MULTIPLICITY OF GENES ENCODING SECRETED ASPARTIC PROTEINASES IN CANDIDA SPECIES

被引:202
作者
MONOD, M
TOGNI, G
HUBE, B
SANGLARD, D
机构
[1] UNIV ABERDEEN, MARISCHAL COLL, DEPT MOLEC & CELL BIOL, ABERDEEN AB9 1AS, SCOTLAND
[2] ETH ZURICH, INST BIOTECHNOL, CH-8093 ZURICH, SWITZERLAND
[3] CHU VAUDOIS, INST MICROBIOL, CH-1011 LAUSANNE, SWITZERLAND
关键词
D O I
10.1111/j.1365-2958.1994.tb00429.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The secreted aspartic proteinases (SAP) of Candida sp. are presumed to be potential virulence factors. In the opportunistic pathogen Candida albicans the proteinase genes identified to date, SAP1, SAP2, SAP3 and SAP4, constitute a multigene family. Before addressing the possible role of each proteinase in virulence, we sought to isolate all the members of this multigene family by screening a genomic library with a SAP1 probe for additional C. albicans SAP genes using low-stringency hybridization conditions. Three putative new members, SAP5, SAP6 and SAP7 were isolated and sequenced. The N-terminal segments of the deduced amino acid sequences of SAPS and SAPS contained secretion signal sequences similar to those of other Candida SAPs. Upon comparison and alignment with the other reported SAP amino acid sequences, SAP7 is not only the most divergent protein but also exhibits a much longer putative prosequence with a single Lys-Lys putative processing site. Using SAP1 to SAP7 as probes, the overall number of SAP genes in C.albicans was tentatively estimated by low-stringency hybridization to EcoRl-digested genomic DNA. While each isolated SAP gene could be assigned to distinct EcoRl bands, the existence of two additional genes not isolated after screening of the C.albicans gene library was inferred. Furthermore, evidence was obtained for the existence of SAP multigene families in other Candida species such as C. tropicalis, C. parapsilosis and C. guillermondii.
引用
收藏
页码:357 / 368
页数:12
相关论文
共 51 条
[41]  
RUCHEL R, 1986, INFECT IMMUN, V53, P411
[42]   PROPERTIES OF A PURIFIED PROTEINASE FROM THE YEAST CANDIDA-ALBICANS [J].
RUCHEL, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 659 (01) :99-113
[43]  
Sambrook J., 1989, MOL CLONING LAB MANU
[44]  
SANGLARD D, 1992, FEMS MICROBIOL LETT, V95, P149, DOI 10.1111/j.1574-6968.1992.tb05358.x
[45]   IDENTIFICATION AND CHARACTERIZATION OF ADDITIONAL MEMBERS OF THE CYTOCHROME-P450 MULTIGENE FAMILY CYP52 OF CANDIDA-TROPICALIS [J].
SEGHEZZI, W ;
MEILI, C ;
RUFFINER, R ;
KUENZI, R ;
SANGLARD, D ;
FIECHTER, A .
DNA AND CELL BIOLOGY, 1992, 11 (10) :767-780
[46]   ISOLATION AND NUCLEOTIDE-SEQUENCE OF THE EXTRACELLULAR ACID PROTEASE GENE (ACP) FROM THE YEAST CANDIDA-TROPICALIS [J].
TOGNI, G ;
SANGLARD, D ;
FALCHETTO, R ;
MONOD, M .
FEBS LETTERS, 1991, 286 (1-2) :181-185
[47]  
TOGNI G, 1994, IN PRESS J MED VET M, V32
[48]   A NEW METHOD FOR PREDICTING SIGNAL SEQUENCE CLEAVAGE SITES [J].
VONHEIJNE, G .
NUCLEIC ACIDS RESEARCH, 1986, 14 (11) :4683-4690
[49]   3 DISTINCT SECRETED ASPARTYL PROTEINASES IN CANDIDA-ALBICANS [J].
WHITE, TC ;
MIYASAKI, SH ;
AGABIAN, N .
JOURNAL OF BACTERIOLOGY, 1993, 175 (19) :6126-6133
[50]   PHYSICAL AND GENETIC-MAPPING OF CANDIDA-ALBICANS - SEVERAL GENES PREVIOUSLY ASSIGNED TO CHROMOSOME-1 MAP TO CHROMOSOME-R, THE RDNA-CONTAINING LINKAGE GROUP [J].
WICKES, B ;
STAUDINGER, J ;
MAGEE, BB ;
KWONCHUNG, KJ ;
MAGEE, PT ;
SCHERER, S .
INFECTION AND IMMUNITY, 1991, 59 (07) :2480-2484