Large-scale mutagenesis of the mouse to understand the genetic bases of nervous system structure and function
N-ethyl- N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype...
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Published in | Brain research. Molecular brain research. Vol. 132; no. 2; pp. 105 - 115 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Amsterdam
Elsevier B.V
20.12.2004
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0169-328X 1872-6941 |
DOI | 10.1016/j.molbrainres.2004.09.016 |
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Abstract | N-ethyl-
N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype screens that assess nervous system structure and function. In particular, these screens focus on complex behavioral traits from drug and alcohol responses to circadian rhythms to epilepsy. Each of these centers has developed a bioinformatics infrastructure to track the extensive number of transactions that are inherent in these large-scale projects. Over 100 new mouse mutant lines have been defined through the efforts of these three mutagenesis centers and are presented to the research community via the centralized Web presence of the Neuromice.org consortium (
http://www.neuromice.org). This community resource provides visitors with the ability to search for specific mutant phenotypes, to view the genetic and phenotypic details of mutant mouse lines, and to order these mice for use in their own research program. |
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AbstractList | N-ethyl-N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype screens that assess nervous system structure and function. In particular, these screens focus on complex behavioral traits from drug and alcohol responses to circadian rhythms to epilepsy. Each of these centers has developed a bioinformatics infrastructure to track the extensive number of transactions that are inherent in these large-scale projects. Over 100 new mouse mutant lines have been defined through the efforts of these three mutagenesis centers and are presented to the research community via the centralized Web presence of the Neuromice.org consortium (
http://www.neuromice.org
). This community resource provides visitors with the ability to search for specific mutant phenotypes, to view the genetic and phenotypic details of mutant mouse lines, and to order these mice for use in their own research program. N-ethyl-N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype screens that assess nervous system structure and function. In particular, these screens focus on complex behavioral traits from drug and alcohol responses to circadian rhythms to epilepsy. Each of these centers has developed a bioinformatics infrastructure to track the extensive number of transactions that are inherent in these large-scale projects. Over 100 new mouse mutant lines have been defined through the efforts of these three mutagenesis centers and are presented to the research community via the centralized Web presence of the Neuromice.org consortium (http://www.neuromice.org). This community resource provides visitors with the ability to search for specific mutant phenotypes, to view the genetic and phenotypic details of mutant mouse lines, and to order these mice for use in their own research program.N-ethyl-N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype screens that assess nervous system structure and function. In particular, these screens focus on complex behavioral traits from drug and alcohol responses to circadian rhythms to epilepsy. Each of these centers has developed a bioinformatics infrastructure to track the extensive number of transactions that are inherent in these large-scale projects. Over 100 new mouse mutant lines have been defined through the efforts of these three mutagenesis centers and are presented to the research community via the centralized Web presence of the Neuromice.org consortium (http://www.neuromice.org). This community resource provides visitors