Lost in Transgenesis A User's Guide for Genetically Manipulating the Mouse in Cardiac Research

被引:92
作者
Davis, Jennifer
Maillet, Marjorie
Miano, Joseph M. [2 ]
Molkentin, Jeffery D. [1 ]
机构
[1] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Howard Hughes Med Inst, Dept Pediat, Cincinnati, OH 45229 USA
[2] Univ Rochester, Sch Med & Dent, Aab Cardiovasc Res Inst, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
genetics; mouse heart development; transgene; transgenic mice; MYOSIN HEAVY-CHAIN; FAMILIAL HYPERTROPHIC CARDIOMYOPATHY; TRANSCRIPTION FACTOR MEF2C; HOMEOBOX GENE NKX2-5; SMOOTH-MUSCLE-CELLS; DELTA-NULL MICE; IN-VIVO; PRESSURE-OVERLOAD; ALPHA-MYOSIN; GERM-LINE;
D O I
10.1161/CIRCRESAHA.111.262717
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The advent of modern mouse genetics has benefited many fields of diseased-based research over the past 20 years, none perhaps more profoundly than cardiac biology. Indeed, the heart is now arguably one of the easiest tissues to genetically manipulate, given the availability of an ever-growing tool chest of molecular reagents/promoters and "facilitator" mouse lines. It is now possible to modify the expression of essentially any gene or partial gene product in the mouse heart at any time, either gain or loss of function. This review is designed as a handbook for the nonmouse geneticist and/or junior investigator to permit the successful manipulation of any gene or RNA product in the heart, while avoiding artifacts. In the present review, guidelines, pitfalls, and limitations are presented so that rigorous and appropriate examination of cardiac genotype-phenotype relationships can be performed. This review uses examples from the field to illustrate the vast spectrum of experimental and design details that must be considered when using genetically modified mouse models to study cardiac biology. (Circ Res. 2012;111:761-777.)
引用
收藏
页码:761 / +
页数:24
相关论文
共 131 条
[81]   A calcineurin-dependent transcriptional pathway for cardiac hypertrophy [J].
Molkentin, JD ;
Lu, JR ;
Antos, CL ;
Markham, B ;
Richardson, J ;
Robbins, J ;
Grant, SR ;
Olson, EN .
CELL, 1998, 93 (02) :215-228
[82]   REGULATION OF MYOSIN HEAVY-CHAIN GENES IN THE HEART [J].
MORKIN, E .
CIRCULATION, 1993, 87 (05) :1451-1460
[83]  
Moses Kelvin A., 2001, Genesis The Journal of Genetics and Development, V31, P176, DOI 10.1002/gene.10022
[84]   MOLECULAR-BASIS OF CARDIAC-PERFORMANCE - PLASTICITY OF THE MYOCARDIUM GENERATED THROUGH PROTEIN ISOFORM SWITCHES [J].
NADALGINARD, B ;
MAHDAVI, V .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) :1693-1700
[85]   FISH analysis of 142 EGFP transgene integration sites into the mouse genome [J].
Nakanishi, T ;
Kuroiwa, A ;
Yamada, S ;
Isotani, A ;
Yamashita, A ;
Tairaka, A ;
Hayashi, T ;
Takagi, T ;
Ikawa, M ;
Matsuda, Y ;
Okabe, M .
GENOMICS, 2002, 80 (06) :564-574
[86]   CARDIAC MYOSIN HEAVY-CHAIN MESSENGER-RNA EXPRESSION AND MYOCARDIAL-FUNCTION IN THE MOUSE HEART [J].
NG, WA ;
GRUPP, IL ;
SUBRAMANIAM, A ;
ROBBINS, J .
CIRCULATION RESEARCH, 1991, 68 (06) :1742-1750
[87]  
Novak A, 2000, GENESIS, V28, P147, DOI 10.1002/1526-968X(200011/12)28:3/4<147::AID-GENE90>3.0.CO
[88]  
2-G
[89]   POSITIONAL SPECIFICATION OF VENTRICULAR MYOSIN LIGHT CHAIN-2 EXPRESSION IN THE PRIMITIVE MURINE HEART TUBE [J].
OBRIEN, TX ;
LEE, KJ ;
CHIEN, KR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5157-5161
[90]  
OCHMAN H, 1988, GENETICS, V120, P621