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<pubDate>Thu, 21 Aug 2008 14:19:55 BST</pubDate>


	<title>CiteULike: stajich's candida</title>
	<description>CiteULike: stajich's candida</description>


	<link>http://www.citeulike.org/user/stajich/tag/candida</link>
	<dc:publisher>CiteULike.org</dc:publisher>
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        <rdf:li rdf:resource="http://www.citeulike.org/user/stajich/article/3023371"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/stajich/article/2785922"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/stajich/article/2762170"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/stajich/article/1768468"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/stajich/article/984774"/>

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<item rdf:about="http://www.citeulike.org/user/stajich/article/3023371">
    <title>The asexual yeast Candida glabrata maintains distinct a and alpha haploid mating types.</title>
    <link>http://www.citeulike.org/user/stajich/article/3023371</link>
    <description>&lt;i&gt;Eukaryotic cell, Vol. 7, No. 5. (May 2008), pp. 848-858.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The genome of the type strain of Candida glabrata (CBS138, ATCC 2001) contains homologs of most of the genes involved in mating in Saccharomyces cerevisiae, starting with the mating pheromone and receptor genes. Only haploid cells are ever isolated, but C. glabrata strains of both mating types are commonly found, the type strain being MAT alpha and most other strains, such as BG2, being MATa. No sexual cycle has been documented for this species. In order to understand which steps of the mating pathway are defective, we have analyzed the expression of homologs of some of the key genes involved as well as the production of mating pheromones and the organism's sensitivity to artificial pheromones. We show that cells of opposite mating types express both pheromone receptor genes and are insensitive to pheromones. Nonetheless, cells maintain specificity through regulation of the alpha1 and alpha2 genes and, more surprisingly, through differential splicing of the a1 transcript.</description>
    <dc:title>The asexual yeast Candida glabrata maintains distinct a and alpha haploid mating types.</dc:title>

    <dc:creator>H Muller</dc:creator>
    <dc:creator>C Hennequin</dc:creator>
    <dc:creator>J Gallaud</dc:creator>
    <dc:creator>B Dujon</dc:creator>
    <dc:creator>C Fairhead</dc:creator>
    <dc:identifier>doi:10.1128/EC.00456-07</dc:identifier>
    <dc:source>Eukaryotic cell, Vol. 7, No. 5. (May 2008), pp. 848-858.</dc:source>
    <dc:date>2008-07-21T03:13:41-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Eukaryotic cell</prism:publicationName>
    <prism:issn>1535-9786</prism:issn>
    <prism:volume>7</prism:volume>
    <prism:number>5</prism:number>
    <prism:startingPage>848</prism:startingPage>
    <prism:endingPage>858</prism:endingPage>
    <prism:category>candida</prism:category>
    <prism:category>fungi</prism:category>
    <prism:category>genome</prism:category>
    <prism:category>mating_genes</prism:category>
    <prism:category>mating_type</prism:category>
    <prism:category>saccharomyces</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/stajich/article/2785922">
    <title>Complete mitochondrial genome sequence of the wine yeast Candida zemplinina: intraspecies distribution of a novel group-IIB1 intron with eubacterial affiliations.</title>
    <link>http://www.citeulike.org/user/stajich/article/2785922</link>
    <description>&lt;i&gt;FEMS yeast research, Vol. 8, No. 2. (March 2008), pp. 311-327.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The mtDNA of the ascomycetous wine yeast Candida zemplinina is a circularly mapping genome of 23,114 bp. It contains 35 genes coding for the seven basic subunits of oxidative phosporylation found in yeasts (the genes encoding for NADH oxidoreductase subunits are absent), the ribosomal protein Var1, two rRNAs and 25 tRNA genes. Although protein phylogenetic analysis showed a divergent mitochondrial genome, several traits appeared preserved. The conserved gene blocks between the mtDNAs of C. zemplinina and Candida glabrata were maintained and changes in gene order and putative promoters were due to restricted genome reshuffling. New heterogeneous hairpin elements were identified scattered throughout cox1 introns. The large subunit rRNA gene harboured the first group-IIB1 intron containing a putative active reverse transcriptase (RT) in mitochondrial genomes of fungi. Phylogenetic analysis of the RT protein confirmed its closer relationship to eubacterial intronic RTs, while being only distantly related to all other fungal mitochondrial group-II introns and RTs. The findings point towards an early migration event of a eubacterial group-II intron to the mitochondrial genome of C. zemplinina.</description>
    <dc:title>Complete mitochondrial genome sequence of the wine yeast Candida zemplinina: intraspecies distribution of a novel group-IIB1 intron with eubacterial affiliations.</dc:title>