with the ability to search for specific mutant phenotypes, to view the genetic and phenotypic details of mutant mouse lines, and to order these mice for use in their own research program. N-ethyl- N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype screens that assess nervous system structure and function. In particular, these screens focus on complex behavioral traits from drug and alcohol responses to circadian rhythms to epilepsy. Each of these centers has developed a bioinformatics infrastructure to track the extensive number of transactions that are inherent in these large-scale projects. Over 100 new mouse mutant lines have been defined through the efforts of these three mutagenesis centers and are presented to the research community via the centralized Web presence of the Neuromice.org consortium ( http://www.neuromice.org). This community resource provides visitors with the ability to search for specific mutant phenotypes, to view the genetic and phenotypic details of mutant mouse lines, and to order these mice for use in their own research program. N-ethyl-N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis Centers established for the detection of neuroscience-related phenotypes are described. Each center has developed an extensive panel of phenotype screens that assess nervous system structure and function. In particular, these screens focus on complex behavioral traits from drug and alcohol responses to circadian rhythms to epilepsy. Each of these centers has developed a bioinformatics infrastructure to track the extensive number of transactions that are inherent in these large-scale projects. Over 100 new mouse mutant lines have been defined through the efforts of these three mutagenesis centers and are presented to the research community via the centralized Web presence of the Neuromice.org consortium (http://www.neuromice.org). This community resource provides visitors with the ability to search for specific mutant phenotypes, to view the genetic and phenotypic details of mutant mouse lines, and to order these mice for use in their own research program. |
Author | Snoddy, Jay Frankel, Wayne N. Takahashi, Joseph S. Holtz-Vitaterna, Martha Pretel, Stephanie Swanson, Douglas J. Bult, Carol Yates, Jeana Goldowitz, Dan Kibbe, Warren A. Li, Yanxia |
AuthorAffiliation | d Oak Ridge National Laboratory, United States b The Jackson Laboratory, United States c Northwestern University, United States a Dept. Anatomy and Neurobiology, University of Tennessee Health Science Center, 855 Monroe Ave., Memphis, TN 38163, United States |
AuthorAffiliation_xml | – name: c Northwestern University, United States – name: d Oak Ridge National Laboratory, United States – name: b The Jackson Laboratory, United States – name: a Dept. Anatomy and Neurobiology, University of Tennessee Health Science Center, 855 Monroe Ave., Memphis, TN 38163, United States |
Author_xml | – sequence: 1 givenname: Dan surname: Goldowitz fullname: Goldowitz, Dan organization: Dept. Anatomy and Neurobiology, University of Tennessee Health Science Center, 855 Monroe Ave., Memphis, TN 38163, United States – sequence: 2 givenname: Wayne N. surname: Frankel fullname: Frankel, Wayne N. organization: The Jackson Laboratory, United States – sequence: 3 givenname: Joseph S. surname: Takahashi fullname: Takahashi, Joseph S. organization: Northwestern University, United States – sequence: 4 givenname: Martha surname: Holtz-Vitaterna fullname: Holtz-Vitaterna, Martha organization: Northwestern University, United States – sequence: 5 givenname: Carol surname: Bult fullname: Bult, Carol organization: The Jackson Laboratory, United States – sequence: 6 givenname: Warren A. surname: Kibbe fullname: Kibbe, Warren A. organization: Northwestern University, United States – sequence: 7 givenname: Jay surname: Snoddy fullname: Snoddy, Jay organization: Oak Ridge National Laboratory, United States – sequence: 8 givenname: Yanxia surname: Li fullname: Li, Yanxia organization: Northwestern University, United States – sequence: 9 givenname: Stephanie surname: Pretel fullname: Pretel, Stephanie organization: The Jackson Laboratory, United States – sequence: 10 givenname: Jeana surname: Yates fullname: Yates, Jeana organization: Northwestern University, United States – sequence: 11 givenname: Douglas J. surname: Swanson fullname: Swanson, Douglas J. email: dswanson@utmem.edu organization: Dept. Anatomy and Neurobiology, University of Tennessee Health Science Center, 855 Monroe Ave., Memphis, TN 38163, United States |
