The ability of DNA to form triple helices between duplex DNA and single strands of appropriate sequence offers promise as a developing technique for sequence-specific DNA cleavage and the modulation of gene expression, including therapeutic uses. The major limitation of this approach has been that triplex formation only occurs at sequences that are largely or entirely homopurine tracts. The proposed research will investigate new approaches for the loosening of this requirement, with the ultimate goal being the capability to achieve triplex formation at any sequence. One new approach involves the pairing of a single strand with both strands of a mixed sequence duplex, with Py.PuPy base triplets being formed when purines are on one strand of the Watson-Crick duplex and Pu.PuPy triplets when that are on the other strand. This approach maintains the required polarity for both pairing motifs without requiring any unusual linkages or base analogs. Preliminary studies on intramolecular triplex formation have demonstrated the promise of this strategy for PuPuPuPuPyPyPyPy sequences. The proposed research will examine to what extent this strand-switching approach can obviate the need for homopurine sequences. A pool of single-stranded DNA molecules of random sequence (up to 1010- 1012 different sequences) will also be screened to select the best sequences for triplex formation with mixed sequence targets of various types. Triplex formation will be employed to control gene expression at the DNA and RNA level in the human immunodeficiency virus (HIV-1). A novel approach based on triplex formation (triplex-mediated antisense) is proposed for arresting gene expression at the RNA level.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM048863-02
Application #
2186374
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1993-05-01
Project End
1997-04-30
Budget Start
1994-05-01
Budget End
1995-04-30
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Sri International
Department
Type
DUNS #
City
Menlo Park
State
CA
Country
United States
Zip Code
94025
Belotserkovskii, B P; Johnston, B H (1997) A random-walk model for retardation of interacting species during gel electrophoresis: implications for gel-shift assays. Biophys J 73:1288-98
Belotserkovskii, B P; Johnston, B H (1997) Denaturation and association of DNA sequences by certain polypropylene surfaces. Anal Biochem 251:251-62
Balatskaya, S V; Belotserkovskii, B P; Johnston, B H (1996) Alternate-strand triplex formation: modulation of binding to matched and mismatched duplexes by sequence choice in the Pu-Pu-Py block. Biochemistry 35:13328-37
Belotserkovskii, B P; Johnston, B H (1996) Capture in the gel: intermoleculare triplex formation during gel electrophoresis. Electrophoresis 17:1528-34