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[
Nature,
2003]
The genome of the microscopic worm Caenorhabditis briggsae has been sequenced, and show some remarkable differences from the genome of the better known - and physically similar - C. elegans.
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[
Science,
1990]
An exhaustive study of the tiny roundworm C. elegans has revealed a wealth of information about development and the brain. And now the effort to decipher the worm's genome is fast becoming the benchmark by which the human genome project will be measured.
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[
Science,
1998]
The near completion of the sequence of the C. elegans genome should provide researchers with a gold mine of information on topics ranging from evolution to gene
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[
Nature,
1998]
In 1983, John Sulston and Alan Coulson began to construct a complete physical map of the genome of the nematode worm Caenorhabditis elegans, and started what became known as the C. elegans Genome Project. At the time, several people wondered why John, who had just described all of the cell divisions in C. elegans (the cell lineage), was interested in this project rather than in a more 'biological' problem. He replied by joking that he had a "weakness for grandiose, meaningless projects". In 1989, as the physical map approached completion, the Genome Project, now including Bob Waterston and his group, embarked on the even more ambitious goal of obtaining the complete genomic sequence
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[
Nature,
1998]
The human genome is predicted to contain between 50,000 and 100,000 genes. To work out what these genes do, an array of techniques is needed to evaluate the protein-protein interactions and biochemical pathways of any gene product. The nematode worm Caenorhabditis elegans is an excellent system for such studies because of its well-understood genetics and development, evolutionary conservation to human genes, small genome size and relatively short life cycle. The 100-megabase-pair genome will be completely sequenced this year, and a total of 17,000 genes have been predicted, many with human counterparts. Approaches used to manipulate gene expression in C. elegans include transposon-mediated deletion, antisense inhibition and direct isolation of deletions after mutagenesis. Although these methods have proved useful, limitations still exist.
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[
Nature,
1992]
Supporters of large DNA sequencing projects will take heart (and find much to learn) from the report by J. Sulston and colleagues that appears on page 37 of this issue. Sulston et al. describe the first results of the Caenorhabditis elegans genome sequencing project, and have come up with not only hitherto unknown genes but also with fresh and biologically relevant information.
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[
Nat Genet,
1999]
One of the founders of molecular biology, Al Hershey, proffered a vision of heaven, in which one would come into the lab every morning knowing what experiment to do, knowing that it was going to work and knowing that the results would be important. Whether the authors of the Caenorhabditis elegans genome project, published recently in Science felt they had ascended into heaven while performing this gigantic piece of work is unclear, but the project seems to fulfill Hershey's criteria.
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[
Nature,
1994]
On page 32 of this issue, a joint team from the Genome Sequencing Center (St. Louis, USA) and the newly founded Sanger Centre (Hinxton Hall, Cambridge, UK) report a contiguous sequence of over two megabases from chromosome III of the nematode worm, Caenorhabditis elegans. This is the longest contiguous DNA sequence yet determined, and it prompts rumination on how far we have come in the sequencing enterprise, and on how far - and where - we have
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[
Nature,
1999]
Life is based on social contract, genes work for the good of the organism, and they are reproduced. But certain rogue genes, called transposons, wantonly reproduce at the expense of the organism, inserting new copies of themselves all over the genome. Reporting in Cell, Tabara et al., and Ketting et al. now show that organisms have systems to hold transposons in check. They suggest that one of the clues that organisms use to detect illicit activity is double-stranded RNA, and their results could explain the reason for the mysterious phenomenon of RNA interference.
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[
Nature,
1999]
Animal evolution is commonly viewed as producing diverse, environmentally adapted bodies to propagate the germ line. The evolutionary theory of ageing suggests that genetic limits to lifespan may be inadvertent consequences of evolutionary selection for maximizing that propagation. In other words, trade-offs occur that favour reproductive success over post-reproductive longevity; lifespan should be inversely correlated with fecundity when progeny production diverts resources from the maintenance of somatic (non-reproductive) cells. The germ line contains all the genetic information to specify the soma. But it is also possible that there are other, environmentally modulated instructions for life history that the germ line conveys to the soma to maximize reproduction.