Author
Listed:
- John F. Heidelberg
(The Institute for Genomic Research)
- Jonathan A. Eisen
(The Institute for Genomic Research)
- William C. Nelson
(The Institute for Genomic Research)
- Rebecca A. Clayton
- Michelle L. Gwinn
(The Institute for Genomic Research)
- Robert J. Dodson
(The Institute for Genomic Research)
- Daniel H. Haft
(The Institute for Genomic Research)
- Erin K. Hickey
(The Institute for Genomic Research)
- Jeremy D. Peterson
(The Institute for Genomic Research)
- Lowell Umayam
(The Institute for Genomic Research)
- Steven R. Gill
(The Institute for Genomic Research)
- Karen E. Nelson
(The Institute for Genomic Research)
- Timothy D. Read
(The Institute for Genomic Research)
- Hervé Tettelin
(The Institute for Genomic Research)
- Delwood Richardson
(The Institute for Genomic Research)
- Maria D. Ermolaeva
(The Institute for Genomic Research)
- Jessica Vamathevan
(The Institute for Genomic Research)
- Steven Bass
(The Institute for Genomic Research)
- Haiying Qin
(The Institute for Genomic Research)
- Ioana Dragoi
(The Institute for Genomic Research)
- Patrick Sellers
(The Institute for Genomic Research)
- Lisa McDonald
(The Institute for Genomic Research)
- Teresa Utterback
(The Institute for Genomic Research)
- Robert D. Fleishmann
(The Institute for Genomic Research)
- William C. Nierman
(The Institute for Genomic Research)
- Owen White
(The Institute for Genomic Research)
- Steven L. Salzberg
(The Institute for Genomic Research)
- Hamilton O. Smith
(The Institute for Genomic Research
Celera Genomics)
- Rita R. Colwell
(Center of Marine Biotechnology, University of Maryland Biotechnology Institute
University of Maryland)
- John J. Mekalanos
(Harvard Medical School)
- J. Craig Venter
(The Institute for Genomic Research
Celera Genomics)
- Claire M. Fraser
(The Institute for Genomic Research)
Abstract
Here we determine the complete genomic sequence of the Gram negative, γ-Proteobacterium Vibrio cholerae El Tor N16961 to be 4,033,460 base pairs (bp). The genome consists of two circular chromosomes of 2,961,146 bp and 1,072,314 bp that together encode 3,885 open reading frames. The vast majority of recognizable genes for essential cell functions (such as DNA replication, transcription, translation and cell-wall biosynthesis) and pathogenicity (for example, toxins, surface antigens and adhesins) are located on the large chromosome. In contrast, the small chromosome contains a larger fraction (59%) of hypothetical genes compared with the large chromosome (42%), and also contains many more genes that appear to have origins other than the γ-Proteobacteria. The small chromosome also carries a gene capture system (the integron island) and host ‘addiction’ genes that are typically found on plasmids; thus, the small chromosome may have originally been a megaplasmid that was captured by an ancestral Vibrio species. The V. cholerae genomic sequence provides a starting point for understanding how a free-living, environmental organism emerged to become a significant human bacterial pathogen.
Suggested Citation
John F. Heidelberg & Jonathan A. Eisen & William C. Nelson & Rebecca A. Clayton & Michelle L. Gwinn & Robert J. Dodson & Daniel H. Haft & Erin K. Hickey & Jeremy D. Peterson & Lowell Umayam & Steven R, 2000.
"DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae,"
Nature, Nature, vol. 406(6795), pages 477-483, August.
Handle:
RePEc:nat:nature:v:406:y:2000:i:6795:d:10.1038_35020000
DOI: 10.1038/35020000
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