Regulated Expression of Transgenes in Embryonic Stem Cell-Derived Neural Cells

被引:2
作者
Lorberbaum, David S. [1 ]
Gottlieb, David [1 ]
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
关键词
nervous system; gene transcription; neural development; cis-regulatory element; gene promoter; ES cells; SPECIFIES GENE-EXPRESSION; RADIAL GLIA; RETINOIC ACID; MOTOR-NEURONS; SPINAL-CORD; IN-VITRO; DIFFERENTIATION; TRANSCRIPTION; ENHANCER; HB9;
D O I
10.1002/dvg.20696
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Discovery and characterization of gene promoters, enhancers and repressor binding elements is an important research area in neuroscience. Here, the suitability of embryonic stem cells and their neural derivatives as a model system for this research is investigated. Three neural transgenic constructs (from the Mnx1, Fabp7, and tuba1a genes) that have been validated in transgenic mice were inserted into embryonic stem cells as stable transgenes. These transgenic embryonic stem cells were differentiated into neural cultures and the pattern of transgene expression across a series of inducing conditions determined. The pattern of expression matched that predicted from transgenic mouse experiments for each of the three transgenes. The results show that embryonic stem cells and their neural derivatives comprise a promising model for investigating the mechanisms that control cell- and temporal-specific neural gene transcription. genesis 49:66-74,2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:66 / 74
页数:9
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