Transcriptional Activation Domains of the Candida albicans Gcn4p and Gal4p Homologs

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DOIResolve DOI: http://doi.org/10.1128/EC.00183-06
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TypeArticle
Journal titleEukaryotic Cell
Volume6
Issue2
Pages291301; # of pages: 11
Subjectanalysis; Candida; Candida albicans; Dna; genome; Leucine; pha; Protein; Proteins; Saccharomyces cerevisiae; Transcription Factors; Yeast; Zinc
AbstractMany putative transcription factors in the pathogenic fungus Candida albicans contain sequence similarity to well-defined transcriptional regulators in the budding yeast Saccharomyces cerevisiae, but this sequence similarity is often limited to the DNA binding domains of the molecules. The Gcn4p and Gal4p proteins of Saccharomyces cerevisiae are highly studied and well-understood eukaryotic transcription factors of the basic leucine zipper (Gcn4p) and C6 zinc cluster (Gal4p) families; C. albicans has C. albicans Gcn4p (CaGcn4p) and CaGal4p with DNA binding domains highly similar to their S. cerevisiae counterparts. Deletion analysis of the CaGcn4p protein shows that the N' terminus is needed for transcriptional activation; an 81-amino-acid region is critical for this function, and this domain can be coupled to a lexA DNA binding module to provide transcription-activating function in a heterologous reporter system. Deletion analysis of the C. albicans Gal4p identifies a C-terminal 73-amino-acid-long transcription-activating domain that also can be transferred to a heterologous reporter construct to direct transcriptional activation. These two transcriptional activation regions show no sequence similarity to the respective domains in their S. cerevisiae homologs, and the two C. albicans transcription-activating domains themselves show little similarity.
Publication date
LanguageEnglish
AffiliationNRC Biotechnology Research Institute; National Research Council Canada
Peer reviewedNo
NRC number47514
NPARC number3539731
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Record identifier3e312f36-484e-4364-ac41-12e508c41a63
Record created2009-03-01
Record modified2016-05-09
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