New approaches for modelling sporadic genetic disease in the mouse

被引:12
作者
Fisher, Elizabeth M. C. [1 ]
Lana-Elola, Eva [2 ]
Watson, Sheona D. [2 ]
Vassiliou, George [3 ]
Tybulewicz, Victor L. J. [2 ]
机构
[1] UCL Inst Neurol, Dept Neurodegenerat Dis, London WC1N 3BG, England
[2] Natl Inst Med Res, MRC, London NW7 1AA, England
[3] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
SITE-SPECIFIC RECOMBINATION; INDUCED MITOTIC RECOMBINATION; CHIMERIC CRE RECOMBINASE; MCCUNE-ALBRIGHT SYNDROME; STIMULATORY G-PROTEIN; EMBRYONIC STEM-CELLS; SLEEPING-BEAUTY; MAMMALIAN-CELLS; TRANSGENIC MICE; MOSAIC ANALYSIS;
D O I
10.1242/dmm.001644
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sporadic diseases, which occur as single, scattered cases, are among the commonest causes of human morbidity and death. They result in a variety of diseases, including many cancers, premature aging, neurodegeneration and skeletal defects. They are often pathogenetically complex, involving a mosaic distribution of affected cells and are difficult to model in the mouse. Faithful models of sporadic diseases require innovative forms of genetic manipulation to accurately recreate their initiation and pathogenesis. Such modelling is crucial to understanding these diseases and, by extension, to the development of therapeutic approaches to treat them. This article focuses on sporadic diseases with a genetic aetiology, the challenges they pose to biomedical researchers, and the different current and developing approaches used to model such disorders in the mouse.
引用
收藏
页码:446 / 453
页数:8
相关论文
共 86 条
[31]   THE ROLE OF THE LOXP SPACER REGION IN P1 SITE-SPECIFIC RECOMBINATION [J].
HOESS, RH ;
WIERZBICKI, A ;
ABREMSKI, K .
NUCLEIC ACIDS RESEARCH, 1986, 14 (05) :2287-2300
[32]   Reversibility of acute B-cell leukaemia induced by BCR-ABL1 [J].
Huettner, CS ;
Zhang, P ;
Van Etten, RA ;
Tenen, DG .
NATURE GENETICS, 2000, 24 (01) :57-60
[33]   Molecular reconstruction of Sleeping beauty, a Tc1-like transposon from fish, and its transposition in human cells [J].
Ivics, Z ;
Hackett, PB ;
Plasterk, RH ;
Izsvak, Z .
CELL, 1997, 91 (04) :501-510
[34]   Sleeping Beauty, a wide host-range transposon vector for genetic transformation in vertebrates [J].
Izsvák, Z ;
Ivics, Z ;
Plasterk, RH .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 302 (01) :93-102
[35]   Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras [J].
Jackson, EL ;
Willis, N ;
Mercer, K ;
Bronson, RT ;
Crowley, D ;
Montoya, R ;
Jacks, T ;
Tuveson, DA .
GENES & DEVELOPMENT, 2001, 15 (24) :3243-3248
[36]   Mitochondrial DNA mutations and aging: devils in the details? [J].
Khrapko, Konstantin ;
Vijg, Jan .
TRENDS IN GENETICS, 2009, 25 (02) :91-98
[37]   Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice [J].
Kistner, A ;
Gossen, M ;
Zimmermann, F ;
Jerecic, J ;
Ullmer, C ;
Lubbert, H ;
Bujard, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :10933-10938
[38]   INDUCIBLE GENE TARGETING IN MICE [J].
KUHN, R ;
SCHWENK, F ;
AGUET, M ;
RAJEWSKY, K .
SCIENCE, 1995, 269 (5229) :1427-1429
[39]   Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging [J].
Kujoth, GC ;
Hiona, A ;
Pugh, TD ;
Someya, S ;
Panzer, K ;
Wohlgemuth, SE ;
Hofer, T ;
Seo, AY ;
Sullivan, R ;
Jobling, WA ;
Morrow, JD ;
Van Remmen, H ;
Sedivy, JM ;
Yamasoba, T ;
Tanokura, M ;
Weindruch, R ;
Leeuwenburgh, C ;
Prolla, TA .
SCIENCE, 2005, 309 (5733) :481-484
[40]   TARGETED ONCOGENE ACTIVATION BY SITE-SPECIFIC RECOMBINATION IN TRANSGENIC MICE [J].
LAKSO, M ;
SAUER, B ;
MOSINGER, B ;
LEE, EJ ;
MANNING, RW ;
YU, SH ;
MULDER, KL ;
WESTPHAL, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6232-6236