Department of Pediatrics, University of Cincinnati, Howard Hughes Medical Institute, Cincinnati Children's Hospital Medical Center, 240 Albert Sabin Way, S4.409, Cincinnati, OH 45229, USA.
Circ Res. 2012 Aug 31;111(6):761-77. doi: 10.1161/CIRCRESAHA.111.262717.
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.
在过去的 20 年中,现代小鼠遗传学的出现使许多基于疾病的研究领域受益,也许没有哪个领域比心脏生物学受益更深。事实上,鉴于越来越多的分子试剂/启动子和“促进剂”小鼠系的出现,心脏现在可以说是最容易进行基因操作的组织之一。现在可以随时在小鼠心脏中修饰基本上任何基因或部分基因产物的表达,无论是获得功能还是丧失功能。本综述旨在为非小鼠遗传学家和/或初级研究人员提供一本手册,以便成功地在心脏中操纵任何基因或 RNA 产物,同时避免假象。在本综述中,提出了指导方针、陷阱和限制,以便能够对心脏基因型-表型关系进行严格和适当的检查。本综述使用该领域的示例来说明在使用基因修饰小鼠模型研究心脏生物学时必须考虑的广泛的实验和设计细节。