Accession Number : ADA191557
Title : Molecular Toxicology of Chromatin.
Descriptive Note : Annual progress rept. 1 Jan-31 Dec 87,
Corporate Author : CALIFORNIA UNIV SAN FRANCISCO CARDIOVASCULAR RESEARCH INST
Personal Author(s) : Kun, Ernest
PDF Url : ADA191557
Report Date : 31 Dec 1987
Pagination or Media Count : 149
Abstract : Part I. Benzamide-DNA Interactions; Deductions from Binding, Enzyme-Kinetics and from X-ray Structural Analysis of a 9-Ethyladenine-Benzamide Adduct: The interaction of benzamide with the isolated components of calf thymus poly(ADP-ribose) polymerase and with liver nuclei has been investigated. Part II. Molecular Interactions Between DNA, Poly(ADP-Ribose) Polymerase and Histones: Molecular interactions between purified poly(ADP-ribose) polymerase, whole thymus histones, histone H1, rat fibroblast genomic DNA, and closed circular and linearized SV40 DNA were determined by the nitrocellulose filter binding technique. Binding of the polymerase protein, or histones, to DNA was greatly augmented when both enzyme protein and histones were present simultaneously. Part III. Analysis of the Molecular Contacts Between Poly(ADP-ribose) Polymerase and DNA: The interaction between poly (ADP-ribose) polymerase and various uniquely end labeled restriction fragments from SV40 an pBR322 DNAs was studied employing nuclease protection experiments. DNasel footprinting indicated that approximately 66-85 bp of DNA was protected by poly (ADP-ribose) polymerase from DNasel attack, and that a segment of DNA probably lies outside on the surface of the polymerase protein in the polymerase-DNA complex.
Descriptors : *CHROMATIN, *ENZYMES, *TOXICOLOGY, *MOLECULAR BIOLOGY, ADHESION, AMIDES, BENZENE, DEOXYRIBONUCLEIC ACIDS, FILTERS, FRAGMENTS, HISTONES, INTERACTIONS, ISOLATION, LIVER, MOLECULE MOLECULE INTERACTIONS, MOLECULES, NITROCELLULOSE, NUCLEASE, NUCLEI, PROTECTION, PROTEINS, THYMUS, X RAYS, MOLECULAR STRUCTURE, ADENOSINE PHOSPHATES
Subject Categories : Toxicology
Genetic Engineering and Molecular Biology
Distribution Statement : APPROVED FOR PUBLIC RELEASE