Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Cell and Neurobiology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Curr Opin Nephrol Hypertens. 2011 Jul;20(4):391-9. doi: 10.1097/MNH.0b013e328347768a.
Several advances have been made to manipulate the rat genome in the last 2 years. This review aims to describe these advances in rat genetic manipulations, with an emphasis on their current status and their prospects and applications in the postgenomic era.
Authentic rat embryonic stem cells were derived in 2008 using the 2i/3i culture system. This led to the generation of the first gene knockout rats via embryonic stem cell-based gene targeting. The development of zinc-finger nucleases (ZFNs) provided an alternative approach that avoids the necessity of germline competent embryonic stem cells. Meanwhile, improvements have been made to the well established random mutagenesis mediated by transposons or N-ethyl-N-nitrosourea (ENU). The in-vitro rat spermatogonial stem cell (SSC) system has greatly optimized these phenotype-driven approaches for future applications.
The rat has long been a prime model organism in physiological, pharmacological and neurobehavioral studies. The recent advances of rat reverse genetic approaches, together with the classical ENU and transposon mutagenesis system, will contribute tremendously to the deciphering of gene functions and the creation of rat disease models.
在过去的两年中,人们在操纵大鼠基因组方面取得了多项进展。本综述旨在描述大鼠遗传操作方面的这些进展,重点介绍其当前状况及其在后基因组时代的前景和应用。
2008 年,使用 2i/3i 培养系统成功获得了真正的大鼠胚胎干细胞。这导致了首次通过基于胚胎干细胞的基因靶向产生基因敲除大鼠。锌指核酸酶 (ZFNs) 的发展提供了一种替代方法,避免了对生殖系胚胎干细胞的必要性。同时,对转座子或 N-乙基-N-亚硝脲 (ENU) 介导的随机诱变进行了改进。体外大鼠精原干细胞 (SSC) 系统极大地优化了这些表型驱动的方法,以用于未来的应用。
大鼠长期以来一直是生理、药理学和神经行为学研究的主要模式生物。大鼠反向遗传方法的最新进展,以及经典的ENU 和转座子诱变系统,将极大地促进基因功能的破译和大鼠疾病模型的创建。