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  • 1
    Publikationsdatum: 2015-05-12
    Beschreibung: Fungi from the genus Candida are common members of the human microbiota; however, they are also important opportunistic pathogens in immunocompromised hosts. Several morphological transitions have been linked to the ability of these fungi to occupy the different ecological niches in the human body. The transcription factor Efg1 from the APSES family plays a central role in the transcription circuits underlying several of these morphological changes. In Candida albicans , for example, Efg1 is a central regulator of filamentation, biofilm formation, and white-opaque switching, processes associated with survival in the human host. Orthologs of Efg1 are present throughout the Candida clade but, surprisingly, the genome sequence of Candida tropicalis failed to uncover a gene coding for Efg1. One possibility was that the paralog of Efg1, Efh1, had assumed the function of Efg1 in C. tropicalis . However, we show that this gene has only a minor role in the morphological transitions mentioned above. Instead, we report here that C. tropicalis does have an ortholog of the EFG1 gene found in other Candida species. The gene is located in a different genomic position than EFG1 in C. albicans , in a region that contains a gap in the current genome assembly of C. tropicalis . We show that the newly identified C. tropicalis EFG1 gene regulates filamentation, biofilm formation, and white-opaque switching. Our results highlight the conserved role of Efg1 in controlling morphogenesis in Candida species and remind us that published genome sequences are drafts that require continuous curation and careful scrutiny.
    Digitale ISSN: 2160-1836
    Thema: Biologie
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Publikationsdatum: 2016-03-04
    Beschreibung: The human fungal pathogen Candida albicans can switch between two cell types, "white" and "opaque," each of which is heritable through many cell divisions. Switching between these two cell types is regulated by six transcriptional regulators that form a highly interconnected circuit with multiple feedback loops. Here, we identify a seventh regulator of white-opaque switching, which we have named Wor4. We show that ectopic expression of Wor4 is sufficient to drive switching from the white to the opaque cell type, and that deletion of Wor4 blocks switching from the white to the opaque cell type. A combination of ectopic expression and deletion experiments indicates that Wor4 is positioned upstream of Wor1, and that it is formally an activator of the opaque cell type. The combination of ectopic expression and deletion phenotypes for Wor4 is unique; none of the other six white-opaque regulators show this pattern. We determined the pattern of Wor4 binding across the genome by ChIP-seq and found it is highly correlated with that of Wor1 and Wor2, indicating that Wor4 is tightly integrated into the existing white-opaque regulatory circuit. We previously proposed that white-to-opaque switching relies on the activation of a complex circuit of feedback loops that remains excited through many cell divisions. The identification of a new, central regulator of white-opaque switching supports this idea by indicating that the white-opaque switching mechanism is considerably more complex than those controlling conventional, nonheritable patterns of gene expression.
    Digitale ISSN: 2160-1836
    Thema: Biologie
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Publikationsdatum: 1986-06-01
    Beschreibung: The ordinary differential equation [formula omitted] which represents forced water waves on shallow water near resonance, is considered when the dispersion k is small. Asymptotic methods are used to show that there are multiple solutions with period 2π for a given value of the detuning parameter A. The effects of dissipation are also considered. © 1986, Cambridge University Press. All rights reserved.
    Print ISSN: 0022-1120
    Digitale ISSN: 1469-7645
    Thema: Maschinenbau , Physik
    Standort Signatur Erwartet Verfügbarkeit
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