The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics

Lincoln Stein(Cold Spring Harbor Laboratory), Zhirong Bao(University of Washington), Darin Blasiar(Washington University in St. Louis), Thomas Blumenthal(University of Colorado Denver), Michael R. Brent(Washington University in St. Louis), Nansheng Chen(Cold Spring Harbor Laboratory), Asif Chinwalla(Washington University in St. Louis), Laura Clarke(Wellcome Sanger Institute), Chris M. Clee(Wellcome Sanger Institute), Avril Coghlan(Trinity College Dublin), Alan Coulson(MRC Laboratory of Molecular Biology), Peter D’Eustachio(Cold Spring Harbor Laboratory), David Fitch(New York University), Lucinda A. Fulton(Washington University in St. Louis), Robert E. Fulton(Washington University in St. Louis), Sam Griffiths‐Jones(Washington University in St. Louis), Todd Harris(Cold Spring Harbor Laboratory), LaDeana Hillier(University of Washington), Ravi S. Kamath(Wellcome Sanger Institute), Patricia E. Kuwabara(Wellcome Sanger Institute), Elaine R. Mardis(Washington University in St. Louis), Marco A. Marra(BC Cancer Agency), Tracie L. Miner(Washington University in St. Louis), Patrick Minx(Washington University in St. Louis), James C. Mullikin(National Institutes of Health), R. W. Plumb(Wellcome Sanger Institute), Jane Rogers(Wellcome Sanger Institute), Jacqueline E. Schein(BC Cancer Agency), Marc Sohrmann(Wellcome Sanger Institute), John Spieth(Washington University in St. Louis), Jason Stajich(Duke University), Chaochun Wei(Washington University in St. Louis), David L. Willey(Wellcome Sanger Institute), Richard K. Wilson(Washington University in St. Louis), Richard Durbin(Wellcome Sanger Institute), R Waterston(University of Washington)
PLoS Biology
November 14, 2003
Cited by 958Open Access
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Abstract

The soil nematodes Caenorhabditis briggsae and Caenorhabditis elegans diverged from a common ancestor roughly 100 million years ago and yet are almost indistinguishable by eye. They have the same chromosome number and genome sizes, and they occupy the same ecological niche. To explore the basis for this striking conservation of structure and function, we have sequenced the C. briggsae genome to a high-quality draft stage and compared it to the finished C. elegans sequence. We predict approximately 19,500 protein-coding genes in the C. briggsae genome, roughly the same as in C. elegans. Of these, 12,200 have clear C. elegans orthologs, a further 6,500 have one or more clearly detectable C. elegans homologs, and approximately 800 C. briggsae genes have no detectable matches in C. elegans. Almost all of the noncoding RNAs (ncRNAs) known are shared between the two species. The two genomes exhibit extensive colinearity, and the rate of divergence appears to be higher in the chromosomal arms than in the centers. Operons, a distinctive feature of C. elegans, are highly conserved in C. briggsae, with the arrangement of genes being preserved in 96% of cases. The difference in size between the C. briggsae (estimated at approximately 104 Mbp) and C. elegans (100.3 Mbp) genomes is almost entirely due to repetitive sequence, which accounts for 22.4% of the C. briggsae genome in contrast to 16.5% of the C. elegans genome. Few, if any, repeat families are shared, suggesting that most were acquired after the two species diverged or are undergoing rapid evolution. Coclustering the C. elegans and C. briggsae proteins reveals 2,169 protein families of two or more members. Most of these are shared between the two species, but some appear to be expanding or contracting, and there seem to be as many as several hundred novel C. briggsae gene families. The C. briggsae draft sequence will greatly improve the annotation of the C. elegans genome. Based on similarity to C. briggsae, we found strong evidence for 1,300 new C. elegans genes. In addition, comparisons of the two genomes will help to understand the evolutionary forces that mold nematode genomes.


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