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PMID: 6288263 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

DNA intermediates in transposition of phage Mu.

Cell ·Vol. 29 ·No. 2 ·1982-06-00 ·Pages 561-71

Harshey RM, McKay R, Bukhari AI

Abstract

Transposable genetic elements can insert into DNA sites that have no homology to themselves. Evidence that there is a physical linkage between a transposable element and its target DNA sequence during transposition comes from studies on bacteriophage Mu DNA transposition in which plasmids containing Mu DNA have been shown to attach to host DNA. We report the isolation of key structures, seen after induction of Mu DNA replication, after cloning lac operator into Mu DNA and using the lac repressor-operator interaction to trap Mu DNA on nitrocellulose filters. We have localized Mu sequences within these structures in the electron microscope by visualizing the lac operator-repressor interaction after binding with ferritin-conjugated antibody. This analysis shows that key structures contain replicating Mu DNA linked to non-Mu DNA and that replication can begin at either end of Mu.

MeSH Terms
Bacteriophage mu/physiology Base Sequence DNA Replication DNA Restriction Enzymes DNA Transposable Elements DNA, Recombinant DNA, Viral/physiology Lac Operon Recombination, Genetic Repressor Proteins/metabolism Virus Replication
Chemicals
DNA Transposable Elements DNA, Recombinant DNA, Viral Repressor Proteins DNA Restriction Enzymes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Harshey R M
McKay R
Bukhari A I
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1982-06-00
Pages
561-71
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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