TY - JOUR
T1 - Genome-wide, large-scale production of mutant mice by ENU mutagenesis
AU - De Angelis, Martin Hrabé
AU - Flaswinkel, Heinrich
AU - Fuchs, Helmut
AU - Rathkolb, Birgit
AU - Soewarto, Dian
AU - Marschall, Susan
AU - Heffner, Stephan
AU - Pargent, Walter
AU - Wuensch, Kurt
AU - Jung, Martin
AU - Reis, André
AU - Richter, Thomas
AU - Alessandrini, Francesca
AU - Jakob, Thilo
AU - Fuchs, Edith
AU - Kolb, Helmut
AU - Kremmer, Elisabeth
AU - Schaeble, Karlheinz
AU - Rollinski, Boris
AU - Roscher, Adelbert
AU - Peters, Christoph
AU - Meitinger, Thomas
AU - Strom, Tim
AU - Steckler, Thomas
AU - Holsboer, Florian
AU - Klopstock, Thomas
AU - Gekeler, Florian
AU - Schindewolf, Catherine
AU - Jung, Thomas
AU - Avraham, Karen
AU - Behrendt, Heidrun
AU - Ring, Johannes
AU - Zimmer, Andreas
AU - Schughart, Klaus
AU - Pfeffer, Klaus
AU - Wolf, Eckhard
AU - Balling, Rudi
N1 - Funding Information:
We thank A. Servatius, S. Prettin, G. Bergter, N. Hirsch, A. Mayer, S. Manz, S. Hoffmann, F. Golla, B. Beneckenstein, K. Lobenwein, A. Wolf and D. Kreitz for technical assistance; C. Schindewolf for comments and revision of the manuscript; and H. Wagner for support. Part of this project was supported by grants from the German Human Genome Project to R.B., E.W. and M.H.d.A. (01KW9610/1), and to K.P., J.R. and H.B. (01KW9636).
PY - 2000
Y1 - 2000
N2 - In the post-genome era, the mouse will have a major role as a model system for functional genome analysis. This requires a large number of mutants similar to the collections available from other model organisms such as Drosophila melanogaster and Caenorhabditis elegans. Here we report on a systematic, genome-wide, mutagenesis screen in mice. As part of the German Human Genome Project, we have undertaken a large-scale ENU-mutagenesis screen for dominant mutations and a limited screen for recessive mutations. In screening over 14,000 mice for a large number of clinically relevant parameters, we recovered 182 mouse mutants for a variety of phenotypes. In addition, 247 variant mouse mutants are currently in genetic confirmation testing and will result in additional new mutant lines. This mutagenesis screen, along with the screen described in the accompanying paper, leads to a significant increase in the number of mouse models available to the scientific community. Our mutant lines are freely accessible to non-commercial users (for information, see http://www.gsf.de/ieg/groups/enu-mouse.html).
AB - In the post-genome era, the mouse will have a major role as a model system for functional genome analysis. This requires a large number of mutants similar to the collections available from other model organisms such as Drosophila melanogaster and Caenorhabditis elegans. Here we report on a systematic, genome-wide, mutagenesis screen in mice. As part of the German Human Genome Project, we have undertaken a large-scale ENU-mutagenesis screen for dominant mutations and a limited screen for recessive mutations. In screening over 14,000 mice for a large number of clinically relevant parameters, we recovered 182 mouse mutants for a variety of phenotypes. In addition, 247 variant mouse mutants are currently in genetic confirmation testing and will result in additional new mutant lines. This mutagenesis screen, along with the screen described in the accompanying paper, leads to a significant increase in the number of mouse models available to the scientific community. Our mutant lines are freely accessible to non-commercial users (for information, see http://www.gsf.de/ieg/groups/enu-mouse.html).
UR - http://www.scopus.com/inward/record.url?scp=0034425715&partnerID=8YFLogxK
U2 - 10.1038/78146
DO - 10.1038/78146
M3 - Article
C2 - 10932192
AN - SCOPUS:0034425715
SN - 1061-4036
VL - 25
SP - 444
EP - 447
JO - Nature Genetics
JF - Nature Genetics
IS - 4
ER -