A Human-Curated Annotation of the Candida albicansGenome

Burkhard R Braun(University of California, San Francisco), Marco van het Hoog(National Research Council Canada), Christophe d’Enfert(Institut Pasteur), Mikhail Martchenko(Biotechnology Research Institute), Jan Dungan(University of California, San Francisco), Alan Kuo(University of California, San Francisco), Diane O. Inglis(University of California, San Francisco), Michaël Uhl(University of California, San Francisco), Hervé Hogues(National Academies of Sciences, Engineering, and Medicine), Matthew Berriman(Wellcome Sanger Institute), Michael Lorenz(The University of Texas Health Science Center at Houston), Anastasia Levitin(Biotechnology Research Institute), Ursula Oberholzer(National Research Council Canada), Catherine Bachewich(Biotechnology Research Institute), Doreen Harcus(Biotechnology Research Institute), Anne Marcil(National Research Council Canada), Daniel Dignard(Biotechnology Research Institute), Tatiana Iouk(National Academies of Sciences, Engineering, and Medicine), Rosa Eliza Zito(National Research Council Canada), Lionel Frangeul(Institut Pasteur), Fredj Tekaia(Institut Pasteur), Kim Rutherford(Wellcome Sanger Institute), Edwin Wang(National Research Council Canada), Carol A. Munro(University of Aberdeen), Steven Bates(University of Aberdeen), Neil A. R. Gow(University of Aberdeen), Lois L. Hoyer(University of Illinois Urbana-Champaign), Gerwald A. Köhler(University of California, San Francisco), Joachim Morschhäuser(University of Würzburg), George Newport(University of California, San Francisco), Sadri Znaidi(Montreal Clinical Research Institute), Martine Raymond(Université de Montréal), Bernard Turcotte(McGill University), Gavin Sherlock(Stanford University), Maria C. Costanzo(Stanford University), Jan Ihmels(Weizmann Institute of Science), Judith Berman(University of Minnesota), Dominique Sanglard(University of Lausanne), Nina Agabian(University of California, San Francisco), Aaron P. Mitchell(Columbia University), Alexander D. Johnson(University of California, San Francisco), Malcolm Whiteway(Biotechnology Research Institute), André Nantel(National Academies of Sciences, Engineering, and Medicine)
PLoS Genetics
June 17, 2005
Cited by 338Open Access
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Abstract

Recent sequencing and assembly of the genome for the fungal pathogen Candida albicans used simple automated procedures for the identification of putative genes. We have reviewed the entire assembly, both by hand and with additional bioinformatic resources, to accurately map and describe 6,354 genes and to identify 246 genes whose original database entries contained sequencing errors (or possibly mutations) that affect their reading frame. Comparison with other fungal genomes permitted the identification of numerous fungus-specific genes that might be targeted for antifungal therapy. We also observed that, compared to other fungi, the protein-coding sequences in the C. albicans genome are especially rich in short sequence repeats. Finally, our improved annotation permitted a detailed analysis of several multigene families, and comparative genomic studies showed that C. albicans has a far greater catabolic range, encoding respiratory Complex 1, several novel oxidoreductases and ketone body degrading enzymes, malonyl-CoA and enoyl-CoA carriers, several novel amino acid degrading enzymes, a variety of secreted catabolic lipases and proteases, and numerous transporters to assimilate the resulting nutrients. The results of these efforts will ensure that the Candida research community has uniform and comprehensive genomic information for medical research as well as for future diagnostic and therapeutic applications.


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