The histone deacetylase genes HDA1 and RPD3 play distinct roles in regulation of high-frequency phenotypic switching in Candida albicans

被引:102
作者
Srikantha, T
Tsai, L
Daniels, K
Klar, AJS
Soll, DR [1 ]
机构
[1] Univ Iowa, Dept Sci Biol, Iowa City, IA 52242 USA
[2] NCI, Frederick Canc Res & Dev Ctr, Dev Genet Sect, Gene Regulat & Chromosome Biol Lab, Frederick, MD 21702 USA
关键词
D O I
10.1128/JB.183.15.4614-4625.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Five histone deacetylase genes (HDA1, RPD3, HOS1, HOS2, and HOS3) have been cloned from Candida albicans and characterized. Sequence analysis and comparison with 17 additional deacetylases resulted in a phylogenetic tree composed of three major groups. Transcription of the deacetylases HDA1 and RPD3 is downregulated in the opaque phase of the white-opaque transition in strain WO-1, HOS3 is selectively transcribed as a 2.5-kb transcript in the white phase and as a less-abundant 2.3-kb transcript in the opaque phase, HD:II and RPD3 were independently deleted in strain WO-1, and both switching between the white and opaque phases and the downstream regulation of phase-specific genes were analyzed. Deletion of HDA1 resulted in an increase in the frequency of switching from the white phase to the opaque phase, but had no effect on the frequency of switching from the opaque phase to the white phase. Deletion of RPD3 resulted in an increase in the frequency of switching in both directions. Deletion of HDAI resulted in reduced white-phase-specific expression of the EFG1 3.2-kb transcript, but had no significant effect on white-phase-specific expression of WH11 or opaque-phase-specific expression of OP4, SAP1, and SAP3. Deletion of RPD3 resulted in reduced opaque-phase-specific expression of OP4 SAP1, and SAP3 and a slight reduction of white-phase-specific expression of WH11 and 3.2-kb EFG1. Deletion of neither HDAI nor RPD3 affected the high level of white-phase expression and the low level of opaque-phase expression of the MADS box protein gene MCM1, which has been implicated in the regulation of opaque-phase-specific gene expression. In addition, there was no effect on the phase-regulated levels of expression of the other deacetylase genes. These results demonstrate that the two, deacetylase genes HDA1 and RPD3 play distinct roles in the suppression of switching, that the two play distinct and selective roles in the regulation of phase-specific genes, and that the deacetylases are in turn regulated by switching.
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页码:4614 / 4625
页数:12
相关论文
共 65 条
[1]   UNIQUE PHENOTYPE OF OPAQUE CELLS IN THE WHITE-OPAQUE TRANSITION OF CANDIDA-ALBICANS [J].
ANDERSON, JM ;
SOLL, DR .
JOURNAL OF BACTERIOLOGY, 1987, 169 (12) :5579-5588
[2]   Histone deacetylases: transcriptional repression with SINers and NuRDs [J].
Ayer, DE .
TRENDS IN CELL BIOLOGY, 1999, 9 (05) :193-198
[3]   The Candida albicans CDR3 gene codes for an opaque-phase ABC transporter [J].
Balan, I ;
Alarco, AM ;
Raymond, M .
JOURNAL OF BACTERIOLOGY, 1997, 179 (23) :7210-7218
[4]   EFFECTS OF LOW CONCENTRATIONS OF ZINC ON THE GROWTH AND DIMORPHISM OF CANDIDA-ALBICANS - EVIDENCE FOR ZINC-RESISTANT AND ZINC-SENSITIVE PATHWAYS FOR MYCELIUM FORMATION [J].
BEDELL, GW ;
SOLL, DR .
INFECTION AND IMMUNITY, 1979, 26 (01) :348-354
[5]   Genomewide studies of histone deacetylase function in yeast [J].
Bernstein, BE ;
Tong, JK ;
Schreiber, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13708-13713
[6]   Control of filament formation in Candida albicans by the transcriptional repressor TUP1 [J].
Braun, BR ;
Johnson, AD .
SCIENCE, 1997, 277 (5322) :105-109
[7]   HDA1 and HDA3 are components of a yeast histone deacetylase (HDA) complex [J].
Carmen, AA ;
Rundlett, SE ;
Grunstein, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (26) :15837-15844
[8]  
DAYHOFF MO, 1979, ATLAS PROTEIN SEQUEN
[9]  
DeRubertis F, 1996, NATURE, V384, P589
[10]   Transient inhibition of histone deacetylation alters the structural and functional imprint at fission yeast centromeres [J].
Ekwall, K ;
Olsson, T ;
Turner, BM ;
Cranston, G ;
Allshire, RC .
CELL, 1997, 91 (07) :1021-1032