Englander E W, Wolffe A P, Howard B H
Laboratory of Molecular Growth Regulation, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1993 Sep 15;268(26):19565-73.
Alu interspersed repetitive elements possess internal RNA polymerase III promoters which are strongly transcribed in vitro, yet these elements are nearly silent in somatic cells. To examine whether repression by chromatin proteins could contribute to the low level of Alu expression, a conserved Alu element from the fourth intron of the human alpha-fetoprotein gene was reconstituted with purified octamer or tetramer particles. Analysis of reconstitutes revealed that this Alu element directed translational and rotational positioning of octamers as well as tetramers. In vitro transcription experiments with reconstituted templates demonstrated that RNA polymerase III-dependent transcription of the Alu element was profoundly repressed by positioned octamer particles. Furthermore, complete CpG methylation of this template enhanced the capacity of tetramers to repress transcription.
Alu散布重复元件具有内部RNA聚合酶III启动子,这些启动子在体外能被强烈转录,但这些元件在体细胞中几乎不表达。为了研究染色质蛋白的抑制作用是否会导致Alu低水平表达,从人甲胎蛋白基因的第四个内含子中提取了一个保守的Alu元件,并用纯化的八聚体或四聚体颗粒进行重组。对重组体的分析表明,该Alu元件指导八聚体和四聚体的平移和旋转定位。用重组模板进行的体外转录实验表明,定位的八聚体颗粒能显著抑制Alu元件依赖RNA聚合酶III的转录。此外,该模板的完全CpG甲基化增强了四聚体抑制转录的能力。