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Title: Repair of mismatched basepairs in mammalian DNA. Progress report, March 1, 1990--February 28, 1991

Technical Report ·
DOI:https://doi.org/10.2172/10146510· OSTI ID:10146510

We have concentrated on three specific areas of our research plan. Our greatest emphasis is on the role of single strand nicks in influencing template strand selection in mismatch repair. We have found, that the ability of a nick in one strand to influence which strand is repaired is not a simple function of distance from the mismatched site but rather that an hot spot where a nick is more likely to have an influence can exist. The second line was production of single-genotype heteroduplexes in order to examine independently the repair of T/G and A/C mispairs within the same sequence context as in our mixed mispair preparations. We have shown preparations of supercoiled heteroduplex can be prepared that were exclusively T/G or exclusively A/C at the mispair site. The third effort has been to understand the difference in repair bias of different cell lines or different transfection conditions as it may relate to different repair systems in the cell. We have identified some of the sources of variation, including cell cycle position. We hope to continue this work to more precisely identify the phase of the cell cycle.

Research Organization:
Florida State Univ., Tallahassee, FL (United States). Inst. of Molecular Biophysics
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
FG05-87ER60545
OSTI ID:
10146510
Report Number(s):
DOE/ER/60545-4; ON: DE93013262
Resource Relation:
Other Information: PBD: Aug 1991
Country of Publication:
United States
Language:
English