Expression of seven members of the gene family encoding secretory aspartyl proteinases in Candida albicans

Details

Serval ID
serval:BIB_406E728AB537
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Expression of seven members of the gene family encoding secretory aspartyl proteinases in Candida albicans
Journal
Molecular Microbiology
Author(s)
Hube  B., Monod  M., Schofield  D. A., Brown  A. J., Gow  N. A.
ISSN
0950-382X (Print)
Publication state
Published
Issued date
10/1994
Volume
14
Number
1
Pages
87-99
Notes
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Oct
Abstract
The opportunistic fungal pathogen Candida albicans produces secretory aspartyl proteinases, which are believed to be virulence factors in infection. We have studied the in vitro expression of seven known members of the SAP gene family in a range of strains and serotypes by Northern analysis. SAP1 and SAP3 were regulated during phenotypic switching between the white and opaque forms of the organism. The SAP2 mRNA, which was the dominant transcript in the yeast form, was found to be autoinduced by peptide products of Sap2 activity and to be repressed by amino acids. The expression of the closely related SAP4-SAP6 genes was observed only at neutral pH during serum-induced yeast to hyphal transition. No SAP7 mRNA was detected under any of the conditions or in any of the strains tested. Our data suggest that the various members of the SAP gene family may have distinct roles in the colonization and invasion of the host.
Keywords
Amino Acid Sequence Aspartic Endopeptidases/*biosynthesis/genetics Blotting, Northern Candida albicans/*enzymology/*genetics/growth & development *Gene Expression Gene Expression Regulation, Enzymologic Gene Expression Regulation, Fungal *Genes, Fungal Hydrogen-Ion Concentration Kinetics Molecular Sequence Data *Multigene Family Phenotype RNA, Messenger/biosynthesis Transcription, Genetic
Pubmed
Web of science
Create date
25/01/2008 17:47
Last modification date
20/08/2019 14:38
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