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Transcriptome characterization of the dimorphic and pathogenic fungus Paracoccidioides brasiliensis by EST analysis
被引:75
作者:
Felipe, MSS
[1
]
Andrade, RV
Petrofeza, SS
Maranhao, AQ
Torres, FAG
Albuquerque, P
Arraes, FBM
Arruda, M
Azevedo, MO
Baptista, AJ
Bataus, LAM
Borges, CL
Campos, EG
Cruz, MR
Daher, BS
Dantas, A
Ferreira, MASV
Ghil, GV
Jesuino, RSA
Kyaw, CM
Leitao, L
Martins, CR
Moraes, LMP
Neves, EO
Nicola, AM
Alves, ES
Parente, JA
Pereira, M
Poças-Fonseca, MJ
Resende, R
Ribeiro, BM
Saldanha, RR
Santos, SC
Silva-Pereira, I
Silva, MAS
Silveira, E
Simoes, IC
Soares, RBA
Souza, DP
De-Souza, MT
Andrade, EV
Xavier, MAS
Veiga, HP
Venancio, EJ
Carvalho, MJA
Oliveira, AG
Inoue, MK
Almeida, NF
Walter, MEMT
Soares, CMA
机构:
[1] Univ Brasilia, Mol Biol Lab, Inst Ciencias Biol, BR-70910900 Brasilia, DF, Brazil
[2] Univ Brasilia, Dept Gencia Computac, BR-70910900 Brasilia, DF, Brazil
[3] Univ Fed Goias, Inst Ciencias Biol, Mol Biol Lab, BR-74001970 Goiania, Go, Brazil
[4] Univ Estadual Londrina, Ctr Ciencias Biol, Dept Ciencias Patol, BR-86051970 Londrina, PR, Brazil
[5] Univ Fed Mato Grosso do Sul, Ctr Ciencias Exatas & Tecnol, Dept Computac & Estat, BR-79070900 Campo Grande, MS, Brazil
[6] Univ Fed Mato Grosso do Sul, Ctr Ciencias Nat & Tecnol, Dept Ciencias Biol, BR-78200000 Caceres, MT, Brazil
来源:
关键词:
ESTs;
transcriptome;
functional genomics;
human pathogenic fungus;
dimorphism;
Paracoccidioides brasiliensis;
D O I:
10.1002/yea.964
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:
Paracoccidioides brasiliensis is a pathogenic fungus that undergoes a temperature-dependent cell morphology change from mycelium (22degreesC) to yeast (36degreesC). It is assumed that this morphological transition correlates with the infection of the human host. Our goal was to identify genes expressed in the mycelium (M) and yeast (Y) forms by EST sequencing in order to generate a partial map of the fungus transcriptome. Individual EST sequences were clustered by the CAP3 program and annotated using Blastx similarity analysis and InterPro Scan. Three different databases, GenBank nr, COG (clusters of orthologous groups) and GO (gene ontology) were used for annotation. A total of 3938 (Y = 1654 and M = 2274) ESTs were sequenced and clustered into 597 contigs and 1563 singlets, making up a total of 2160 genes, which possibly represent one-quarter of the complete gene repertoire in P. brasiliensis. From this total, 1040 were successfully annotated-and 894 could be classified in 18 functional COG categories as follows: cellular metabolism (44%); information storage and processing (25%); cellular processes - cell division, posttranslational modifications, among others (19 %); and genes of unknown functions (12%). Computer analysis enabled us to identify some genes potentially involved in the dimorphic transition and drug resistance. Furthermore, computer subtraction analysis revealed several genes possibly expressed in stage-specific forms of P. brasiliensis. Further analysis of these genes may provide new insights into the pathology and differentiation of P. brasiliensis. All EST sequences have been deposited in GenBank under Accession Nos CA580326-CA584263. Copyright (C) 2003 John Wiley Sons, Ltd.
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页码:263 / 271
页数:9
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