Replication of bacteriophage M13. XV. Location of the specific nick in M13 replicative form II accumulated in Escherichia coli polAex1

Author:

Nomura N,Ray D S

Abstract

M13 replicative form II (RFII) DNA was prepared from Escherichia coli RS5052 (polAex1) cells in the late stage of infection, and the DNA sequence at the discontinuity was examined. The data presented here suggest that the single discontinuity in the late stage of infection RFII maps at the same position as the gene II protein nicking site on fd RFI which was determined in vitro (Meyer et al., Nature (London) 278:365-367, 1979) and has a 5' terminal nucleotide sequence identical to that at the nick produced by gene II protein in vitro. The discontinuity in the in vivo RFII appears to be a single break in the phosphodiester backbone, leaving a 3' OH terminus. RFII molecules containing a gap, i.e., missing nucleotides at the site of discontinuity, were not detected.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference24 articles.

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3. Chromatography of 32P-labeled oligonucleotides on thin layers of DEAEcellulose;Brownlee G. G.;Eur. J. Biochem.,1969

4. Replication of bacteriophage M13. X. M13 replication in a mutant of Escherichia coli defective in the 5' -. 3' exonuclease associated with DNA polymerase I;Chen T.;J. Mol. Biol.,1976

5. Replication of bacteriophage M13. XIV. Differential inhibition of the replication of M13 and M13 miniphage in a mutant of Escherichia coli defective in the 5' -* 3' exonuclease associated with DNA polymerase I;Chen T.;J. Virol.,1978

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