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Triplex formation by the human Ha-ras promoter inhibits Sp1 binding and in vitro transcription
C Mayfield1, S Ebbinghaus, J Gee
1Bolden Laboratory, Department of Medicine, University of Alabama at Birmingham 35294-3300.
Abstract:
The central role of the ras oncogenes in the pathogenesis of a wide variety of human malignancies is well established. Toward developing specific transcriptional inhibitors of the human Ha-ras oncogene, we have designed oligonucleotides to target a region of the Ha-ras promoter (-8 to -28) which contains two of the three Sp1 binding sites essential for transcriptional activity. Gel mobility analysis and DNase I footprinting demonstrate that an oligonucleotide (HR21ap) forms a sequence-specific triple helix with its target site in an antiparallel orientation with respect to the purine-rich duplex strand through predominantly G*G:C triplets. Within the Ha-ras promoter, HR21ap binds exclusively to the proximal target Sp1 sites over a similar nontarget distal sequence which, like the target, contains a consensus Sp1 site. Protein binding assays demonstrate that triplex formation by HR21ap inhibits Sp1 binding to the Ha-ras promoter. Moreover, oligonucleotide-directed triplex formation arrests Ha-ras promoter-dependent transcription in vitro. The results presented here suggest that triplex formation by the Ha-ras promoter targeted oligonucleotide may provide a means to specifically inhibit transcription of this oncogene in vivo.
Insights
Researchers designed a DNA molecule to block the Ha-ras oncogene. This molecule, HR21ap, forms a triple helix, inhibiting Sp1 binding and halting cancer gene transcription, offering a potential therapy for malignancies.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Ras oncogenes are crucial in human cancer development.
- Targeting oncogene transcription is a key strategy for cancer therapy.
Purpose of the Study:
- To develop specific transcriptional inhibitors for the human Ha-ras oncogene.
- To investigate the potential of triple helix-forming oligonucleotides for cancer gene inhibition.
Main Methods:
- Design of a triple helix-forming oligonucleotide (HR21ap) targeting the Ha-ras promoter.
- Gel mobility shift assays and DNase I footprinting to analyze HR21ap binding.
- Sp1 protein binding assays and in vitro transcription assays to assess functional inhibition.
Main Results:
- HR21ap forms a sequence-specific triple helix at the Ha-ras promoter's Sp1 binding sites.
- HR21ap selectively binds to target sites and inhibits Sp1 protein binding.
- Oligonucleotide-directed triplex formation effectively arrests Ha-ras promoter-dependent transcription in vitro.
Conclusions:
- Triple helix formation by HR21ap specifically inhibits Ha-ras oncogene transcription.
- This approach shows promise for developing novel therapeutic strategies against ras-driven cancers.