Oligonucleotide inhibition of IL2Rα mRNA transcription by promoter region collinear triplex formation in lymphocytes
Open Access
- 25 June 1991
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 19 (12) , 3435-3441
- https://doi.org/10.1093/nar/19.12.3435
Abstract
The promoter region of the IL2Rα gene 5′ flanking sequence contains enhancer elements crucial for binding nuclear factors which upregulate transcription following T lymphocyte activation. A 3′ exonuclease resistant ollgonucleotide (3′A-IL28p, terminated by a free amine group at Its 3′ end) was designed to bind to the IL2Rα promoter region from −273 to −246, forming a collinear triplex spanning the xB enhancer (−266 to −256) as well as most of the serum response element (CArG box, −251 to −244). The binding site specificity of this oligonucleotide was demonstrated in electrophoretic mobility shift assays and by inhibition of restriction endonuclease (Hinfl) cleavage within the segment of the target DNA predicted to form a triplex with the oligonucleotide. Intact normal lymphocytes, preincubated for 2h with 3′A-IL28p, accumulated less IL2Rα mRNA relative to other mRNAs (c-myc, β-actin, IL2Rβ, IL-6) for up to 12h after PHA stimulation, than did lymphocytes treated with a control oligomer of similar composition but different sequence. Nuclear run-on studies demonstrated that the rate of IL2Rα mRNA synthesis relative to c-myc and β-actin was also selectively diminished by treatment with 3′A-IL28p. These experiments suggest that transcription of individual genes can be selectively modulated in living cells by sequence specific collinear triplex formation in regulatory enhancer sequences.Keywords
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