NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE95807 Query DataSets for GSE95807
Status Public on Apr 11, 2017
Title Deciphering the Regulatory Network between the SREBP pathway and Protein Secretion in Neurospora crassa
Organism Neurospora crassa
Experiment type Expression profiling by high throughput sequencing
Summary Sterol Regulatory Element Binding Proteins (SREBPs) are conserved from yeast to mammalian cells and function in regulating sterol homeostasis. In fungi, the SREBP pathway has been implicated in the adaptation to hypoxia and in virulence. In Neurospora crassa and Trichoderma reesei, the SREBP pathway also negatively regulates protein secretion under lignocellulolytic conditions. Here we utilized global transcriptional profiling combined with genetic and physiological analyses to address the regulatory link between the SREBP pathway and protein secretion in N. crassa. Our results demonstrated that the function of the SREBP pathway in ergosterol biosynthesis and adaptation to hypoxia was conserved in N. crassa. Under lignocellulolytic conditions, the SREBP pathway was highly activated, resulting in the reduced expression of lytic polysaccharide monooxygenases, which require molecular oxygen for catalytic activity. Additionally, activation of the SREBP pathway under lignocellulolytic conditions repressed a set of genes predicted to be involved in the ER stress response. Here we show that the inability of a hac-1 mutant, which bears a deletion of the major regulator of the unfolded protein response (UPR), to efficiently produce cellulases and utilize cellulose was suppressed by mutations in the SREBP pathway. The analyses presented here demonstrated new functions of SREBP pathway, including linkages to the UPR and provide new clues for genetic engineering of filamentous fungi to improve their production of extracellular proteins.
 
Overall design Examination of mRNA levels of four strains WT, Δsah-2, Mclr-2 and Mclr-2Δsah-2 strains grown in sucrose minimal media for 24 hours after a shift from 16 hours in VMM by RNA -Seq. Each sample was set as three biological replicates.
 
Contributor(s) Qin L, Wu VW, Glass NL
Citation(s) 28420736
Submission date Mar 08, 2017
Last update date May 15, 2019
Contact name Lina Qin
E-mail(s) bioqinln@berkeley.edu
Phone 4156874329
Organization name University of Carlifornia
Street address 2151 Berkeley way
City Berkeley
State/province California
ZIP/Postal code 94720
Country USA
 
Platforms (1)
GPL23150 Illumina HiSeq 4000 (Neurospora crassa)
Samples (12)
GSM2526303 Wild type replicate 1
GSM2526304 Wild type replicate 2
GSM2526305 Wild type replicate 3
Relations
BioProject PRJNA378486
SRA SRP101555

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
GSE95807_RAW.tar 3.1 Mb (http)(custom) TAR (of FPKM_TRACKING)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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