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Title: Repair of damaged DNA in-vivo. Comprehensive progress report, August 1980-August 1983

Technical Report ·
OSTI ID:5213215

We have extended our characterization of long patch excision repair (LPER) and have demonstrated that LPER is not mutagenic (or error-prone); that the recA function is required for LPER, at least for its regulation; that the substrate for LPER is produced as a linear (not an exponential) function of uv (254 nm) dose; and that LPER can occur in uvr/sup -/ cells treated with N-methyl-N-nitro-N-nitrosoguanidine (MNNG). We have developed 3 methods for measuring the frequency of interstrand crosslinks in DNA and are now applying these methods to the study of the formation and repair of DNA crosslinks in E.Coli. We have developed a monoclonal antibody specific for thymine glycol in DNA, and are using it to study the repair of thymine glycol in E. coli.

Research Organization:
Stanford Univ., CA (USA)
DOE Contract Number:
AT03-76EV70007
OSTI ID:
5213215
Report Number(s):
DOE/EV/70007-T1; ON: DE84006020
Country of Publication:
United States
Language:
English

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