1)
    Lillian Garrett (9)
    Lisa Glasl (9)
    Alexander G?tz (11)
    Wolfgang Hans (1)
    Sabine M. H?lter (9)
    Marion Horsch (1)
    Anja Hurt (1)
    Eva Janas (8)
    Dirk Janik (8)
    Melanie Kahle (1)
    Martin Kistler (1) (2)
    Tanja Klein-Rodewald (8)
    Christoph Lengger (1)
    Tonia Ludwig (1)
    Holger Maier (1)
    Susan Marschall (1)
    Kateryna Micklich (1)
    Gabriele M?ller (1)
    Beatrix Naton (1)
    Cornelia Prehn (1)
    Oliver Puk (9)
    Ildikó Rácz (12)
    Michael R?? (1)
    Birgit Rathkolb (1) (3)
    Jan Rozman (1) (2)
    Markus Scheerer (1)
    Evelyn Schiller (1)
    Anja Schrewe (1)
    Ralph Steinkamp (1)
    Claudia St?ger (1)
    Minxuan Sun (9)
    Wilfried Szymczak (10)
    Irina Treise (1)
    Ingrid Liliana Vargas Panesso (1) (7)
    Alexandra M. Vernaleken (1) (7)
    Monja Willersh?user (1)
    Annemarie Wolff-Muscate (9)
    Ramona Zeh (1)
    Jerzy Adamski (1) (13)
    Johannes Beckers (1) (13)
    Raffi Bekeredjian (14)
    Dirk H. Busch (4)
    Oliver Eickelberg (11)
    Jack Favor (16)
    Jochen Graw (9)
    Heinz H?fler (15) (8)
    Christoph H?schen (10)
    Hugo Katus (14)
    Martin Klingenspor (2)
    Thomas Klopstock (7)
    Frauke Neff (8)
    Markus Ollert (5)
    Holger Schulz (18)
    Tobias St?ger (11)
    Eckhard Wolf (3)
    Wolfgang Wurst (17) (19) (20) (9)
    Ali ?nder Yildirim (11)
    Andreas Zimmer (12)
    Martin Hrabě de Angelis (1) (13) (21)
  • 刊名:Mammalian Genome
  • 出版年:2012
  • 出版时间:10 - October 2012
  • 年:2012
  • 卷:23
  • 期:9
  • 页码:611-622
  • 全文大小:851KB
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    3. Brown SD, Chambon P, Hrabé de Angelis M; Eumorphia Consortium (2005) EMPReSS: standardized phenotype screens for functional annotation of the mouse genome. Nat Genet 37(11):1155
    4. Du P, Ye L, Ruge F, Yang Y, Jiang WG (2011) Metastasis suppressor-1, MTSS1, acts as a putative tumour suppressor in human bladder cancer. Anticancer Res 31(10):3205-212
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    6. Fan H, Chen L, Zhang F, Quan Y, Su X, Qiu X, Zhao Z, Kong KL, Dong S, Song Y, Chan TH, Guan XY (2012) MTSS1, a novel target of DNA methyltransferase 3B, functions as a tumor suppressor in hepatocellular carcinoma. Oncogene 31(18):2298-308 CrossRef
    7. Friedel RH, Seisenberger C, Kaloff C, Wurst W (2007) EUCOMM-the European conditional mouse mutagenesis program. Brief Funct Genomic Proteomic 6(3):180-85 CrossRef
    8. Fuchs H, Gailus-Durner V, Adler T, Aguilar-Pimentel JA, Becker L, Calzada-Wack J, Da Silva-Buttkus P, Neff F, G?tz A, Hans W, H?lter SM, Horsch M, Kastenmüller G, Kemter E, Lengger C, Maier H, Matloka M, M?ller G, Naton B, Prehn C, Puk O, Rácz I, Rathkolb B, R?misch-Margl W, Rozman J, Wang-Sattler R, Schrewe A, St?ger C, Tost M, Adamski J, Aigner B, Beckers J, Behrendt H, Busch DH, Esposito I, Graw J, Illig T, Ivandic B, Klingenspor M, Klopstock T, Kremmer E, Mempel M, Neschen S, Ollert M, Schulz H, Suhre K, Wolf E, Wurst W, Zimmer A, Hrabě de Angelis M (2011) Mouse phenotyping. Methods 53(2):120-35 CrossRef
    9. Gailus-Durner V, Fuchs H, Becker L, Bolle I, Brielmeier M, Calzada-Wack J, Elvert R, Ehrhardt N, Dalke C, Franz TJ, Grundner-Culemann E, Hammelbacher S, H?lter SM, H?lzlwimmer G, Horsch M, Javaheri A, Kalaydjiev SV, Klempt M, Kling E, Kunder S, Lengger C, Lisse T, Mijalski T, Naton B, Pedersen V, Prehn C, Przemeck G, Rácz I, Reinhard C, Reitmeir P, Schneider I, Schrewe A, Steinkamp R, Zybill C, Adamski J, Beckers J, Behrendt H, Favor J, Graw J, Heldmaier G, H?fler H, Ivandic B, Katus H, Kirchhof P, Klingenspor M, Klopstock T, Lengeling A, Muller W, Ohl F, Ollert M, Quintanilla-Martinez L, Schmidt J, Schulz H, Wolf E, Wurst W, Zimmer A, Busch DH, Hrabé de Angelis M (2005) Introducing the German Mouse Clinic: open access platform for standardized phenotyping. Nat Methods 2(6):403-04 CrossRef
