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dc.contributor.authorvan het Hoog, Marco
dc.contributor.authorRast, Timothy J
dc.contributor.authorMartchenko, Mikhail
dc.contributor.authorGrindle, Suzanne
dc.contributor.authorDignard, Daniel
dc.contributor.authorHogues, Herve
dc.contributor.authorCuomo, Christina
dc.contributor.authorBerriman, Matthew
dc.contributor.authorScherer, Stewart
dc.contributor.authorWhiteway, Malcolm
dc.contributor.authorChibana, Hiroji
dc.contributor.authorNantel, Andre
dc.contributor.authorMagee, P. T.
dc.contributor.authorMagee, B. B.
dc.date.accessioned2010-10-06T19:35:30Z
dc.date.available2010-10-06T19:35:30Z
dc.date.issued2007-04
dc.date.submitted2006-10
dc.identifier.issn1474-760X
dc.identifier.issn1465-6914
dc.identifier.urihttp://hdl.handle.net/1721.1/58917
dc.description.abstractBackground: The 10.9× genomic sequence of Candida albicans, the most important human fungal pathogen, was published in 2004. Assembly 19 consisted of 412 supercontigs, of which 266 were a haploid set, since this fungus is diploid and contains an extensive degree of heterozygosity but lacks a complete sexual cycle. However, sequences of specific chromosomes were not determined. Results: Supercontigs from Assembly 19 (183, representing 98.4% of the sequence) were assigned to individual chromosomes purified by pulse-field gel electrophoresis and hybridized to DNA microarrays. Nine Assembly 19 supercontigs were found to contain markers from two different chromosomes. Assembly 21 contains the sequence of each of the eight chromosomes and was determined using a synteny analysis with preliminary versions of the Candida dubliniensis genome assembly, bioinformatics, a sequence tagged site (STS) map of overlapping fosmid clones, and an optical map. The orientation and order of the contigs on each chromosome, repeat regions too large to be covered by a sequence run, such as the ribosomal DNA cluster and the major repeat sequence, and telomere placement were determined using the STS map. Sequence gaps were closed by PCR and sequencing of the products. The overall assembly was compared to an optical map; this identified some misassembled contigs and gave a size estimate for each chromosome. Conclusion: Assembly 21 reveals an ancient chromosome fusion, a number of small internal duplications followed by inversions, and a subtelomeric arrangement, including a new gene family, the TLO genes. Correlations of position with relatedness of gene families imply a novel method of dispersion. The sequence of the individual chromosomes of C. albicans raises interesting biological questions about gene family creation and dispersion, subtelomere organization, and chromosome evolution.en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (contract N01 AI05406)en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (grant R01 AI 16567)en_US
dc.description.sponsorshipNational Research Council (U.S.). Genome Health Initiativeen_US
dc.description.sponsorshipCanadian Institutes for Health Research (grant HOP 67260)en_US
dc.description.sponsorshipCanadian Institutes for Health Research (grant MOP 42516)en_US
dc.description.sponsorshipMinistry of Education, Culture, Sports, Science and Technology of Japan (Grant-in-Aid for Scientific Research)en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/gb-2007-8-4-r52en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleAssembly of the Candida albicans genome into sixteen supercontigs aligned on the eight chromosomesen_US
dc.typeArticleen_US
dc.identifier.citationGenome Biology. 2007 Apr 09;8(4):R52en_US
dc.contributor.departmentBroad Institute of MIT and Harvarden_US
dc.contributor.mitauthorCuomo, Christina
dc.relation.journalGenome Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2010-09-03T16:14:06Z
dc.language.rfc3066en
dc.rights.holdervan het Hoog et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsvan het Hoog, Marco; Rast, Timothy J; Martchenko, Mikhail; Grindle, Suzanne; Dignard, Daniel; Hogues, Hervé; Cuomo, Christine; Berriman, Matthew; Scherer, Stewart; Magee, BB; Whiteway, Malcolm; Chibana, Hiroji; Nantel, André; Magee, PTen
dspace.mitauthor.errortrue
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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