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
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.
引用
收藏
页码:263 / 271
页数:9
相关论文
共 53 条
  • [1] COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT
    ADAMS, MD
    KELLEY, JM
    GOCAYNE, JD
    DUBNICK, M
    POLYMEROPOULOS, MH
    XIAO, H
    MERRIL, CR
    WU, A
    OLDE, B
    MORENO, RF
    KERLAVAGE, AR
    MCCOMBIE, WR
    VENTER, JC
    [J]. SCIENCE, 1991, 252 (5013) : 1651 - 1656
  • [2] Cellular immune responses to recombinant heat shock protein 70 from Histoplasma capsulatum
    Allendoerfer, R
    Maresca, B
    Deepe, GS
    [J]. INFECTION AND IMMUNITY, 1996, 64 (10) : 4123 - 4128
  • [3] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [4] Large-scale comparison of fungal sequence information:: Mechanisms of innovation in neurospora crassa and gene loss in Saccharomyces cerevisiae
    Braun, EL
    Halpern, AL
    Nelson, MA
    Natvig, DO
    [J]. GENOME RESEARCH, 2000, 10 (04) : 416 - 430
  • [5] Electrophoretic karyotypes and genome sizing of the pathogenic fungus Paracoccidioides brasiliensis
    Cano, MIN
    Cisalpino, PS
    Galindo, I
    Ramírez, JL
    Mortara, RA
    da Silveira, JF
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) : 742 - 747
  • [6] Genomic Exploration of the Hemiascomycetous Yeasts:: 17.: Yarrowia lipolytica
    Casaregola, S
    Neuvéglise, C
    Lépingle, A
    Bon, E
    Feynerol, C
    Artiguenave, F
    Wincker, P
    Gaillardin, C
    [J]. FEBS LETTERS, 2000, 487 (01) : 95 - 100
  • [7] Characterization of a gene which encodes a mannosyltransferase homolog of Paracoccidioides brasiliensis
    Costa, AA
    Gómez, FJ
    Pereira, M
    Felipe, MSS
    Jesuino, RSA
    Deepe, GS
    Soares, CMA
    [J]. MICROBES AND INFECTION, 2002, 4 (10) : 1027 - 1034
  • [8] Identification, N-terminal region sequencing and similarity analysis of differentially expressed proteins in Paracoccidioides brasiliensis
    Cunha, AF
    Sousa, MV
    Silva, SP
    Jesuíno, RSA
    Soares, CMA
    Felipe, MSS
    [J]. MEDICAL MYCOLOGY, 1999, 37 (02) : 115 - 121
  • [9] Heterologous expression, purification, and immunological reactivity of a recombinant HSP60 from Paracoccidioides brasiliensis
    Cunha, DA
    Zancopé-Oliveira, RM
    Felipe, MSS
    Salem-Izacc, SM
    Deepe, GS
    Soares, CMA
    [J]. CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2002, 9 (02) : 374 - 377
  • [10] Differential expression of an hsp70 gene during transition from the mycelial to the infective yeast form of the human pathogenic fungus Paracoccidioides brasiliensis
    da Silva, SP
    Borges-Walmsley, MI
    Pereira, IS
    Soares, CMD
    Walmsley, AR
    Felipe, MSS
    [J]. MOLECULAR MICROBIOLOGY, 1999, 31 (04) : 1039 - 1050