Affiliation:
1. Carlsberg Laboratory, Yeast Biology, Gamle Carlsberg Vej 10, DK-2500 Valby, Copenhagen, Denmark; Department of Microbiology, Friedrich-Schiller-University, Jena, Germany; and Junior Research Group, Fungal Pathogens, Leibniz Institute for Natural Product Research and Infection Biology—Hans-Knöll Institute, Jena, Beutenbergstr., 11a, D-07745 Jena, Germany
Abstract
ABSTRACT
Hyphal morphogenesis in
Candida albicans
is regulated by multiple pathways which act by either inducing or repressing filamentation. Most notably, Tup1, Nrg1, and Rfg1 are transcriptional repressors, while Efg1, Flo8, Cph1, and Czf1 can induce filamentation. Here, we present the functional analysis of Ca
SFL1
, which encodes the
C. albicans
homolog of the
Saccharomyces cerevisiae SFL1
(suppressor of flocculation) gene. Deletion of Ca
SFL1
results in flocculation (i.e., the formation of clumps) of yeast cells, which is most pronounced in minimal medium. The flocs contained hyphae already under noninducing conditions, and filamentation could be enhanced with hypha-inducing cues at 37°C. Expression of
SFL1
in a heterozygous mutant under the control of the Ca
MET3
promoter was shown to complement these defects and allowed switching between wild-type and mutant phenotypes. Interestingly, increased expression of
SFL1
using a
MET3prom-SFL1
construct prior to the induction of filamentation completely blocked germ tube formation. To localize Sfl1 in vivo, we generated a
SFL1-GFP
fusion. Sfl1-green fluorescent protein was found in the nucleus in both yeast cells and, to a lesser extent, hyphal cells. Using reverse transcription-PCR, we find an increased expression of
ALS1, ALS3, HWP1, ECE1
, and also
FLO8
. Our results suggest that Sfl1 functions in the repression of flocculation and filamentation and thus represents a novel negative regulator of
C. albicans
morphogenesis.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
55 articles.
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