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PMID: 6278241 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Physical mapping of the srl recA region of Escherichia coli: analysis of Tn10 generated insertions and deletions.

Molecular & general genetics : MGG ·Vol. 183 ·No. 3 ·1981-00-00 ·Pages 497-504

Willis DK, Uhlin BE, Amini KS, Clark AJ

Abstract

A restriction endonuclease map for the enzymes EcoRI, BamHI, SalI, and PstI covering 23.5 kilobase pairs (kb) of the srl recA region of Escherichia coli was constructed. An insertion of the transposon Tn10 in the negative regulatory gene srlR was shown to be located 5.8 kb away from the promoter proximal end of the recA gene. The extent of several Tn10 generated deletions, originating from the srlR301::Tn10 insertion, were analyzed by physical mapping. Three mutations that had removed the Tn10 encoded tetracycline resistance gene, del(srl-recA)302, del(srl-recA)304, and del(srl-recA)303, were found to be deleted for 40%, 45%, and 50% of the recA structural gene, respectively. A deletion, del(srl-recA)306, that had not affected the structure of the Tn10 in srlR301 was shown to have removed the entire recA structural gene.

MeSH Terms
Chromosome Deletion Chromosome Mapping Chromosomes, Bacterial DNA Restriction Enzymes/metabolism DNA Transposable Elements DNA, Bacterial Escherichia coli/genetics Genes, Bacterial Mutation Recombination, Genetic
Chemicals
DNA Transposable Elements DNA, Bacterial DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Willis D K
Uhlin B E
Amini K S
Clark A J
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27 references, click to expand
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Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1981-00-00
Pages
497-504
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
Grants
NIAID NIH HHS · AI05371 · United States
NIGMS NIH HHS · GM07232 · United States
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