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PMID: 3157994 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Propagation of some human DNA sequences in bacteriophage lambda vectors requires mutant Escherichia coli hosts.

Wyman AR, Wolfe LB, Botstein D

Abstract

The growth of clones of human genomic DNA fragments in a bacteriophage lambda vector has been examined in a number of different Escherichia coli hosts. A large proportion (8.9%) of the phages carrying different fragments of the human genome fail to grow on standard rec+ hosts but will grow on hosts carrying mutations in the recB, recC, and sbcB genes. Heteroduplex analysis in the electron microscope of DNA from four of these phages revealed substantial secondary structure, including snap-back regions 200-500 base pairs in length. Such structures were not found in phages from the same DNA library that grow in rec+ hosts. These results are interpreted in the light of prior observations [Leach, D.R.F. & Stahl, F. (1983) Nature (London) 305, 448-451] showing that inverted repetitions cloned in phage lambda can be propagated in recB recC sbcB hosts but not in rec+ hosts.

MeSH Terms
Bacteriophage lambda/genetics Base Sequence Cloning, Molecular DNA, Recombinant Escherichia coli/genetics Genetic Vectors Humans Mutation Nucleic Acid Heteroduplexes/genetics Polymorphism, Genetic Repetitive Sequences, Nucleic Acid
Chemicals
DNA, Recombinant Nucleic Acid Heteroduplexes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wyman A R
Wolfe L B
Botstein D
References (13)
13 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1985-05-00
Pages
2880-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC397670
Subset
IM
Grants
NIGMS NIH HHS · GM18973 · United States
NIGMS NIH HHS · GM21253 · United States
NIGMS NIH HHS · GM30467 · United States
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