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The nucleotide sequence of Saccharomyces cerevisiae chromosome VII

Author

Listed:
  • H. Tettelin

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • M. L. Agostoni Carbone

    (Università di Milano)

  • K. Albermann

    (Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie)

  • M. Albers

    (Institut für Biologie IV, Mikrobiologie)

  • J. Arroyo

    (Universidad Complutense)

  • U. Backes

    (Institut für Biologie IV, Mikrobiologie)

  • T. Barreiros

    (Laboratorio de Genetica Molecular, Instituto Gulbenkian de Ciencia)

  • I. Bertani

    (International Center for Genetic Engineering and Biotechnology)

  • A. J. Bjourson

    (The Queens University of Belfast)

  • M. Brückner

    (Genotype GmbH)

  • C. V. Bruschi

    (International Center for Genetic Engineering and Biotechnology)

  • G. Carignani

    (Università di Padova)

  • L. Castagnoli

    (Università di Roma ‘Tor Vergata’)

  • E. Cerdan

    (Universidad de La Coruna)

  • M. L. Clemente

    (Università di Padova)

  • A. Coblenz

    (Institut für Biologie IV, Mikrobiologie)

  • M. Coglievina

    (International Center for Genetic Engineering and Biotechnology)

  • E. Coissac

    (Centre de Génétique Moléculaire, CNRS, Laboratoire Associé à l’Université Pierre et Marie Curie)

  • E. Defoor

    (Katholieke Universiteit Leuven, Laboratory of Gene Technology)

  • S. Del Bino

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • H. Delius

    (Deutsches Krebsforschungszentrum)

  • D. Delneri

    (International Center for Genetic Engineering and Biotechnology)

  • P. de Wergifosse

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • B. Dujon

    (Institut Pasteur)

  • P. Durand

    (Faculté Universitaire des Sciences Agronomiques de Gembloux)

  • K. D. Entian

    (Institut für Mikrobiologie der Johann Wolfgang Goethe-Universität Frankfurt/Main)

  • P. Eraso

    (Instituto de Investigaciones Biomédicas del C.S.I.C.y)

  • V. Escribano

    (Instituto de Investigaciones Biomédicas del C.S.I.C.y)

  • L. Fabiani

    (Università di Roma La Sapienza)

  • B. Fartmann

    (Institut für Molekulare Genetik, Georg-August-Universität
    MWG-BIOTECH GmbH)

  • F. Feroli

    (Università di Padova)

  • M. Feuermann

    (Université Louis Pasteur/CNRS, Institut de Botanique)

  • L. Frontali

    (Università di Roma La Sapienza)

  • M. García-Gonzalez

    (Universidad Complutense
    Centro de Biotecnología)

  • M. I. García-Sáez

    (Universidad Complutense)

  • A. Goffeau

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • P. Guerreiro

    (Laboratorio de Genetica Molecular, Instituto Gulbenkian de Ciencia)

  • J. Hani

    (Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie)

  • M. Hansen

    (Institut für Biologie IV, Mikrobiologie)

  • U. Hebling

    (Deutsches Krebsforschungszentrum)

  • K. Hernandez

    (Microsynth GmbH)

  • K. Heumann

    (Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie)

  • F. Hilger

    (Faculté Universitaire des Sciences Agronomiques de Gembloux)

  • B. Hofmann

    (Deutsches Krebsforschungszentrum)

  • K. J. Indge

    (UMIST)

  • C. M. James

    (UMIST)

  • R. Klima

    (International Center for Genetic Engineering and Biotechnology)

  • P. Kötter

    (Institut für Mikrobiologie der Johann Wolfgang Goethe-Universität Frankfurt/Main)

  • B. Kramer

    (Institut für Molekulare Genetik, Georg-August-Universität
    Abteilung Klinische Biochemie, Zentrum Innere Medizin, Georg-August-Universität)

  • W. Kramer

    (Institut für Molekulare Genetik, Georg-August-Universität)

  • G. Lauquin

    (Institut de Biochimie Cellulaire, CNRS)

  • H. Leuther

    (Institut für Biologie IV, Mikrobiologie)

  • E. J. Louis

    (Yeast Genetics, Institute of Molecular Medicine, John Radcliffe Hospital)

  • E. Maillier

    (Centre de Génétique Moléculaire, CNRS, Laboratoire Associé à l’Université Pierre et Marie Curie)

  • A. Marconi

    (Università di Roma La Sapienza)

  • E. Martegani

    (Università di Milano)

  • M. J. Mazón

    (Instituto de Investigaciones Biomédicas del C.S.I.C.y)

  • C. Mazzoni

    (Università di Roma La Sapienza)

  • A. D. K. McReynolds

    (The Queens University of Belfast)

  • P. Melchioretto

    (Università di Milano)

  • H. W. Mewes

    (Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie)

  • O. Minenkova

    (Università di Roma ‘Tor Vergata’)

  • S. Müller-Auer

    (Genotype GmbH)

  • A. Nawrocki

    (Institute of Microbiology, Wroclaw University)

