Cécile Fairhead

Prof. Cécile Fairhead

Université Paris-Saclay, France

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2004 in Nature
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Journal Article
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BDBernard Dujon
Bernard Dujon
DSDavid Sherman
David Sherman
GFGilles Fischer
Gilles Fischer
PDPascal Durrens
Pascal Durrens
SCSerge Casaregola
Serge Casaregola
JSJean-Luc Souciet
Jean-Luc Souciet

1 May 1992 in Nature
Verified
Journal Article
Closed access
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SOS. G. Oliver
S. G. Oliver
QAQ. J. M. van der Aart
Q. J. M. van der Aart
MAM. L. Agostoni-Carbone
M. L. Agostoni-Carbone
MAM. Aigle
M. Aigle
LALilia Alberghina
Lilia Alberghina
JSJ. G. Sgouros
J. G. Sgouros

16 August 2010 in Biological Reviews
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SBSylvain Billiard
Sylvain Billiard
MLManuela López-Villavicencio
Manuela López-Villavicencio
BDBenjamin Devier
Benjamin Devier
MHMichael E. Hood
Michael E. Hood
CFCécile Fairhead
Cécile Fairhead
TGTatiana Giraud
Tatiana Giraud

1 January 2013 in BMC Genomics
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Journal Article
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TGToni Gabaldon
Toni Gabaldon
TMTiphaine Martin
Tiphaine Martin
MMMarina Marcet-Hoiben
Marina Marcet-Hoiben
PDPascal Durrens
Pascal Durrens
MBMonique Bolotin-Fukuhara
Monique Bolotin-Fukuhara
CFCécile Fairhead
Cécile Fairhead
Candida glabrata follows C. albicans as the second or third most prevalent cause of candidemia worldwide. These two pathogenic yeasts are distantly related, C. glabrata being part of the Nakaseomyces, a group more closely related to Saccharomyces cerevisiae. Although C. glabrata was thought to be the only pathogenic Nakaseomyces, two new pathogens have recently been described within this group: C. nivariensis and C. bracarensis. To gain insight into the genomic changes underlying the emergence of virulence, we sequenced the genomes of these two, and three other non-pathogenic Nakaseomyces, and compared them to other sequenced yeasts.

4 November 1999 in Nature
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MRMiria Ricchetti
Miria Ricchetti
CFCécile Fairhead
Cécile Fairhead
BDBernard Dujon
Bernard Dujon

12 June 2009 in Genome Research
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Journal Article
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TCThe Génolevures Consortium
The Génolevures Consortium
JSJean-Luc Souciet
Jean-Luc Souciet
BDBernard Dujon
Bernard Dujon
CGClaude Gaillardin
Claude Gaillardin
MJMark Johnston
Mark Johnston
ETEmmanuel Talla
Emmanuel Talla
Our knowledge of yeast genomes remains largely dominated by the extensive studies on Saccharomyces cerevisiae and the consequences of its ancestral duplication, leaving the evolution of the entire class of hemiascomycetes only partly explored. We concentrate here on five species of Saccharomycetaceae, a large subdivision of hemiascomycetes, that we call “protoploid” because they diverged from the S. cerevisiae lineage prior to its genome duplication. We determined the complete genome sequences of three of these species: Kluyveromyces (Lachancea) thermotolerans and Saccharomyces (Lachancea) kluyveri (two members of the newly described Lachancea clade), and Zygosaccharomyces rouxii. We included in our comparisons the previously available sequences of Kluyveromyces lactis and Ashbya (Eremothecium) gossypii. Despite their broad evolutionary range and significant individual variations in each lineage, the five protoploid Saccharomycetaceae share a core repertoire of approximately 3300 protein families and a high degree of conserved synteny. Synteny blocks were used to define gene orthology and to infer ancestors. Far from representing minimal genomes without redundancy, the five protoploid yeasts contain numerous copies of paralogous genes, either dispersed or in tandem arrays, that, altogether, constitute a third of each genome. Ancient, conserved paralogs as well as novel, lineage-specific paralogs were identified.