Quiet mutations in inbred strains of mice

被引:56
作者
Stevens, James C. [1 ]
Banks, Gareth T. [1 ]
Festing, Michael F. W. [2 ]
Fisher, Elizabeth M. C. [1 ]
机构
[1] Inst Neurol, Univ Coll London, Neurol Inst, Dept Neurodegenerat Dis, London WC1N 3BG, England
[2] The NC3Rs, London W1B 1AL, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/j.molmed.2007.10.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The year 2009 is the 100th anniversary of the founding of the first inbred strain of mouse, called DBA. During the last 100 years, inbred strains have proved their value for biomedical research and the number of such strains has mushroomed to over 450, each with different genotypic and phenotypic characteristics and useful for the study of disease and normal function. However, although inbred strains are stable, they are not fixed entities and researchers need to be aware of the phenomena of new mutations and of genetic drift, which occur within all mouse colonies. If the mutations are what we term in this review 'quiet mutations', then they might result in rather unexpected and sometimes tremendously valuable results. Here, we discuss these phenomena and look at how new genomic technologies might help us to detect 'quiet mutations' and use them to our advantage.
引用
收藏
页码:512 / 519
页数:8
相关论文
共 60 条
[1]   E3 ubiquitin ligase Cblb regulates the acute inflammatory response underlying lung injury [J].
Bachmaier, Kurt ;
Toya, Sophie ;
Gao, Xiaopei ;
Triantafillou, Thomas ;
Garrean, Sean ;
Park, Gye Young ;
Frey, Randall S. ;
Vogel, Stephen ;
Minshall, Richard ;
Christman, John W. ;
Tiruppathi, Chinnaswamy ;
Malik, Asrar B. .
NATURE MEDICINE, 2007, 13 (08) :920-926
[2]  
BAILEY DONALD W., 1959, JOUR HEREDITY, V50, P26
[3]   Genealogies of mouse inbred strains [J].
Beck, JA ;
Lloyd, S ;
Hafezparast, M ;
Lennon-Pierce, M ;
Eppig, JT ;
Festing, MFW ;
Fisher, EMC .
NATURE GENETICS, 2000, 24 (01) :23-+
[4]   Whole-genome re-sequencing [J].
Bentley, David R. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2006, 16 (06) :545-552
[5]   Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project [J].
Birney, Ewan ;
Stamatoyannopoulos, John A. ;
Dutta, Anindya ;
Guigo, Roderic ;
Gingeras, Thomas R. ;
Margulies, Elliott H. ;
Weng, Zhiping ;
Snyder, Michael ;
Dermitzakis, Emmanouil T. ;
Stamatoyannopoulos, John A. ;
Thurman, Robert E. ;
Kuehn, Michael S. ;
Taylor, Christopher M. ;
Neph, Shane ;
Koch, Christoph M. ;
Asthana, Saurabh ;
Malhotra, Ankit ;
Adzhubei, Ivan ;
Greenbaum, Jason A. ;
Andrews, Robert M. ;
Flicek, Paul ;
Boyle, Patrick J. ;
Cao, Hua ;
Carter, Nigel P. ;
Clelland, Gayle K. ;
Davis, Sean ;
Day, Nathan ;
Dhami, Pawandeep ;
Dillon, Shane C. ;
Dorschner, Michael O. ;
Fiegler, Heike ;
Giresi, Paul G. ;
Goldy, Jeff ;
Hawrylycz, Michael ;
Haydock, Andrew ;
Humbert, Richard ;
James, Keith D. ;
Johnson, Brett E. ;
Johnson, Ericka M. ;
Frum, Tristan T. ;
Rosenzweig, Elizabeth R. ;
Karnani, Neerja ;
Lee, Kirsten ;
Lefebvre, Gregory C. ;
Navas, Patrick A. ;
Neri, Fidencio ;
Parker, Stephen C. J. ;
Sabo, Peter J. ;
Sandstrom, Richard ;
Shafer, Anthony .
NATURE, 2007, 447 (7146) :799-816
[6]   Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B [J].
Bittner, RE ;
Anderson, LVB ;
Burkhardt, E ;
Bashir, R ;
Vafiadaki, E ;
Ivanova, S ;
Raffelsberger, T ;
Maerk, I ;
Höger, H ;
Jung, M ;
Karbasiyan, M ;
Storch, M ;
Lassmann, H ;
Moss, JA ;
Davison, K ;
Harrison, R ;
Bushby, KMD ;
Reis, A .
NATURE GENETICS, 1999, 23 (02) :141-142
[7]   X-CHROMOSOME-LINKED MUSCULAR-DYSTROPHY (MDX) IN THE MOUSE [J].
BULFIELD, G ;
SILLER, WG ;
WIGHT, PAL ;
MOORE, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1189-1192
[8]   Improved generation of C57BL/6J mouse embryonic stem cells in a defined serum-free media [J].
Cheng, J ;
Dutra, A ;
Takesono, A ;
Garrett-Beal, L ;
Schwartzberg, PL .
GENESIS, 2004, 39 (02) :100-104
[9]   The origins and uses of mouse outbred stocks [J].
Chia, R ;
Achilli, F ;
Festing, MFW ;
Fisher, EMC .
NATURE GENETICS, 2005, 37 (11) :1181-1186
[10]   Molecular definition of an allelic series of mutations disrupting the mouse Lmx1a (dreher) gene [J].
Chizhikov, Victor ;
Steshina, Ekaterina ;
Roberts, Richard ;
Ilkin, Yesim ;
Washburn, Linda ;
Millen, Kathleen J. .
MAMMALIAN GENOME, 2006, 17 (10) :1025-1032