The long term goal of the proposal is to identify and purify the proteins involved in the replication of chloroplast DNA (ctDNA) followed by studying in vitro replication using purified proteins. Replication of ctDNA proceeds by the D-loop mechanism and involves both replicative intermediates produced by Cairn's mode of replication and rolling circle mechanism. We have mapped the origins of replication on the restriction endonuclease map of the pea ctDNA by electron microscopy. We have also developed a crude replication system that contains about 30 polypeptides and shows maximum DNA synthesis with recombinants pCP 12-7 and pCB 1-12 that have been found to contain the two D-loops. We now propose to progressively subclone these ctDNA fragments to eventually obtain the minimal ctDNA sequences that can replicate in an in vitro replication system. The exact sequences of the origins will be identified by obtaining deletion mutants followed by base substitution experiments. The D-loop DNA from supercoiled ctDNA will be analyzed for precisely mapping the initiation sites of replication and for the presence or absence of ribonucleotides as primers. We have obtained a pure preparation of topoisomerase I from the replication complex, and now plan to study its role in initiation of replication. We have obtained four DNA binding proteins whose role(s) in replication will also be studied. Experiments are proposed to find out whether a specific DNA primase or the chloroplast RNA polymerase serves to prime the initiation of replication. The replication of D-loop containing plasmids in vitro will be studied using pure DNA polymerase, topoisomerase I priming enzyme, DNA binding proteins, and any as yet unidentified proteins that are needed in the replication of ctDNA.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033725-05
Application #
3283674
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1984-09-01
Project End
1992-11-30
Budget Start
1988-12-01
Budget End
1989-11-30
Support Year
5
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Type
Schools of Arts and Sciences
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Nielsen, B L; Lu, Z; Tewari, K K (1993) Characterization of the pea chloroplast DNA OriA region. Plasmid 30:197-211
Nielsen, B L; Rajasekhar, V K; Tewari, K K (1991) Pea chloroplast DNA primase: characterization and role in initiation of replication. Plant Mol Biol 16:1019-34
Meeker, R; Nielsen, B; Tewari, K K (1988) Localization of replication origins in pea chloroplast DNA. Mol Cell Biol 8:1216-23
Gold, B; Carrillo, N; Tewari, K K et al. (1987) Nucleotide sequence of a preferred maize chloroplast genome template for in vitro DNA synthesis. Proc Natl Acad Sci U S A 84:194-8
Tewari, K K (1986) Purification and properties of chloroplast DNA polymerase. Methods Enzymol 118:186-201