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PMID: 10373596 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

An efficient and accurate integration of mini-Mu transposons in vitro: a general methodology for functional genetic analysis and molecular biology applications.

Nucleic acids research ·Vol. 27 ·No. 13 ·1999-07-01 ·Pages 2777-84

Haapa S, Taira S, Heikkinen E, Savilahti H

Abstract

Transposons are mobile genetic elements and have been utilized as essential tools in genetics over the years. Though highly useful, many of the current transposon-based applications suffer from various limitations, the most notable of which are: (i) transposition is performed in vivo, typically species specifically, and as a multistep process; (ii) accuracy and/or efficiency of the in vivo or in vitro transposition reaction is not optimal; (iii) a limited set of target sites is used. We describe here a genetic analysis methodology that is based on bacteriophage Mu DNA transposition and circumvents such limitations. The Mu transposon tool is composed of only a few components and utilizes a highly efficient and accurate in vitro DNA transposition reaction with a low stringency of target preference. The utility of the Mu system in functional genetic analysis is demonstrated using restriction analysis and genetic footprinting strategies. The Mu methodology is readily applicable in a variety of current and emerging transposon-based techniques and is expected to generate novel approaches to functional analysis of genes, genomes and proteins.

MeSH Terms
Base Sequence DNA/analysis,genetics DNA Transposable Elements/genetics Escherichia coli Gene Expression Regulation Genetic Techniques Genome Molecular Sequence Data Proteins/analysis,genetics
Chemicals
DNA Transposable Elements Proteins DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Haapa S
Institute of Biotechnology, Viikki Biocenter, PO Box 56, Viikinkaari 9, University of Helsinki, 00014 Helsinki, Finland.
Taira S
Heikkinen E
Savilahti H
Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1999-07-01
Pages
2777-84
Language
English
Region
England
NLM ID
0411011
PMCID
PMC148488
Subset
IM
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