    10. G?tz AA, Rozman J, R?del HG, Fuchs H, Gailus-Durner V, Hrabě de Angelis M, Klingenspor M, Stoeger T (2011) Comparison of particle-exposure triggered pulmonary and systemic inflammation in mice fed with three different diets. Part Fibre Toxicol 8:30 CrossRef
    11. Hagn M, Marschall S, Hrabé de Angelis M (2007) EMMA-the European mouse mutant archive. Brief Funct Genomic Proteomic 6(3):186-92 CrossRef
    12. Haubenberger D, Reinthaler E, Mueller JC, Pirker W, Katzenschlager R, Froehlich R, Bruecke T, Daniel G, Auff E, Zimprich A (2011) Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson’s disease. Neurobiol Aging 32(2):302-07 CrossRef
    13. Horsch M, Sch?dler S, Gailus-Durner V, Fuchs H, Meyer H, Hrabé de Angelis M, Beckers J (2008) Systematic gene expression profiling of mouse model series reveals coexpressed genes. Proteomics 8(6):1248-256 CrossRef
    14. Kemter E, Rathkolb B, Rozman J, Hans W, Schrewe A, Landbrecht C, Klaften M, Ivandic B, Fuchs H, Gailus-Durner V, Klingenspor M, Hrabé de Angelis M, Wolf E, Wanke R, Aigner B (2009) Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism. Am J Physiol Renal Physiol 297(5):F1391–F1398 CrossRef
    15. Kemter E, Rathkolb B, Bankir L, Schrewe A, Hans W, Landbrecht C, Klaften M, Ivandic BT, Fuchs H, Gailus-Durner V, Hrabé de Angelis M, Wolf E, Wanke R, Aigner B (2010) Mutation of the Na+-K+-2Cl?/sup> cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia. Am J Physiol Renal Physiol 298(6):F1405–F1415 CrossRef
    16. Kleinschnitz C, Grund H, Wingler K, Armitage ME, Jones E, Mittal M, Barit D, Schwarz T, Geis C, Kraft P, Barthel K, Schuhmann MK, Herrmann AM, Meuth SG, Stoll G, Meurer S, Schrewe A, Becker L, Gailus-Durner V, Fuchs H, Klopstock T, Hrabé de Angelis M, Jandeleit-Dahm K, Shah AM, Weissmann N, Schmidt HH (2010) Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegeneration. PLoS Biol 8(9). pii: e1000479
    17. Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001) A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413:519-23 CrossRef
    18. Lhotta K (2010) Uromodulin and chronic kidney disease. Kidney Blood Press Res 33(5):393-98 CrossRef
    19. Li J, Dani JA, Le W (2009) The role of transcription factor Pitx3 in dopamine neuron development and Parkinson’s disease. Curr Top Med Chem 9(10):855-59
    20. Liu J, Sun QY, Tang BS, Hu L, Yu RH, Wang L, Shi CH, Yan XX, Pan Q, Xia K, Guo JF (2011) PITX3 gene polymorphism is associated with Parkinson’s disease in Chinese population. Brain Res 1392:116-20 CrossRef
    21. MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE (2005) Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet 76:1074-080 CrossRef
    22. Maier H, Lengger C, Simic B, Fuchs H, Gailus-Durner V, Hrabé de Angelis M (2008) MausDB: an open source application for phenotype data and mouse colony management in large-scale mouse phenotyping projects. BMC Bioinformatics 9:169 CrossRef
    23. Meyer CW, Klingenspor M, Rozman J, Heldmaier G (2004) Gene or size: metabolic rate and body temperature in obese growth hormone-deficient dwarf mice. Obes Res 12(9):1509-518 CrossRef
    24. Meyer CW, Neubronner J, Rozman J, Stumm G, Osanger A, Stoeger C, Augustin M, Grosse J, Klingenspor M, Heldmaier G (2007) Expanding the body mass range: associations between BMR and tissue morphology in wild type and mutant dwarf mice (David mice). J Comp Physiol B 177(2):183-92 CrossRef
    25. Raab M, Kappel S, Kr?mer A, Sanhaji M, Matthess Y, Kurunci-Csacsko E, Calzada-Wack J, Rathkolb B, Rozman J, Adler T, Busch DH, Esposito I, Fuchs H, Gailus-Durner V, Klingenspor M, Wolf E, S?nger N, Prinz F, Hrabé de Angelis M, Seibler J, Yuan J, Bergmann M, Knecht R, Kreft B, Strebhardt K (2011) Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells. Nat Commun 2:395 CrossRef
