Systematic identification of essential genes by in vitro mariner mutagenesis
Open Access
- 21 July 1998
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 95 (15) , 8927-8932
- https://doi.org/10.1073/pnas.95.15.8927
Abstract
Although the complete DNA sequences of several microbial genomes are now available, nearly 40% of the putative genes lack identifiable functions. Comprehensive screens and selections for identifying functional classes of genes are needed to convert sequence data into meaningful biological information. One particularly significant group of bacterial genes consists of those that are essential for growth or viability. Here, we describe a simple system for performing transposon mutagenesis on naturally transformable organisms along with a technique to rapidly identify essential or conditionally essential DNA segments. We show the general utility of this approach by applying it to two human pathogens, Haemophilus influenzae and Streptococcus pneumoniae, in which we detected known essential genes and assigned essentiality to several ORFs of unknown function.Keywords
This publication has 24 references indexed in Scilit:
- The Complete Genome Sequence of Escherichia coli K-12Science, 1997
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Insertional mutagenesis and rapid cloning of essential genes in zebrafishNature, 1996
- Lipoprotein e(P4) is essential for hemin uptake by Haemophilus influenzae.The Journal of Experimental Medicine, 1996
- Construction and evaluation of new drug-resistance cassettes for gene disruption mutagenesis in Streptococcus pneumoniae, using an ami test platformGene, 1995
- Whole-Genome Random Sequencing and Assembly of Haemophilus influenzae RdScience, 1995
- A double counter-selection system for the study of null alleles of essential genes in escherichia coliGene, 1995
- Carboxy-Terminal Region of Escherichia coli SecA ATPase Is Important to Promote Its Protein Translocation Activity in VivoBiochemical and Biophysical Research Communications, 1994
- Molecular analysis of Saccharomyces cerevisiae chromosome I: On the number of genes and the identification of essential genes using temperature-sensitive-lethal mutationsJournal of Molecular Biology, 1992
- In vitro transposition of bacteriophage Mu: A biochemical approach to a novel replication reactionCell, 1983