Sequence-independent inhibition of RNA transcription by DNA dumbbells and other decoys
Author(s) -
Carol S. Lim,
Nabila JabraneFerrat,
Joseph D. Fontes,
Hiroshi Okamoto,
Marvin R. Garovoy,
B. Matija Peterlin,
C. Anthony Hunt
Publication year - 1997
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/25.3.575
Subject(s) - biology , dna , transcription (linguistics) , electrophoretic mobility shift assay , promoter , oligonucleotide , transcription factor , decoy , microbiology and biotechnology , genetics , dna binding protein , rna , base pair , gene , gene expression , philosophy , linguistics , receptor
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.
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