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DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288016/ https://www.ncbi.nlm.nih.gov/pubmed/10952301 http://dx.doi.org/10.1038/35020000 |
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author | Heidelberg, John F. Eisen, Jonathan A. Nelson, William C. Clayton, Rebecca A. Gwinn, Michelle L. Dodson, Robert J. Haft, Daniel H. Hickey, Erin K. Peterson, Jeremy D. Umayam, Lowell Gill, Steven R. Nelson, Karen E. Read, Timothy D. Tettelin, Hervé Richardson, Delwood Ermolaeva, Maria D. Vamathevan, Jessica Bass, Steven Qin, Haiying Dragoi, Ioana Sellers, Patrick McDonald, Lisa Utterback, Teresa Fleishmann, Robert D. Nierman, William C. White, Owen Salzberg, Steven L. Smith, Hamilton O. Colwell, Rita R. Mekalanos, John J. Venter, J. Craig Fraser, Claire M. |
author_facet | Heidelberg, John F. Eisen, Jonathan A. Nelson, William C. Clayton, Rebecca A. Gwinn, Michelle L. Dodson, Robert J. Haft, Daniel H. Hickey, Erin K. Peterson, Jeremy D. Umayam, Lowell Gill, Steven R. Nelson, Karen E. Read, Timothy D. Tettelin, Hervé Richardson, Delwood Ermolaeva, Maria D. Vamathevan, Jessica Bass, Steven Qin, Haiying Dragoi, Ioana Sellers, Patrick McDonald, Lisa Utterback, Teresa Fleishmann, Robert D. Nierman, William C. White, Owen Salzberg, Steven L. Smith, Hamilton O. Colwell, Rita R. Mekalanos, John J. Venter, J. Craig Fraser, Claire M. |
author_sort | Heidelberg, John F. |
collection | PubMed |
description | 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. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/35020000) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8288016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82880162021-07-23 DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae Heidelberg, John F. Eisen, Jonathan A. Nelson, William C. Clayton, Rebecca A. Gwinn, Michelle L. Dodson, Robert J. Haft, Daniel H. Hickey, Erin K. Peterson, Jeremy D. Umayam, Lowell Gill, Steven R. Nelson, Karen E. Read, Timothy D. Tettelin, Hervé Richardson, Delwood Ermolaeva, Maria D. Vamathevan, Jessica Bass, Steven Qin, Haiying Dragoi, Ioana Sellers, Patrick McDonald, Lisa Utterback, Teresa Fleishmann, Robert D. Nierman, William C. White, Owen Salzberg, Steven L. Smith, Hamilton O. Colwell, Rita R. Mekalanos, John J. Venter, J. Craig Fraser, Claire M. Nature Article 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. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/35020000) contains supplementary material, which is available to authorized users. Nature Publishing Group UK 2000-08-01 2000 /pmc/articles/PMC8288016/ /pubmed/10952301 http://dx.doi.org/10.1038/35020000 Text en © The Author(s) 2000 https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed under the terms of the Creative Commons Attribution-Non-Commercial-Share Alike licence (http://creativecommons.org/licenses/by-nc-sa/3.0/ (https://creativecommons.org/licenses/by-nc-sa/3.0/) ), which permits distribution, and reproduction in any medium, provided the original author and source are credited. This licence does not permit commercial exploitation, and derivative works must be licensed under the same or similar licence. |
spellingShingle | Article Heidelberg, John F. Eisen, Jonathan A. Nelson, William C. Clayton, Rebecca A. Gwinn, Michelle L. Dodson, Robert J. Haft, Daniel H. Hickey, Erin K. Peterson, Jeremy D. Umayam, Lowell Gill, Steven R. Nelson, Karen E. Read, Timothy D. Tettelin, Hervé Richardson, Delwood Ermolaeva, Maria D. Vamathevan, Jessica Bass, Steven Qin, Haiying Dragoi, Ioana Sellers, Patrick McDonald, Lisa Utterback, Teresa Fleishmann, Robert D. Nierman, William C. White, Owen Salzberg, Steven L. Smith, Hamilton O. Colwell, Rita R. Mekalanos, John J. Venter, J. Craig Fraser, Claire M. DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae |
title | DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae |
title_full | DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae |
title_fullStr | DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae |
title_full_unstemmed | DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae |
title_short | DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae |
title_sort | dna sequence of both chromosomes of the cholera pathogen vibrio cholerae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288016/ https://www.ncbi.nlm.nih.gov/pubmed/10952301 http://dx.doi.org/10.1038/35020000 |
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