    <dc:creator>PV Pramateftaki</dc:creator>
    <dc:creator>VN Kouvelis</dc:creator>
    <dc:creator>P Lanaridis</dc:creator>
    <dc:creator>MA Typas</dc:creator>
    <dc:identifier>doi:10.1111/j.1567-1364.2007.00332.x</dc:identifier>
    <dc:source>FEMS yeast research, Vol. 8, No. 2. (March 2008), pp. 311-327.</dc:source>
    <dc:date>2008-05-11T22:44:19-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>FEMS yeast research</prism:publicationName>
    <prism:issn>1567-1356</prism:issn>
    <prism:volume>8</prism:volume>
    <prism:number>2</prism:number>
    <prism:startingPage>311</prism:startingPage>
    <prism:endingPage>327</prism:endingPage>
    <prism:category>candida</prism:category>
    <prism:category>evolution</prism:category>
    <prism:category>intron</prism:category>
    <prism:category>yeast</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/stajich/article/2762170">
    <title>The Parasexual Cycle in Candida albicans Provides an Alternative Pathway to Meiosis for the Formation of Recombinant Strains</title>
    <link>http://www.citeulike.org/user/stajich/article/2762170</link>
    <description>&lt;i&gt;PLoS Biology, Vol. 6, No. 5. (1 May 2008), e110.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Candida albicans has an elaborate, yet efficient, mating system that promotes conjugation between diploid a and &#945; strains. The product of mating is a tetraploid a/&#945; cell that must undergo a reductional division to return to the diploid state. Despite the presence of several &#8220;meiosis-specific&#8221; genes in the C. albicans genome, a meiotic program has not been observed. Instead, tetraploid products of mating can be induced to undergo efficient, random chromosome loss, often producing strains that are diploid, or close to diploid, in ploidy. Using SNP and comparative genome hybridization arrays we have now analyzed the genotypes of products from the C. albicans parasexual cycle. We show that the parasexual cycle generates progeny strains with shuffled combinations of the eight C. albicans chromosomes. In addition, several isolates had undergone extensive genetic recombination between homologous chromosomes, including multiple gene conversion events. Progeny strains exhibited altered colony morphologies on laboratory media, demonstrating that the parasexual cycle generates phenotypic variants of C. albicans. In several fungi, including Saccharomyces cerevisiae and Schizosaccharomyces pombe, the conserved Spo11 protein is integral to meiotic recombination, where it is required for the formation of DNA double-strand breaks. We show that deletion of SPO11 prevented genetic recombination between homologous chromosomes during the C. albicans parasexual cycle. These findings suggest that at least one meiosis-specific gene has been re-programmed to mediate genetic recombination during the alternative parasexual life cycle of C. albicans. We discuss, in light of the long association of C. albicans with warm-blooded animals, the potential advantages of a parasexual cycle over a conventional sexual cycle.</description>
    <dc:title>The Parasexual Cycle in Candida albicans Provides an Alternative Pathway to Meiosis for the Formation of Recombinant Strains</dc:title>

