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Eukaryot Cell ; 11(2): 141-50, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22140233

RESUMEN

We investigated the relevance of gene expression heterogeneity to virulence properties of a major fungal pathogen, Candida glabrata. The organism's key virulence-associated factors include glycosylphosphatidylinositol-anchored adhesins, encoded subtelomerically by the EPA gene family. Individual-cell analyses of expression revealed very striking heterogeneity for Epa1, an adhesin that mediates ∼95% of adherence to epithelial cells in vitro. The heterogeneity in Epa1 was markedly greater than that known for other yeast genes. Sorted cells expressing high or low levels of Epa1 exhibited high and low adherence to epithelial cells, indicating a link between gene expression noise and potential virulence. The phenotypes of sorted subpopulations reverted to mixed phenotypes within a few generations. Variation in single-cell Epa1 protein and mRNA levels was correlated, consistent with transcriptional regulation of heterogeneity. Sir-dependent transcriptional silencing was the primary mechanism driving heterogeneous Epa1 expression in C. glabrata BG2, but not in CBS138 (ATCC 2001). Inefficient silencing in the latter strain was not due to a difference in EPA1 sequence or (sub)telomere length and was overcome by ectopic SIR3 expression. Moreover, differences between strains in the silencing dependence of EPA1 expression were evident across a range of clinical isolates, with heterogeneity being the greatest in strains where EPA1 was subject to silencing. The study shows how heterogeneity can impact the virulence-related properties of C. glabrata cell populations, with potential implications for microbial pathogenesis more broadly.


Asunto(s)
Candida glabrata/genética , Candida glabrata/patogenicidad , Proteínas Fúngicas/genética , Regulación Fúngica de la Expresión Génica , Lectinas/genética , Candida glabrata/metabolismo , Adhesión Celular/genética , Células Epiteliales/metabolismo , Proteínas Fúngicas/metabolismo , Silenciador del Gen , Glicosilfosfatidilinositoles/metabolismo , Lectinas/metabolismo , Microscopía Fluorescente , Virulencia/genética
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