Evidence from comparative genomics for a complete sexual cycle in the asexual pathogenic yeast Candida glabrata.docVIP
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Evidence from comparative genomics for a complete sexual cycle in the asexual pathogenic yeast Candida glabrata
Open Access
Research
Evidence from comparative genomics for a complete sexual cycle
in the ‘asexual’ pathogenic yeast Candida glabrata
Simon Wong*, Mario A Fares*, Wolfgang Zimmermann?, Geraldine Butler?
and Kenneth H Wolfe*
Addresses: *Department of Genetics, Smurfit Institute, University of Dublin, Trinity College, Dublin 2, Ireland. ?AGOWA, Glienicker Weg
185, D-12489 Berlin, Germany. ?Department of Biochemistry and Conway Institute of Biomolecular and Biomedical Research, University
College Dublin, Belfield, Dublin 4, Ireland.
Correspondence: Kenneth H Wolfe. E-mail: khwolfe@tcd.ie
Published: 23 January 2003
Received: 4 October 2002
Revised: 19 November 2002
Accepted: 4 December 2002
Genome Biology 2003, 4:R10
The electronic version of this article is the complete one and can be
found online at /2003/4/2/R10
? 2003 Wong et al.; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all
media for any purpose, provided this notice is preserved along with the articles original URL.
Abstract
Background: Candida glabrata is a pathogenic yeast of increasing medical concern. It has been
regarded as asexual since it was first described in 1917, yet phylogenetic analyses have revealed
that it is more closely related to sexual yeasts than other Candida species. We show here that the
C. glabrata genome contains many genes apparently involved in sexual reproduction.
Results: By genome survey sequencing, we find that genes involved in mating and meiosis are as
numerous in C. glabrata as in the sexual species Kluyveromyces delphensis, which is its closest
known relative. C. glabrata has a putative mating-type (MAT) locus and a pheromone gene
(MFALPHA2), as well as orthologs of at least 31 other Saccharomyces cerevisiae genes that have no
known roles apart from mating or meiosis, including FUS3, IME1 and SMK1.
Conclusions: We infer that C.
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