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The nucleotide sequence of Saccharomyces cerevisiae chromosome XVI

H. Bussey (), R. K. Storms, Akhter Ahmed (), K. Albermann, E. Allen, W. Ansorge, R. Araujo, A. Aparicio, B. Barrell, K. Badcock, V. Benes, D. Botstein, S. Bowman, M. Brückner, J. Carpenter, J. M. Cherry, E. Chung, C. Churcher, F. Coster, K. Davis, R. W. Davis, F. S. Dietrich, H. Delius, T. DiPaolo, E. Dubois, A. Düsterhöft, M. Duncan, M. Floeth, N. Fortin, J. D. Friesen, C. Fritz, A. Goffeau, J. Hall, U. Hebling, K. Heumann, H. Hilbert, L. Hillier, S. Hunicke-Smith, R. Hyman, M. Johnston, S. Kalman, K. Kleine, C. Komp, O. Kurdi, D. Lashkari, H. Lew, A. Lin, D. Lin, E. J. Louis, R. Marathe, F. Messenguy, H. W. Mewes, S. Mirtipati, D. Moestl, S. Müller-Auer, A. Namath, U. Nentwich, P. Oefner, D. Pearson, F. X. Petel, T. M. Pohl, B. Purnelle, M. A. Rajandream, S. Rechmann, M. Rieger, L. Riles, D. Roberts, M. Schäfer, M. Scharfe, B. Scherens, S. Schramm, M. Schröder, A. M. Sdicu, H. Tettelin, L. A. Urrestarazu, S. Ushinsky, F. Vierendeels, S. Vissers, H. Voss, S. V. Walsh, R. Wambutt, Y. Wang, E. Wedler, H. Wedler, E. Winnett, W-W. Zhong, A. Zollner, D. H. Vo and J. Hani
Additional contact information
H. Bussey: McGill University
R. K. Storms: Concordia University
K. Albermann: Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie
E. Allen: Stanford University
W. Ansorge: European Molecular Biology Laboratory
R. Araujo: Stanford University
A. Aparicio: Stanford University
B. Barrell: The Sanger Centre, Wellcome Trust Genome Campus
K. Badcock: The Sanger Centre, Wellcome Trust Genome Campus
V. Benes: European Molecular Biology Laboratory
D. Botstein: Stanford University
S. Bowman: The Sanger Centre, Wellcome Trust Genome Campus
M. Brückner: Genotype GmbH
J. Carpenter: Stanford University
J. M. Cherry: Stanford University
E. Chung: Stanford University
C. Churcher: The Sanger Centre, Wellcome Trust Genome Campus
F. Coster: Unité de Biochimie Physiologique, Université Catholique de Louvain
K. Davis: Stanford University
R. W. Davis: Stanford University
F. S. Dietrich: Stanford University
H. Delius: DKFZ
T. DiPaolo: McGill University
E. Dubois: Research Institute of CERIA-COOVI
A. Düsterhöft: QIAGEN GmbH
M. Duncan: Stanford University
M. Floeth: QIAGEN GmbH
N. Fortin: McGill University
J. D. Friesen: Research Institute, Hospital for Sick Children
C. Fritz: QIAGEN GmbH
A. Goffeau: Unité de Biochimie Physiologique, Université Catholique de Louvain
J. Hall: McGill University
U. Hebling: DKFZ
K. Heumann: Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie
H. Hilbert: QIAGEN GmbH
L. Hillier: Washington University, School of Medicine
S. Hunicke-Smith: Stanford University
R. Hyman: Stanford University
M. Johnston: Washington University, School of Medicine
S. Kalman: Stanford University
K. Kleine: Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie
C. Komp: Stanford University
O. Kurdi: Stanford University
D. Lashkari: Stanford University
H. Lew: Stanford University
A. Lin: Stanford University
D. Lin: Stanford University
E. J. Louis: Yeast Genetics, Institute of Molecular Medicine, John Radcliffe Hospital
R. Marathe: Stanford University
F. Messenguy: Research Institute of CERIA-COOVI
H. W. Mewes: Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie
S. Mirtipati: Stanford University
D. Moestl: QIAGEN GmbH
S. Müller-Auer: Genotype GmbH
A. Namath: Stanford University
U. Nentwich: European Molecular Biology Laboratory
P. Oefner: Stanford University
D. Pearson: The Sanger Centre, Wellcome Trust Genome Campus
F. X. Petel: Stanford University
T. M. Pohl: Gesellschaft für Analyse Technik und Consulting mbH
B. Purnelle: Unité de Biochimie Physiologique, Université Catholique de Louvain
M. A. Rajandream: The Sanger Centre, Wellcome Trust Genome Campus
S. Rechmann: European Molecular Biology Laboratory
M. Rieger: Genotype GmbH
L. Riles: Washington University, School of Medicine
D. Roberts: Stanford University
M. Schäfer: Genotype GmbH
M. Scharfe: AGON, Gesellschaft für molekularbiologische Technologie mbH
B. Scherens: Vlaams Interuniversitair Instituut voor Biothechnologie
S. Schramm: Stanford University
M. Schröder: Stanford University
A. M. Sdicu: McGill University
H. Tettelin: Unité de Biochimie Physiologique, Université Catholique de Louvain
L. A. Urrestarazu: Laboratoire de Physiologie Cellulaire et de Génétique des Levures, Université Libre de Bruxelles
S. Ushinsky: Concordia University
F. Vierendeels: Research Institute of CERIA-COOVI
S. Vissers: Vlaams Interuniversitair Instituut voor Biothechnologie
H. Voss: European Molecular Biology Laboratory
S. V. Walsh: The Sanger Centre, Wellcome Trust Genome Campus
R. Wambutt: AGON, Gesellschaft für molekularbiologische Technologie mbH
Y. Wang: McGill University
E. Wedler: AGON, Gesellschaft für molekularbiologische Technologie mbH
H. Wedler: AGON, Gesellschaft für molekularbiologische Technologie mbH
E. Winnett: McGill University
W-W. Zhong: McGill University
A. Zollner: Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie
D. H. Vo: McGill University
J. Hani: Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie

Nature, 1997, vol. 387, issue 6632, 103-105

Abstract: Abstract The nucleotide sequence of the 948,061 base pairs of chromosome XVI has been determined, completing the sequence of the yeast genome. Chromosome XVI was the last yeast chromosome identified1, and some of the genes mapped early to it, such as GAL4, PEP4 and RAD1(ref. 2) have played important roles in the development of yeast biology. The architecture of this final chromosome seems to be typical of the large yeast chromosomes, and shows large duplications with other yeast chromosomes. Chromosome XVI contains 487 potential protein-encoding genes, 17 tRNA genes and two small nuclear RNA genes; 27% of the genes have significant similarities to human gene products, and 48% are new and of unknown biological function. Systematic efforts to explore gene function have begun.

Date: 1997
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DOI: 10.1038/387s103

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