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Cites_doi | 10.1038/5012 10.1182/blood.V96.2.705 10.1242/dev.126.8.1601 10.1016/0027-5107(82)90225-1 10.1073/pnas.82.19.6619 10.1126/science.1069193 10.1038/nn0504-484 10.1007/s003350010095 10.1523/JNEUROSCI.23-05-01631.2003 10.1093/genetics/152.1.373 10.1073/pnas.95.13.7485 10.1007/s003350010093 10.1073/pnas.76.11.5818 10.1093/hmg/8.10.1955 |
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Keywords | N-ethyl- N-nitrosourea (ENU) Mouse mutants behavioral phenotype Neurogenetics Neural basis of behavior Functional genomics Vertebrata Mammalia N-ethyl-N-nitrosourea (ENU) Mouse Animal Rodentia Nervous system Behavior Mutation |
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References | Noveroske, Weber, Justice (bib11) 2000; 11 Rinchik, Russell (bib13) 1990; vol. I Russell, Kelly, Hunsicker, Bangham, Maddux, Phillips (bib16) 1979; 76 Battey, Jordan, Cox, Dove (bib1) 1999; 21 Bult, Kibbe, Snoddy, Vitaterna, Swanson, Pretel, Li, Hohman, Rinchik, Takahashi, Frankel, Goldowitz (bib2) 2004; 7 Lyon, Phillips, Fisher (bib9) 1982; 9 The Human Genome Issue Nature 409 (2003) 749–958. P. Isnard, N. Core, P. Naquet and M. Djabali, Altered lymphoid development in mice deficient for the mAF4 proto-oncogene. Blood. 96(2) 705–710 (Jul 15). Mural, Adams, Myers, Smith, Miklos, Wides, Halpern, Li, Sutton, Nadeau, Salzberg, Holt, Kodira, Lu, Chen, Deng, Evangelista, Gan, Heiman, Li, Li, Merkulov, Milshina, Naik, Qi, Shue, Wang, Wang, Wang, Yan, Y, Yooseph, Zhao, Zheng, Zhu, Biddick, Bolanos, Delcher, Dew, Fasulo, Flanigan, Huson, Kravitz, Miller, Mobarry, Reinert, Remington, Zhang, Zheng, Nusskern, Lai, Lei, Zhong, Yao, Guan, Ji, Gu, Wang, Zhong, Xiao, Chiang, Yandell, Wortman, Amanatides, Hladun, Pratts, Johnson, Dodson, Woodford, Evans, Gropman, Rusch, Venter, Wang, Smith, Houck, Tompkins, Haynes, Jacob, Chin, Allen, Dahlke, Sanders, Li, Liu, Levitsky, Majoros, Chen, Xia, Lopez, Donnelly, Newman, Glodek, Kraft, Nodell, Ali, An, Baldwin-Pitts, Beeson, Cai, Carnes, Carver, Caulk, Center, Chen, Cheng, Coyne, Crowder, Danaher, Davenport, Desilets, Dietz, Doup, Dullaghan, Ferriera, Fosler, Gire, Gluecksmann, Gocayne, Gray, Hart, Haynes, Hoover, Howland, Ibegwam, Jalali, Johns, Kline, Ma, MacCawley, Magoon, Mann, May, McIntosh, Mehta, Moy, Moy, Murphy, Murphy, Nelson, Nuri, Parker, Prudhomme, Puri, Qureshi, Raley, Reardon, Regier, Rogers, Romblad, Schutz, Scott, Scott, Sitter, Smallwood, Sprague, Stewart, Strong, Suh, Sylvester, Thomas, Tint, Tsonis, Wang, Wang, Williams, Williams, Windsor, Wolfe, Wu, Zaveri, Chaturvedi, Gabrielian, Ke, Sun, Subramanian, Venter, Pfannkoch, Barnstead, Stephenson (bib10) 2002; 296 Isaacs, Oliver, Jones, Jeans, Potter, Hovik, Nolan, Vizor, Glenister, Simon, Gray, Spurr, Brown, Hunter, Davies (bib6) 2003; 23 Rinchik, Carpenter (bib12) 1999; 152 The Human Genome Issue Science 291 (2003) 1145–1434. Hitotsumachi, Carpenter, Russell (bib4) 1985; 82 Roderick (bib15) 1983 Hentges, Thompson, P.A. (bib3) 1999; 126 Kasarskis, Manova, Anderson (bib8) 1998; 95 Rinchik (bib14) 2000; 11 Justice, Noveroske, Weber, Zheng, Bradley (bib7) 1999; 8 Lyon (10.1016/j.molbrainres.2004.09.016_bib9) 1982; 9 Rinchik (10.1016/j.molbrainres.2004.09.016_bib13) 1990; vol. I Isaacs (10.1016/j.molbrainres.2004.09.016_bib6) 2003; 23 10.1016/j.molbrainres.2004.09.016_bib5 Noveroske (10.1016/j.molbrainres.2004.09.016_bib11) 2000; 11 Roderick (10.1016/j.molbrainres.2004.09.016_bib15) 1983 Russell (10.1016/j.molbrainres.2004.09.016_bib16) 1979; 76 Mural (10.1016/j.molbrainres.2004.09.016_bib10) 2002; 296 Battey (10.1016/j.molbrainres.2004.09.016_bib1) 1999; 21 Bult (10.1016/j.molbrainres.2004.09.016_bib2) 2004; 7 Rinchik (10.1016/j.molbrainres.2004.09.016_bib14) 2000; 11 Rinchik (10.1016/j.molbrainres.2004.09.016_bib12) 1999; 152 Hitotsumachi (10.1016/j.molbrainres.2004.09.016_bib4) 1985; 82 Kasarskis (10.1016/j.molbrainres.2004.09.016_bib8) 1998; 95 Justice (10.1016/j.molbrainres.2004.09.016_bib7) 1999; 8 10.1016/j.molbrainres.2004.09.016_bib17 Hentges (10.1016/j.molbrainres.2004.09.016_bib3) 1999; 126 10.1016/j.molbrainres.2004.09.016_bib18 |
References_xml | – volume: 296 start-page: 1661 year: 2002 end-page: 1671 ident: bib10 article-title: A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome publication-title: Science – volume: vol. I start-page: 121 year: 1990 end-page: 158 ident: bib13 article-title: Germ-line deletion mutations in the mouse: tools for intensive functional and physical mapping of regions for the mammalian genome publication-title: Genome Analysis – volume: 7 start-page: 484 year: 2004 end-page: 485 ident: bib2 article-title: A genome end-game: understanding gene function in the nervous system publication-title: Nat. Neurosci. – volume: 11 start-page: 489 year: 2000 end-page: 499 ident: bib14 article-title: Developing genetic reagents to facilitate recovery, analysis, and maintenance of mouse mutations publication-title: Mamm. Genome – volume: 9 start-page: 217 year: 1982 end-page: 228 ident: bib9 article-title: Use of an inversion to test for induced X-linked lethals in mice publication-title: Mutat. Res. – volume: 152 start-page: 373 year: 1999 end-page: 383 ident: bib12 publication-title: Genetics – volume: 76 start-page: 5818 year: 1979 end-page: 5819 ident: bib16 article-title: Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse publication-title: Proc. Natl. Acad. Sci. U. S. A. – reference: The Human Genome Issue Science 291 (2003) 1145–1434. – volume: 82 start-page: 6619 year: 1985 end-page: 6621 ident: bib4 article-title: Dose-repetition increases the mutagenic effectiveness of publication-title: Proc. Natl. Acad. Sci. U. S. A. – volume: 8 start-page: 1955 year: 1999 end-page: 1963 ident: bib7 article-title: Mouse ENU mutagenesis publication-title: Hum. Mol. Genet. – start-page: 135 year: 1983 end-page: 167 ident: bib15 article-title: Using inversions to detect and study recessive lethals and detrimentals in mice publication-title: Utilization of Mammalian Specific-Locus Studies in Hazard Evaluation and Estimation of Genetic Risk – volume: 21 start-page: 73 year: 1999 end-page: 75 ident: bib1 article-title: An action plan for mouse genomics publication-title: Nat. Genet. – volume: 11 start-page: 478 year: 2000 end-page: 483 ident: bib11 article-title: The mutagenic action of publication-title: Mamm. Genome – reference: P. Isnard, N. Core, P. Naquet and M. Djabali, Altered lymphoid development in mice deficient for the mAF4 proto-oncogene. Blood. 96(2) 705–710 (Jul 15). – volume: 95 start-page: 7485 year: 1998 end-page: 7490 ident: bib8 article-title: A phenotype-based screen for embryonic lethal mutations in the mouse publication-title: Proc. Natl. Acad. Sci. U. S. A. – reference: The Human Genome Issue Nature 409 (2003) 749–958. – volume: 126 start-page: 1601 year: 1999 end-page: 1609 ident: bib3 article-title: The publication-title: Development – volume: 23 start-page: 1631 year: 2003 end-page: 1637 ident: bib6 article-title: A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse publication-title: J. Neurosci. – volume: 21 start-page: 73 year: 1999 ident: 10.1016/j.molbrainres.2004.09.016_bib1 article-title: An action plan for mouse genomics publication-title: Nat. Genet. doi: 10.1038/5012 – ident: 10.1016/j.molbrainres.2004.09.016_bib5 doi: 10.1182/blood.V96.2.705 – volume: 126 start-page: 1601 year: 1999 ident: 10.1016/j.molbrainres.2004.09.016_bib3 article-title: The flat-top gene is required for the expansion and regionalization