Contemporary approaches for modifying the mouse genome

被引:27
作者
Adams, David J. [1 ]
van der Weyden, Louise [1 ]
机构
[1] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
基金
英国惠康基金;
关键词
gene targeting; transposons; mutagenesis; embryonic stem cells;
D O I
10.1152/physiolgenomics.90242.2008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adams DJ, van der Weyden L. Contemporary approaches for modifying the mouse genome. Physiol Genomics 34: 225-238, 2008. First published June 17, 2008; doi:10.1152/physiolgenomics.90242.2008.-The mouse is a premiere experimental organism that has contributed significantly to our understanding of vertebrate biology. Manipulation of the mouse genome via embryonic stem (ES) cell technology makes it possible to engineer an almost limitless repertoire of mutations to model human disease and assess gene function. In this review we outline recent advances in mouse experimental genetics and provide a "how-to" guide for those people wishing to access this technology. We also discuss new technologies, such as transposon-mediated mutagenesis, and resources of targeting vectors and ES cells, which are likely to dramatically accelerate the pace with which we can assess gene function in vivo, and the progress of forward and reverse genetic screens in mice.
引用
收藏
页码:225 / 238
页数:14
相关论文
共 88 条
[41]   Transgenic RNA interference in ES cell-derived embryos recapitulates a genetic null phenotype [J].
Kunath, T ;
Gish, G ;
Lickert, H ;
Jones, N ;
Pawson, T ;
Rossant, J .
NATURE BIOTECHNOLOGY, 2003, 21 (05) :559-561
[42]   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
[43]   A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA [J].
Lee, EC ;
Yu, DG ;
de Velasco, JM ;
Tessarollo, L ;
Swing, DA ;
Court, DL ;
Jenkins, NA ;
Copeland, NG .
GENOMICS, 2001, 73 (01) :56-65
[44]   TARGETED MUTATION OF THE DNA METHYLTRANSFERASE GENE RESULTS IN EMBRYONIC LETHALITY [J].
LI, E ;
BESTOR, TH ;
JAENISCH, R .
CELL, 1992, 69 (06) :915-926
[45]   Chromosomal transposition of a Tc1/mariner-like element in mouse embryonic stem cells [J].
Luo, GB ;
Ivics, Z ;
Izsvák, Z ;
Bradley, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10769-10773
[46]   ISOLATION OF A PLURIPOTENT CELL-LINE FROM EARLY MOUSE EMBRYOS CULTURED IN MEDIUM CONDITIONED BY TERATOCARCINOMA STEM-CELLS [J].
MARTIN, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (12) :7634-7638
[47]  
McClive P, 1998, DEV DYNAM, V212, P267, DOI 10.1002/(SICI)1097-0177(199806)212:2<267::AID-AJA11>3.0.CO
[48]  
2-1
[49]   IDENTIFICATION OF THE CROSSOVER SITE DURING FLP-MEDIATED RECOMBINATION IN THE SACCHAROMYCES-CEREVISIAE PLASMID 2-MU-M CIRCLE [J].
MCLEOD, M ;
CRAFT, S ;
BROACH, JR .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (10) :3357-3367
[50]   A conserved transcriptional enhancer that specifies Tyrp1 expression to melanocytes [J].
Murisier, Fabien ;
Guichard, Sabrina ;
Beermann, Friedrich .
DEVELOPMENTAL BIOLOGY, 2006, 298 (02) :644-655