    26. Rosemann M, Ivashkevich A, Favor J, Dalke C, H?lter SM, Becker L, Rácz I, Bolle I, Klempt M, Rathkolb B, Kalaydjiev S, Adler T, Aguilar A, Hans W, Horsch M, Rozman J, Calzada-Wack J, Kunder S, Naton B, Gailus-Durner V, Fuchs H, Schulz H, Beck-ers J, Busch DH, Burbach JP, Smidt MP, Quintanilla-Martinez L, Esposito I, Klopstock T, Klingenspor M, Ollert M, Wolf E, Wurst W, Zimmer A, Hrabé de Angelis M, Atkinson M, Heinzmann U, Graw J (2010) Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 (416insG) mice. Mamm Genome 21(1-):13-7 CrossRef
    27. Saarikangas J, Mattila PK, Varjosalo M, Bovellan M, Hakanen J, Calzada-Wack J, Tost M, Jennen L, Rathkolb B, Hans W, Horsch M, Hyv?nen ME, Per?l? N, Fuchs H, Gailus-Durner V, Esposito I, Wolf E, Hrabé de Angelis M, Frilander MJ, Savilahti H, Sariola H, Sainio K, Lehtonen S, Taipale J, Salminen M, Lappalainen P (2011) Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia. J Cell Sci 124(Pt 8):1245-255 CrossRef
    28. Schneider I, Tirsch WS, Faus-Kessler T, Becker L, Kling E, Busse RL, Bender A, Feddersen B, Tritschler J, Fuchs H, Gailus-Durner V, Englmeier KH, Hrabé de Angelis M, Klopstock T (2006) Systematic, standardized and comprehensive neurological phenotyping of inbred mice strains in the German Mouse Clinic. J Neurosci Methods 157(1):82-0 CrossRef
    29. R Development Core Team (2010) R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing. ISBN 3-900051-07-0. http://www.R-project.org/. Accessed 12 Aug 2012
    30. Tocchetti A, Soppo CB, Zani F, Bianchi F, Gagliani MC, Pozzi B, Rozman J, Elvert R, Ehrhardt N, Rathkolb B, Moerth C, Horsch M, Fuchs H, Gailus-Durner V, Beckers J, Klingenspor M, Wolf E, Hrabé de Angelis M, Scanziani E, Tacchetti C, Scita G, Di Fiore PP, Offenh?user N (2010) Loss of the actin remodeler Eps8 causes intestinal defects and improved metabolic status in mice. PLoS One 5(3):e9468 CrossRef
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    32. Vyletal P, Bleyer AJ, Kmoch S (2010) Uromodulin biology and pathophysiology—an update. Kidney Blood Press Res 33(6):456-75 CrossRef
    33. Wang D, Xu MR, Wang T, Li T, Zhu J (2011) MTSS1 overexpression correlates with poor prognosis in colorectal cancer. J Gastrointest Surg 15(7):1205-212 CrossRef
    34. Xie F, Ye L, Chen J, Wu N, Zhang Z, Yang Y, Zhang L, Jiang WG (2011) The impact of metastasis suppressor-1, MTSS1, on oesophageal squamous cell carcinoma and its clinical significance. J Transl Med 9:95 CrossRef
    35. Yu D, Zhan XH, Niu S, Mikhailenko I, Strickland DK, Zhu J, Cao M, Zhan X (2011) Murine missing in metastasis (MIM) mediates cell polarity and regulates the motility response to growth factors. PLoS One 6(6):e20845 CrossRef
  • 作者单位:Helmut Fuchs (1)
    Valérie Gailus-Durner (1)
    Susanne Neschen (1)
    Thure Adler (1) (4)
    Luciana Caminha Afonso (1)
    Juan Antonio Aguilar-Pimentel (5) (6)
    Lore Becker (1) (7)
    Alexander Bohla (11)
    Julia Calzada-Wack (8)
    Christian Cohrs (1)
    Anna Dewert (1) (2)
    Barbara Fridrich (1)
    Lillian Garrett (9)
    Lisa Glasl (9)
    Alexander G?tz (11)
    Wolfgang Hans (1)
    Sabine M. H?lter (9)
    Marion Horsch (1)
    Anja Hurt (1)
    Eva Janas (8)
    Dirk Janik (8)
    Melanie Kahle (1)
    Martin Kistler (1) (2)
    Tanja Klein-Rodewald (8)
    Christoph Lengger (1)
    Tonia Ludwig (1)
    Holger Maier (1)
    Susan Marschall (1)
    Kateryna Micklich (1)
    Gabriele M?ller (1)
    Beatrix Naton (1)
    Cornelia Prehn (1)
    Oliver Puk (9)
    Ildikó Rácz (12)
    Michael R?? (1)
    Birgit Rathkolb (1) (3)
    Jan Rozman (1) (2)
    Markus Scheerer (1)
    Evelyn Schiller (1)
    Anja Schrewe (1)
    Ralph Steinkamp (1)
    Claudia St?ger (1)
    Minxuan Sun (9)
    Wilfried Szymczak (10)
    Irina Treise (1)
    Ingrid Liliana Vargas Panesso (1) (7)
    Alexandra M. Vernaleken (1) (7)
    Monja Willersh?user (1)
    Annemarie Wolff-Muscate (9)
    Ramona Zeh (1)
    Jerzy Adamski (1) (13)
    Johannes Beckers (1) (13)
