Lim C S, Jabrane-Ferrat N, Fontes J D, Okamoto H, Garovoy M R, Peterlin B M, Hunt C A
Department of Biopharmaceutical Sciences, University of California, San Francisco, CA 94143-0446, USA.
Nucleic Acids Res. 1997 Feb 1;25(3):575-81. doi: 10.1093/nar/25.3.575.
DNA dumbbells are stable, short segments of double-stranded DNA with closed nucleotide loops on each end, conferring resistance to exonucleases. Dumbbells may be designed to interact with transcription factors in a sequence-specific manner. The internal based paired sequence of DNA dumbbells in this study contains the X-box, a positive regulatory motif found in all MHC class II DRA promoters. In electrophoretic mobility shift assays (EMSAs), dumbbells and other oligonucleotides ('decoys') with the core X-box sequence were found to compete with the native strand for binding to X-box binding proteins (including RFX1). However, only the X-box dumbbell was capable of forming detectable complexes with such proteins using EMSA. In a model cell system, dumbbells were tested for their ability to block RFX1VP16 activation of a plasmid containing multiple repeats of the X-box linked to the CAT gene. While it appeared that dumbbells could block this activation, the effect was non-specific. This and further evidence suggests an inhibition of transcription, most likely via an interaction with the general transcriptional machinery.
DNA哑铃是稳定的双链DNA短片段,两端带有封闭的核苷酸环,赋予其对外切核酸酶的抗性。哑铃可设计成以序列特异性方式与转录因子相互作用。本研究中DNA哑铃的内部碱基配对序列包含X盒,这是在所有MHC II类DRA启动子中发现的一个正向调控基序。在电泳迁移率变动分析(EMSA)中,发现带有核心X盒序列的哑铃和其他寡核苷酸(“诱饵”)与天然链竞争结合X盒结合蛋白(包括RFX1)。然而,只有X盒哑铃能够使用EMSA与这类蛋白形成可检测到的复合物。在一个模型细胞系统中,测试了哑铃阻断RFX1VP16对含有与CAT基因相连的多个X盒重复序列的质粒激活的能力。虽然看起来哑铃可以阻断这种激活,但这种效应是非特异性的。这一现象及进一步的证据表明存在转录抑制,最有可能是通过与通用转录机制的相互作用实现的。