of the telencephalic primordium publication-title: Development doi: 10.1242/dev.126.8.1601 – volume: 9 start-page: 217 year: 1982 ident: 10.1016/j.molbrainres.2004.09.016_bib9 article-title: Use of an inversion to test for induced X-linked lethals in mice publication-title: Mutat. Res. doi: 10.1016/0027-5107(82)90225-1 – volume: 82 start-page: 6619 year: 1985 ident: 10.1016/j.molbrainres.2004.09.016_bib4 article-title: Dose-repetition increases the mutagenic effectiveness of N-ethyl-N-nitrosourea in mouse spermatogonia publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.82.19.6619 – volume: 296 start-page: 1661 year: 2002 ident: 10.1016/j.molbrainres.2004.09.016_bib10 article-title: A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome publication-title: Science doi: 10.1126/science.1069193 – volume: 7 start-page: 484 year: 2004 ident: 10.1016/j.molbrainres.2004.09.016_bib2 article-title: A genome end-game: understanding gene function in the nervous system publication-title: Nat. Neurosci. doi: 10.1038/nn0504-484 – volume: 11 start-page: 489 year: 2000 ident: 10.1016/j.molbrainres.2004.09.016_bib14 article-title: Developing genetic reagents to facilitate recovery, analysis, and maintenance of mouse mutations publication-title: Mamm. Genome doi: 10.1007/s003350010095 – start-page: 135 year: 1983 ident: 10.1016/j.molbrainres.2004.09.016_bib15 article-title: Using inversions to detect and study recessive lethals and detrimentals in mice – volume: 23 start-page: 1631 year: 2003 ident: 10.1016/j.molbrainres.2004.09.016_bib6 article-title: A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.23-05-01631.2003 – volume: vol. I start-page: 121 year: 1990 ident: 10.1016/j.molbrainres.2004.09.016_bib13 article-title: Germ-line deletion mutations in the mouse: tools for intensive functional and physical mapping of regions for the mammalian genome – volume: 152 start-page: 373 year: 1999 ident: 10.1016/j.molbrainres.2004.09.016_bib12 article-title: N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah–Hbb Interval of mouse chromosome 7: completed testing of 4,557 gametes and deletion mapping and complementation analysis of 31 mutations publication-title: Genetics doi: 10.1093/genetics/152.1.373 – ident: 10.1016/j.molbrainres.2004.09.016_bib17 – ident: 10.1016/j.molbrainres.2004.09.016_bib18 – volume: 95 start-page: 7485 year: 1998 ident: 10.1016/j.molbrainres.2004.09.016_bib8 article-title: A phenotype-based screen for embryonic lethal mutations in the mouse publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.95.13.7485 – volume: 11 start-page: 478 year: 2000 ident: 10.1016/j.molbrainres.2004.09.016_bib11 article-title: The mutagenic action of N-ethyl-N-nitrosourea in the mouse publication-title: Mamm. Genome doi: 10.1007/s003350010093 – volume: 76 start-page: 5818 year: 1979 ident: 10.1016/j.molbrainres.2004.09.016_bib16 article-title: Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.76.11.5818 – volume: 8 start-page: 1955 year: 1999 ident: 10.1016/j.molbrainres.2004.09.016_bib7 article-title: Mouse ENU mutagenesis publication-title: Hum. Mol. Genet. doi: 10.1093/hmg/8.10.1955 |
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N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis... N-ethyl-N-nitrosourea (ENU) mutagenesis is presented as a powerful approach to developing models for human disease. The efforts of three NIH Mutagenesis... |
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SubjectTerms | Alkylating Agents Animals Biological and medical sciences Ethylnitrosourea Functional genomics Fundamental and applied biological sciences. Psychology Mice Mouse mutants behavioral phenotype Mutagenesis N-ethyl- N-nitrosourea (ENU) Nervous System Diseases - genetics Nervous System Physiological Phenomena Neurogenetics Vertebrates: nervous system and sense organs |
Title | Large-scale mutagenesis of the mouse to understand the genetic bases of nervous system structure and function |
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