Progress, and Applications
of the Human Genome Project
Sponsored by the U.S. Department of Energy Human Genome Program
Human Genome News Archive Edition
|Available in PDF
In this issue...
DOE '99 Oakland Highlights
In the News
Web, Other Resources, Publications
Microbial Genome Explorations
Report from 1999 DOE Genome Meeting
Analysis of microbial genomes can provide clues to genome organization and evolution, contribute to a healthy citizenry, and offer potential solutions to long-standing challenges in renewable energy production, chemical and materials production, and environmental cleanup. To take advantage of these opportunities for fulfilling key missions, in 1994 DOE initiated its Microbial Genome Program (MGP), a spinoff of the Human Genome Program. At the Oakland Contractor-Grantee meeting, MGP researchers reported exciting progress.
Scientists hope that analyzing D. radiodurans' genome will give some clues to its remarkable DNA-repair mechanisms and that the microbe will be useful in cleaning up toxic mixed-waste sites around the globe. Schwartz's optical mapping of the D. radiodurans genome was critical to the discovery that it has four chromosomal elements rather than just one [see Science 285(5433), 1558-62; HGN 10(1-2), 12].
Schwartz described using a single-molecule approach to produce ordered restriction maps from individual DNA molecules. The technique, proven useful for producing high-resolution detailed maps of clones and entire genomes, is expected to facilitate large-scale sequencing projects. Optical mapping also generates an in situ picture of the entire genome's architecture, revealing the number of chromosomes and the existence of extrachromosomal elements. The team plans to use optical mapping to complete a human reference map that will include 10x to 15x coverage and link with other physical maps by aligning restriction-mapped BAC contigs.
White discussed results of an early survey of the D. radiodurans genome to determine how this organism withstands extraordinarily high levels of radiation and oxidative stress. But so far, analysis of the DNA-repair genes has turned up nothing unique that would account for the capability to knit double-stranded breaks back together.
"They're pretty much the garden variety of DNA-repair genes," White noted. A survival strategy unique to this organism is that the genome is partitioned into regions of genes that have specific functions.
Minton discussed efforts to annotate the D. radiodurans sequence, focusing on properties that render this organism resistant to radiation. This work has been taken over by Michael Daly (USUHS). Features noted to date include a novel enzyme that combines potential repair domains from three independent repair proteins. Minton reported on Daly's work to engineer this genome to enhance the potential for organopollutant degradation in radioactive mixed-waste environments; for example, Daly introduced genes to degrade toluene to less-dangerous substances and showed that the genes retain effectiveness even at high-radiation doses.
Minton also described Daly's engineering of heavy-metal resistance by transferring a mercury-resistance gene from Escherichia coli and the team's plans to transfer a uranium-reduction gene from the microbe Shewanella putrefaciens to D. radiodurans. In Shewanella, uranium acts as a final electron acceptor, being reduced from uranium+6 to uranium+4, which settles like a stone or mineral and does not enter the groundwater.
Initial work is focused on the Pyrococcus furiosus and Methanococcus jannaschii proteomes (both genomes have been sequenced completely). Both are hyperthermophilic archaea with growth temperatures near 100oC and enzymatic capabilities that have promise for bioremediation, energy conversion, and chemical-processing systems. Investigators are using 2-DGE to purify and quantitate proteins expressed in archaea that are grown under a variety of conditions designed to modulate specific metabolic pathways. Giometti discussed preliminary results, which provide a foundation for studying the M. jannaschii and P. furiosus proteomes.
Projects have begun to leverage microbial sequence information to sequence other strains more rapidly. Gary Andersen (Lawrence Livermore National Laboratory, LLNL) spoke about using suppressive subtractive hybridization to identify genomic differences among enteropathogenic strains of Yersinia enterocolitica and Y. pseudotuberculosis. The technique uses PCR amplification to enrich for unique segments of restricted DNA and simultaneously limits nontarget amplification by suppression PCR. Of the two pathogens, Y. enterocolitica is more often associated with human infection.
These explorations are likely to reveal unique DNA regions that define the genetic basis for the underlying differences in their phenotypic variation. Streamlining, automating, and increasing this technique's throughput should enable large-scale genomic comparison among closely related strains and generation of strain-specific oligonucleotide probes for molecular epidemiology studies. Ultimately, this technology could enable the much more rapid determination of closely related microbial sequences based on completed reference strain sequences.
The electronic form of the newsletter may be cited in the following
Last modified: Wednesday, October 29, 2003
Home * Contacts * Disclaimer
Document Use and Credits
Publications and webpages on this site were created by the U.S. Department of Energy Genome Program's Biological and Environmental Research Information System (BERIS). Permission to use these documents is not needed, but please credit the U.S. Department of Energy Genome Programs and provide the website http://genomics.energy.gov. All other materials were provided by third parties and not created by the U.S. Department of Energy. You must contact the person listed in the citation before using those documents.
Base URL: www.ornl.gov/hgmis
Site sponsored by the U.S. Department of Energy Office of Science, Office of Biological and Environmental Research, Human Genome Program