Temperature-regulated transcription in the pathogenic fungus Cryptococcus neoformans

被引:75
作者
Steen, BR
Lian, T
Zuyderduyn, S
MacDonald, WK
Marra, M
Jones, SJM
Kronstad, JW [1 ]
机构
[1] Univ British Columbia, Dept Microbiol & Immunol, Biotechnol Lab, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Fac Agr Sci, Vancouver, BC V6T 1Z3, Canada
[3] British Columbia Canc Agcy, Genome Sci Ctr, Vancouver, BC V5Z 4E6, Canada
关键词
D O I
10.1101/gr.80202
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 basidiomycete fungus Cryptococcus neoformans is an opportunistic pathogen of worldwide importance that causes meningitis, leading to death in immunocompromised individuals. Unlike many basidiomycete fungi, C neoformans is thermotolerant, and its ability to grow at 37degreesC is considered to be a virulence factor. We used serial analysis of gene expression (SAGE) to characterize the transcriptomes of C neoformans strains that represent two varieties with different polysaccharide capsule serotypes. These include a serotype D strain of the C. neoformans variety neoformans and a serotype A strain of variety grubli. In this report, we describe the construction and characterization of SAGE libraries from each strain grown at 25degreesC and 37degreesC. The SAGE data reveal transcriptome differences between the two strains, even at this early stage of analysis, and identify sets of genes with higher transcript levels at 25degreesC or 37degreesC. Notably, growth at the lower temperature increased transcript levels for histone genes, indicating a general influence of temperature on chromatin structure. At 37degreesC, we noted elevated transcript levels for several genes encoding heat shock proteins and translation machinery. Some of these genes may play a role in temperature-regulated phenotypes in C neoformans, Such as the adaptation of the fungus to growth in the host and the dimorphic transition between budding and Filamentous growth. Overall, this work provides the most comprehensive gene expression data available for C neoformans; this information will be a critical resource both for gene discovery and genome annotation in this pathogen.
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页码:1386 / 1400
页数:15
相关论文
共 61 条
[21]   On the origins of congenic MATα and MATa strains of the pathogenic yeast Cryptococcus neoformans [J].
Heitman, J ;
Allen, B ;
Alspaugh, JA ;
Kwon-Chung, KJ .
FUNGAL GENETICS AND BIOLOGY, 1999, 28 (01) :1-5
[22]   RELATIONSHIP BETWEEN SUPEROXIDE-DISMUTASE AND MELANIN IN A PATHOGENIC FUNGUS [J].
JACOBSON, ES ;
JENKINS, ND ;
TODD, JM .
INFECTION AND IMMUNITY, 1994, 62 (09) :4085-4086
[23]   Changes in gene expression associated with developmental arrest and longevity in Caenorhabditis elegans [J].
Jones, SJM ;
Riddle, DL ;
Pouzyrev, AT ;
Velculescu, VE ;
Hillier, L ;
Eddy, SR ;
Stricklin, SL ;
Baillie, DL ;
Waterston, R ;
Marra, MA .
GENOME RESEARCH, 2001, 11 (08) :1346-1352
[24]  
Kakeya H, 1999, CLIN EXP IMMUNOL, V115, P485
[25]   A 77-kilodalton protein of Cryptococcus neoformans, a member of the heat shock protein 70 family, is a major antigen detected in the sera of mice with pulmonary Cryptococcosis [J].
Kakeya, H ;
Udono, H ;
Ikuno, N ;
Yamamoto, Y ;
Mitsutake, K ;
Miyazaki, T ;
Tomono, K ;
Koga, H ;
Tashiro, T ;
Nakayama, E ;
Kohno, S .
INFECTION AND IMMUNITY, 1997, 65 (05) :1653-1658
[26]   Two F-box/WD-repeat proteins Pop1 and Pop2 form hetero- and homo-complexes together with cullin-1 in the fission yeast SCF (Skp1-Cullin-1-F-box) ubiquitin ligase [J].
Kominami, K ;
Ochotorena, I ;
Toda, T .
GENES TO CELLS, 1998, 3 (11) :721-735
[27]  
Kwon-Chwag KJ, 1992, MED MYCOL, P397
[28]   ENCAPSULATION AND MELANIN FORMATION AS INDICATORS OF VIRULENCE IN CRYPTOCOCCUS-NEOFORMANS [J].
KWONCHUNG, KJ ;
RHODES, JC .
INFECTION AND IMMUNITY, 1986, 51 (01) :218-223
[29]   GENETIC ASSOCIATION OF MATING TYPES AND VIRULENCE IN CRYPTOCOCCUS-NEOFORMANS [J].
KWONCHUNG, KJ ;
EDMAN, JC ;
WICKES, BL .
INFECTION AND IMMUNITY, 1992, 60 (02) :602-605
[30]   Thermosensitive phenotype of yeast mutant lacking thioredoxin peroxidase [J].
Lee, SM ;
Park, JW .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 359 (01) :99-106