 |
 |
GEO help: Mouse over screen elements for information. |
|
| Status |
Public on Sep 04, 2010 |
| Title |
WT vs rim101 mutant gene expression under capsule inducing conditions |
| Platform organism |
Cryptococcus neoformans var. neoformans |
| Sample organism |
Cryptococcus neoformans var. grubii |
| Experiment type |
Expression profiling by array
|
| Summary |
Cryptococcus neoformans is a prevalent human fungal pathogen that must survive within various tissues in order to establish a human infection. We have identified the C. neoformans Rim101 transcription factor, a highly conserved pH-response regulator in many fungal species. The rim101- mutant strain displays growth defects similar to other fungal species in the presence of alkaline pH, increased salt concentrations, and iron limitation. However, the rim101- strain is also characterized by a striking defect in capsule, an important virulence-associated phenotype. This capsular defect is likely due to alterations in polysaccharide attachment to the cell surface, not in polysaccharide biosynthesis. In contrast to many other C. neoformans capsule-defective strains, the rim101- mutant is hypervirulent in animal models of cryptococcosis. Whereas Rim101 activation in other fungal species occurs through the conserved Rim pathway, we demonstrate that C. neoformans Rim101 is also activated by the cAMP/PKA pathway. We report here that C. neoformans uses PKA and the Rim pathway to regulate the localization, activation, and processing of the Rim101 transcription factor. We also demonstrate specific host- relevant activating conditions for Rim101 cleavage, showing that C. neoformans has co-opted conserved signaling pathways to respond to the specific niche within the infected host. These results establish a novel mechanism for Rim101 activation and the integration of two conserved signaling cascades in response to host environmental conditions.
|
| |
|
| Overall design |
WT and rim101 mutant total RNA isolated from yeast grown under capsule inducing conditions were compared in a dye-swap experiment. One culture of each representing a population of each strain were incubated in YPD culture medium to mid-logarithmic phase, then washed three times with sterile water before incubation in DMEM culture medium for 3 hours. Cells were washed three times before centrifugation and freezing on dry ice and lyophilizing.
|
| |
|
| Contributor(s) |
O'Meara TR, Norton D, Price MS, Hay C, Clements MF, Nichols CB, Alspaugh JA |
| Citation(s) |
20174553 |
| |
| Submission date |
Sep 01, 2010 |
| Last update date |
Mar 22, 2012 |
| Contact name |
Michael S Price |
| E-mail(s) |
msprice2@liberty.edu
|
| Phone |
434-592-7277
|
| Organization name |
Liberty University
|
| Department |
Biology & Chemistry
|
| Street address |
1971 University Blvd.
|
| City |
Lynchburg |
| State/province |
VA |
| ZIP/Postal code |
24515 |
| Country |
USA |
| |
|
| Platforms (1) |
| GPL4009 |
UBC/MSL C. neoformans serotype D 70K |
|
| Samples (1) |
| GSM589914 |
WT vs rim101 mutant gene expression |
|
| Relations |
| BioProject |
PRJNA130327 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE23929_RAW.tar |
3.3 Mb |
(http)(custom) |
TAR (of GPR) |
| Processed data included within Sample table |
|
|
|
|
 |