  • P. Netter

    (Centre de Génétique Moléculaire, CNRS, Laboratoire Associé à l’Université Pierre et Marie Curie)

  • R. Neu

    (Institut für Biologie IV, Mikrobiologie)

  • C. Nombela

    (Universidad Complutense)

  • S. G. Oliver

    (UMIST)

  • L. Panzeri

    (Università di Milano)

  • S. Paoluzi

    (Università di Roma ‘Tor Vergata’)

  • P. Plevani

    (Università di Milano)

  • D. Portetelle

    (Faculté Universitaire des Sciences Agronomiques de Gembloux)

  • F. Portillo

    (Instituto de Investigaciones Biomédicas del C.S.I.C.y)

  • S. Potier

    (Université Louis Pasteur/CNRS, Institut de Botanique)

  • B. Purnelle

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • M. Rieger

    (Genotype GmbH)

  • L. Riles

    (Washington University School of Medicine)

  • T. Rinaldi

    (Università di Roma La Sapienza)

  • J. Robben

    (Katholieke Universiteit Leuven, Laboratory of Gene Technology)

  • C. Rodrigues-Pousada

    (Laboratorio de Genetica Molecular, Instituto Gulbenkian de Ciencia)

  • E. Rodriguez-Belmonte

    (Universidad de La Coruna)

  • A. M. Rodriguez-Torres

    (Universidad de La Coruna)

  • M. Rose

    (Institut für Mikrobiologie der Johann Wolfgang Goethe-Universität Frankfurt/Main)

  • M. Ruzzi

    (Università della Tuscia)

  • M. Saliola

    (Università di Roma La Sapienza)

  • M. Sánchez-Perez

    (Universidad Complutense)

  • B. Schäfer

    (Institut für Biologie IV, Mikrobiologie)

  • M. Schäfer

    (Genotype GmbH)

  • M. Scharfe

    (AGON GmbH)

  • T. Schmidheini

    (Microsynth GmbH)

  • A. Schreer

    (Institut für Biologie IV, Mikrobiologie)

  • J. Skala

    (Institute of Microbiology, Wroclaw University)

  • J. L. Souciet

    (Université Louis Pasteur/CNRS, Institut de Botanique)

  • H. Y. Steensma

    (Institute for Molecular Plant Sciences, Leiden University
    Delft University of Technology)

  • E. Talla

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • A. Thierry

    (Institut Pasteur)

  • M. Vandenbol

    (Faculté Universitaire des Sciences Agronomiques de Gembloux)

  • Q. J. M. van der Aart

    (Institute for Molecular Plant Sciences, Leiden University)

  • L. Van Dyck

    (Unité de Biochimie Physiologique, Université Catholique de Louvain)

  • M. Vanoni

    (Università di Milano)

  • P. Verhasselt

    (Katholieke Universiteit Leuven, Laboratory of Gene Technology)

  • M. Voet

    (Katholieke Universiteit Leuven, Laboratory of Gene Technology)

  • G. Volckaert

    (Katholieke Universiteit Leuven, Laboratory of Gene Technology)

  • R. Wambutt

    (AGON GmbH)

  • M. D. Watson

    (University of Durham)

  • N. Weber

    (Microsynth GmbH)

  • E. Wedler

    (AGON GmbH)

  • H. Wedler

    (AGON GmbH)

  • P. Wipfli

    (Microsynth GmbH)

  • K. Wolf

    (Institut für Biologie IV, Mikrobiologie)

  • L. F. Wright

    (The Queens University of Belfast)

  • P. Zaccaria

    (International Center for Genetic Engineering and Biotechnology)

  • M. Zimmermann

    (Institut für Biologie IV, Mikrobiologie)

  • A. Zollner

    (Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie)

  • K. Kleine

    (Martinsrieder Institut für Protein Sequenzen, Max-Planck-Institut für Biochemie)

Abstract

The complete nucleotide sequence of Saccharomyces cerevisiae chromosome VII has 572 predicted open reading frames (ORFs), of which 341 are new. No correlation was found between G+C content and gene density along the chromosome, and their variations are random. Of the ORFs, 17% show high similarity to human proteins. Almost half of the ORFs could be classified in functional categories, and there is a slight increase in the number of transcription (7.0 %) and translation (5.2 %) factors when compared with the complete S. cerevisiae genome. Accurate verification procedures demonstrate that there are less than two errors per 10,000 base pairs in the published sequence.

Suggested Citation

  • H. Tettelin & M. L. Agostoni Carbone & K. Albermann & M. Albers & J. Arroyo & U. Backes & T. Barreiros & I. Bertani & A. J. Bjourson & M. Brückner & C. V. Bruschi & G. Carignani & L. Castagnoli & E. C, 1997. "The nucleotide sequence of Saccharomyces cerevisiae chromosome VII," Nature, Nature, vol. 387(6632), pages 81-84, May.
  • Handle: RePEc:nat:nature:v:387:y:1997:i:6632:d:10.1038_387s081
    DOI: 10.1038/387s081
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