Li H L, Kmiec E B
Department of Biochemistry and Biophysics, University of California, Davis 95616.
Mol Endocrinol. 1990 Aug;4(8):1173-82. doi: 10.1210/mend-4-8-1173.
In vitro transcription experiments using a Xenopus laevis cell-free extract have demonstrated that a DNA fragment containing a glucocorticoid response element (GRE) significantly enhances the expression of a methionine tRNA gene. This stimulation can be observed when the element is located in cis or trans. In the cis configuration, the element can be located 2900 basepairs from the gene and still display transcriptional enhancement. In trans, the enhancement can occur at a low element to template molecular ratio. The nucleosome positioning and chromatin structure near the tRNA gene appear to be unaffected by the presence of the long terminal repeat of the mouse mammary tumor virus which contains the GRE. Taken together, these data suggest that GREs can stimulate transcription of hormonally unresponsive genes, perhaps by providing a "molecular sink" to which inhibitors may bind. Further experimentation may reveal a correlation between these in vitro studies and in vivo gene regulation.
使用非洲爪蟾无细胞提取物进行的体外转录实验表明,包含糖皮质激素反应元件(GRE)的DNA片段可显著增强甲硫氨酸tRNA基因的表达。当该元件位于顺式或反式时均可观察到这种刺激作用。在顺式构型中,该元件可位于距基因2900个碱基对处,仍表现出转录增强作用。在反式情况下,在元件与模板分子比例较低时也可发生增强作用。tRNA基因附近的核小体定位和染色质结构似乎不受含有GRE的小鼠乳腺肿瘤病毒长末端重复序列存在的影响。综合来看,这些数据表明GRE可能通过提供一个抑制剂可能结合的“分子陷阱”来刺激激素无反应基因的转录。进一步的实验可能会揭示这些体外研究与体内基因调控之间的相关性。