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Evidence That Dimers Remaining in Preinduced Escherichia Coli B/r Hcr+ Become Insensitive After DNA Replication to the Extract from Micrococcus Luteus

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1981 Nov 1
PMID 7030422
Citations 2
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Abstract

In Escherichia coli B/r Her+ irradiated with two separate fluences, dimer excision is prematurely interrupted. The present study was designed to follow tha fate of dimers remaining unexcised. The results imply that these dimers (or distortions containing dimers) are transformed on replication from the state of sensitivity to the state of insensitivity to endonuclease from Micrococcus luteus. This conclusion is based on the following findings: (a) dimers were radiochromatographically detectable in DNA replicated after UV, which indicated that they were tolerated on replication. (b) Similar amounts of dimers were detected radiochromatographically both in DNA remaining unreplicated and DNA twice replicated after UV, This along with the low transfer of parental label into daughter DNA, indicated that dimers remained in situ in parental chains. (c) Immediately after UV, all parental DNA contained numerous sites sensitive to the extract from M. luteus. 2 h after UV, a portion of parental DNA still contained a number of endonuclease-sensitive (Es) sites, while another portion of parental DNA and all daughter DNA were free of Es sites. (d) The occurrence of parental DNA free of Es sites was not temporally correlated with dimer excision, but with the first round of DNA replication. (e) The amount of DNA free of Es sites corresponded to the amount of replicated DNA. (f) Separation of replicated and unreplicated DNA, and detection of Es sites in both portions separately showed that the replicated DNA was almost free of Es sites, whereas unreplicated DNA contained a number of such sites.

Citing Articles

Replication of UV-irradiated single-stranded DNA by DNA polymerase III holoenzyme of Escherichia coli: evidence for bypass of pyrimidine photodimers.

Livneh Z Proc Natl Acad Sci U S A. 1986; 83(13):4599-603.

PMID: 2941756 PMC: 323788. DOI: 10.1073/pnas.83.13.4599.


Translesion synthesis is the main component of SOS repair in bacteriophage lambda DNA.

Defais M, Lesca C, Monsarrat B, Hanawalt P J Bacteriol. 1989; 171(9):4938-44.

PMID: 2527845 PMC: 210300. DOI: 10.1128/jb.171.9.4938-4944.1989.

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