    <dc:creator>Anja Forche</dc:creator>
    <dc:creator>Kevin Alby</dc:creator>
    <dc:creator>Dana Schaefer</dc:creator>
    <dc:creator>Alexander Johnson</dc:creator>
    <dc:creator>Judith Berman</dc:creator>
    <dc:creator>Richard Bennett</dc:creator>
    <dc:identifier>doi:10.1371/journal.pbio.0060110</dc:identifier>
    <dc:source>PLoS Biology, Vol. 6, No. 5. (1 May 2008), e110.</dc:source>
    <dc:date>2008-05-06T17:56:05-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>PLoS Biology</prism:publicationName>
    <prism:volume>6</prism:volume>
    <prism:number>5</prism:number>
    <prism:startingPage>e110</prism:startingPage>
    <prism:category>candida</prism:category>
    <prism:category>meiosis</prism:category>
    <prism:category>parasexual</prism:category>
    <prism:category>recombination</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/stajich/article/1768468">
    <title>Computational and experimental approaches double the number of known introns in the pathogenic yeast Candida albicans</title>
    <link>http://www.citeulike.org/user/stajich/article/1768468</link>
    <description>&lt;i&gt;Genome Res., Vol. 17, No. 4. (1 April 2007), pp. 492-502.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Candida albicans is the most common fungal pathogen of humans. Frequently found as a commensal within the digestive tracts of healthy individuals, C. albicans is an opportunistic pathogen that causes a wide variety of clinical syndromes in immuno-compromised individuals. A comprehensive annotation of the C. albicans genome sequence was recently published. Because many C. albicans coding sequences are interrupted by introns, proper intron annotation is essential for the accurate definition of genes in this pathogen. Intron annotation is also important for identifying potential targets of splicing regulation, a common mechanism of gene control in eukaryotes. In this study, we report an improved annotation of C. albicans introns. In addition to correcting the existing intron annotations, 25% of which were incorrect, we have used novel computational and experimental approaches to identify new introns, bringing the total to 415, almost double the number previously known. Our identification methods focus primarily on intron features rather than protein-coding features, overcoming biases of traditional intron annotation methods. Introns are not randomly distributed in C. albicans, and are over-represented in genes involved in specific cellular processes, such as splicing, translation, and mitochondrial respiration. This nonrandom distribution suggests functional roles for these introns, and we demonstrate that splicing of two transcripts whose introns have unusual sequence features is responsive to environmental factors. 10.1101/gr.6111907</description>
    <dc:title>Computational and experimental approaches double the number of known introns in the pathogenic yeast Candida albicans</dc:title>

    <dc:creator>Quinn Mitrovich</dc:creator>
    <dc:creator>Brian Tuch</dc:creator>
    <dc:creator>Christine Guthrie</dc:creator>
    <dc:creator>Alexander Johnson</dc:creator>
    <dc:identifier>doi:10.1101/gr.6111907</dc:identifier>
    <dc:source>Genome Res., Vol. 17, No. 4. (1 April 2007), pp. 492-502.</dc:source>
    <dc:date>2007-10-15T01:00:58-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>Genome Res.</prism:publicationName>
    <prism:volume>17</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>492</prism:startingPage>
    <prism:endingPage>502</prism:endingPage>
    <prism:category>candida</prism:category>
    <prism:category>intron</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/stajich/article/984774">
    <title>Purification and characterization of an autoregulatory substance capable of regulating the morphological transition in Candida albicans</title>
    <link>http://www.citeulike.org/user/stajich/article/984774</link>
    <description>&lt;i&gt;PNAS, Vol. 98, No. 8. (10 April 2001), pp. 4664-4668.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;10.1073/pnas.071404698</description>
    <dc:title>Purification and characterization of an autoregulatory substance capable of regulating the morphological transition in Candida albicans</dc:title>

    <dc:creator>Ki-Bong Oh</dc:creator>
    <dc:creator>Hiroshi Miyazawa</dc:creator>
    <dc:creator>Toshimichi Naito</dc:creator>
    <dc:creator>Hideaki Matsuoka</dc:creator>
    <dc:source>PNAS, Vol. 98, No. 8. (10 April 2001), pp. 4664-4668.</dc:source>
    <dc:date>2006-12-08T20:34:14-00:00</dc:date>
    <prism:publicationYear>2001</prism:publicationYear>
    <prism:publicationName>PNAS</prism:publicationName>
    <prism:volume>98</prism:volume>
    <prism:number>8</prism:number>
    <prism:startingPage>4664</prism:startingPage>
    <prism:endingPage>4668</prism:endingPage>
    <prism:category>candida</prism:category>
    <prism:category>development</prism:category>
    <prism:category>fungi</prism:category>
    <prism:category>hyphael</prism:category>
    <prism:category>yeast</prism:category>
</item>



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