NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE61974 Query DataSets for GSE61974
Status Public on Oct 03, 2014
Title ChIP-seq analyses of the Aspergillus fumigatus SREBP SrbA
Organism Aspergillus fumigatus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary The Aspergillus fumigatus sterol regulatory element binding protein (SREBP) SrbA belongs to the basic Helix-Loop-Helix (bHLH) family of transcription factors and is crucial for antifungal drug resistance and virulence. The latter phenotype is especially striking, as loss of SrbA results in complete loss of virulence in murine models of invasive pulmonary aspergillosis (IPA). How fungal SREBPs mediate fungal virulence is unknown, though it has been suggested that lack of growth in hypoxic conditions accounts for the attenuated virulence. To further understand the role of SrbA in fungal infection site pathobiology, chromatin immunoprecipitation followed by massively parallel DNA sequencing (ChIP-seq) was used to identify genes under direct SrbA transcriptional regulation in hypoxia. These results confirmed the direct regulation of ergosterol biosynthesis and iron uptake by SrbA in hypoxia and revealed new roles for SrbA in nitrate assimilation and heme biosynthesis. Moreover, functional characterization of an SrbA target gene with sequence similarity to SrbA identified a new transcriptional regulator of the fungal hypoxia response and virulence, SrbB. SrbB co-regulates genes involved in heme biosynthesis and demethylation of C4 sterols with SrbA in hypoxic conditions. However, SrbB also has regulatory functions independent of SrbA including regulation of carbohydrate metabolism. Loss of SrbB markedly attenuates A. fumigatus virulence, and loss of both SREBPs further reduces in vivo fungal growth. These data suggest that both A. fumigatus SREBPs are critical for hypoxia adaptation and virulence and reveals new insights into SREBP’s complex role in infection site adaptation and fungal virulence.
 
Overall design 4 hour and 12 hour ChIP experiments were completed. Input control samples for each set were collected.
 
Contributor(s) Cramer RA, Carey CC, Barker BM
Citation(s) 25375670
Submission date Oct 02, 2014
Last update date May 15, 2019
Contact name Bridget Marie Barker
E-mail(s) [email protected]
Organization name TGEN-North
Department CFP
Lab Barker Lab
Street address 3051 Shamrell Blvd
City Flagstaff
State/province AZ
ZIP/Postal code 86001
Country USA
 
Platforms (1)
GPL18295 Illumina HiSeq 2000 (Aspergillus fumigatus)
Samples (6)
GSM1517809 WT_ChIP_RC12h.2011_11_30
GSM1517810 WT_ChIP_RC4H.2011_05_31
GSM1517811 WT_ChIP_RC4H.2011_11_11
Relations
BioProject PRJNA262849
SRA SRP048585

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE61974_combined.wt_chip.wt_id.fdr_0.05_peaks.txt.gz 4.4 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Processed data are available on Series record
Raw data are available in SRA

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap