This proposal is directed towards our understanding of the functions and mechanisms of multiple DNA topoisomerases in eukaryotic cells. Eukaryotic DNA topoisomerase I breaks and rejoins one DNA strand at a time whereas eukaryotic DNA topoisoemrase II breaks and rejoins both DNA strands in concert. Both enzymes may be involved in controlling the complex topological state of DNA. We will investigate how these enzymes control the topological structure of DNA and how these enzymes affect various genetic processes. (1) We will study the roles of DNA topoisomerases in eukaryotic gene expression using both the Drosophila heat shock system and simian virus 40(SV40) system. (2) We will investigate the roles of DNA topoisomerases in SV40 DNA replication. We are particularly interested in the possibility that topo II may signal initiation of DNA replication by its putative gyrase activity. (3) We will try to isolate mutants of topoisomerases from Saccharomyces cerevisiae. In particular, we will use P4 knotted DNA as substrate to screen cdc mutants in vitro. (4) We will clone the human topoisomerase genes to study the protein sequence and transcriptional regulation. (5) We will study the regulation and modification of topoisomerases in cells using logical methods. (6) We will study the interactions of eukaryotic DNA topoisomerases with DNA, nucleosomes and chromosomal proteins. (7) We will investigate the possibility that DNA topoisomerases may be involved in DNA sequence rearrangement. The topoisomerase cleavage sites will be compared with the sequenced integration sites of SV40 DNA. The long-term objective of this project is to understand the functions and mechanisms of DNA topoisomerases in various genetic processes such as DNA replication, RNA transcription, recombination and nucleic acids rearrangements.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM027731-06
Application #
3274964
Study Section
Genetics Study Section (GEN)
Project Start
1980-04-01
Project End
1988-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Nur-E-Kamal, Alam; Li, Tsai-Kun; Zhang, Ailing et al. (2003) Single-stranded DNA induces ataxia telangiectasia mutant (ATM)/p53-dependent DNA damage and apoptotic signals. J Biol Chem 278:12475-81
Qi, Haiyan; Li, Tsai-Kun; Kuo, Debbie et al. (2003) Inactivation of Cdc13p triggers MEC1-dependent apoptotic signals in yeast. J Biol Chem 278:15136-41
Zhou, Nai; Xiao, Hai; Li, Tsai-Kun et al. (2003) DNA damage-mediated apoptosis induced by selenium compounds. J Biol Chem 278:29532-7
Xiao, Hai; Li, Tsai-Kun; Yang, Jin-Ming et al. (2003) Acidic pH induces topoisomerase II-mediated DNA damage. Proc Natl Acad Sci U S A 100:5205-10
Xiao, Hai; Mao, Yong; Desai, Shyamal D et al. (2003) The topoisomerase IIbeta circular clamp arrests transcription and signals a 26S proteasome pathway. Proc Natl Acad Sci U S A 100:3239-44
Mao, Y; Desai, S D; Ting, C Y et al. (2001) 26 S proteasome-mediated degradation of topoisomerase II cleavable complexes. J Biol Chem 276:40652-8
Wang, H; Mao, Y; Zhou, N et al. (2001) Atp-bound topoisomerase ii as a target for antitumor drugs. J Biol Chem 276:15990-5
Wang, H; Mao, Y; Chen, A Y et al. (2001) Stimulation of topoisomerase II-mediated DNA damage via a mechanism involving protein thiolation. Biochemistry 40:3316-23
Li, T K; Liu, L F (2001) Tumor cell death induced by topoisomerase-targeting drugs. Annu Rev Pharmacol Toxicol 41:53-77
Sim, S P; Liu, L F (2001) Nucleolytic cleavage of the mixed lineage leukemia breakpoint cluster region during apoptosis. J Biol Chem 276:31590-5

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