    Raffi Bekeredjian (14)
    Dirk H. Busch (4)
    Oliver Eickelberg (11)
    Jack Favor (16)
    Jochen Graw (9)
    Heinz H?fler (15) (8)
    Christoph H?schen (10)
    Hugo Katus (14)
    Martin Klingenspor (2)
    Thomas Klopstock (7)
    Frauke Neff (8)
    Markus Ollert (5)
    Holger Schulz (18)
    Tobias St?ger (11)
    Eckhard Wolf (3)
    Wolfgang Wurst (17) (19) (20) (9)
    Ali ?nder Yildirim (11)
    Andreas Zimmer (12)
    Martin Hrabě de Angelis (1) (13) (21)

    1. German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    4. Institute for Medical Microbiology, Immunology, and Hygiene, TUM, Trogerstra?e 30, 81675, Munich, Germany
    5. Clinical Research Division of Molecular and Clinical Allergotoxicology, Department of Dermatology and Allergy, TUM, Biedersteiner Stra?e 29, 80802, Munich, Germany
    6. Division of Environmental Dermatology and Allergy TUM/Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    7. Department of Neurology, Friedrich-Baur-Institut, Ludwig-Maximilians-Universit?t München, Ziemssenstra?e 1a, 80336, Munich, Germany
    11. Comprehensive Pneumology Center, Institute of Lung Biology and Disease, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    8. Institute of Pathology, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    2. Molecular Nutritional Medicine, Else Kr?ner-Fresenius Center, TUM, Gregor-Mendel-Stra?e 2, 85350, Freising-Weihenstephan, Germany
    9. Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    12. Institute of Molecular Psychiatry, University of Bonn, Sigmund-Freud-Stra?e 25, 53105, Bonn, Germany
    3. Chair for Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-Universit?t München, Feodor Lynen-Stra?e 25, 81377, Munich, Germany
    10. Abteilung Medizinische Strahlenphysik und Diagnostik, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    13. Chair of Experimental Genetics, Center of Life and Food Sciences Weihenstephan, TUM, 85350, Freising-Weihenstephan, Germany
    14. Division of Cardiology, Department of Medicine III, University of Heidelberg, Otto-Meyerhof-Zentrum, Im Neuenheimer Feld 350, 69120, Heidelberg, Germany
    16. Institute of Human Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    15. Institute of Pathology, TUM, Ismaningerstra?e 22, 81675, Munich, Germany
    18. Institute of Epidemiology 1, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolst?dter Landstra?e 1, 85764, Neuherberg/Munich, Germany
    17. Chair of Developmental Genetics, TUM, Am Hochanger 8, 85350, Freising-Weihenstephan, Germany
    19. Max-Planck-Institute of Psychiatry, Kraepelinstra?e 2-10, 80804, Munich, Germany
    20. Deutsches Zentrum für Neurodegenerative Erkrankungen e. V. (DZNE) Site Munich, Schillerstra?e 44, 80336, Munich, Germany
    21. Member of German Center for Diabetes Research (DZD), 85764, Neuherberg, Germany
  • ISSN:1432-1777
文摘
Under the label of the German Mouse Clinic (GMC), a concept has been developed and implemented that allows the better understanding of human diseases on the pathophysiological and molecular level. This includes better understanding of the crosstalk between different organs, pleiotropy of genes, and the systemic impact of envirotypes and drugs. In the GMC, experts from various fields of mouse genetics and physiology, in close collaboration with clinicians, work side by side under one roof. The GMC is an open-access platform for the scientific community by providing phenotypic analysis in bilateral collaborations (“bottom-up projects- and as a partner and driver in international large-scale biology projects (“top-down projects-. Furthermore, technology development is a major topic in the GMC. Innovative techniques for primary and secondary screens are developed and implemented into the phenotyping pipelines (e.g., detection of volatile organic compounds, VOCs).

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