Wight P A, Dobretsova A
Department of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, Ark. 72205, USA.
Dev Neurosci. 1998;20(6):552-8. doi: 10.1159/000017357.
Sequences from the first intron of the mouse myelin proteolipid protein (PLP) gene were examined for their ability to modulate PLP gene expression. Glial (N20.1) or nonglial (NIH 3T3) cells were transiently transfected with constructs that contained 1.4 kb of PLP promoter sequence driving luciferase reporter gene expression, as well as various portions of PLP intron 1 DNA. Although these same PLP intron 1 fragments enhanced reporter gene expression from a heterologous basal promoter in a previous study, the results reported here demonstrate that they do not augment PLP promoter activity. Thus, the regulation of PLP cell-type-specific expression, conferred by the first intron, appears to be mediated by an enhancer-independent mechanism.
对小鼠髓鞘蛋白脂蛋白(PLP)基因第一个内含子的序列进行了研究,以考察它们调节PLP基因表达的能力。用含有驱动荧光素酶报告基因表达的1.4 kb PLP启动子序列以及PLP内含子1 DNA不同片段的构建体瞬时转染胶质细胞(N20.1)或非胶质细胞(NIH 3T3)。尽管在先前的一项研究中,这些相同的PLP内含子1片段增强了来自异源基础启动子的报告基因表达,但此处报道的结果表明它们不会增强PLP启动子活性。因此,由第一个内含子赋予的PLP细胞类型特异性表达的调控似乎是由一种不依赖增强子的机制介导的。