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PMID: 6312322 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Viability of lambda phages carrying a perfect palindrome in the absence of recombination nucleases.

Nature ·Vol. 305 ·No. 5933 ·1983-00-00 ·Pages 448-51

Leach DR, Stahl FW

Abstract

In Escherichia coli in vitro constructions of perfect palindromes larger than 30 base pairs (bp) long have in general been unstable. A perfect palindrome has the unique possibility of forming a cruciform structure, and it is this feature which probably results in its instability. Negative supercoiling favours the formation of the cruciform conformation, which in turn causes the molecule to relax. This relaxation may render replicons containing large perfect palindromes inviable. An alternative hypothesis for inviability has been that the cruciform interferes with replication by favouring strand switching by polymerase I. Here we show that the simultaneous absence of two recombination nucleases, the recBC product, exonuclease V, and the sbcB product, exonuclease I, confers viability on a derivative of phage lambda carrying a perfect palindrome of inverted repeat length 1,600 bases. This observation suggests a third hypothesis--that nucleolytic cleavage of the cruciform is responsible for the inviability of the phage. Such an activity has been shown in vitro for T4 exonuclease VII.

MeSH Terms
Bacteriophage lambda/genetics Base Sequence DNA, Viral/genetics Escherichia coli Proteins Exodeoxyribonuclease V Exodeoxyribonucleases/physiology Exonucleases/physiology Hydrogen Bonding Nucleic Acid Conformation Recombination, Genetic
Chemicals
DNA, Viral Escherichia coli Proteins Exodeoxyribonucleases Exonucleases Exodeoxyribonuclease V exodeoxyribonuclease V, E coli
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Leach D R
Stahl F W
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1983-00-00
Pages
448-51
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NIGMS NIH HHS · GM 28369 · United States
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