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Series GSE148213 Query DataSets for GSE148213
Status Public on Feb 08, 2022
Title Transcriptome reprogramming of key transcription factor deletion strains of Saccharomyces cerevisiae compared with the wild type strain grown at normal temperature by RNA-Seq
Organism Saccharomyces cerevisiae
Experiment type Expression profiling by high throughput sequencing
Summary Saccharomyces cerevisiae cells have evolved remarkably sophisticated and flexible transcriptional regulatory networks (TRNs) that allow them to survive and thrive in stress conditions, such as high temperature, osmotic and oxidative conditions, etc. Furthermore, transcription factor plays a central role in transcriptional regulatory networks of stress response. To achieve a thorough understanding of master transcription factors and transcriptional regulatory networks in specific response to prolonged thermal stress, we previously sequenced mRNA from the cultures of the wild type strain ScY01a as well as three key transcription factor deletion strains including ScY01a (srb2∆), ScY01a (sin3∆) and ScY01a (mig1∆) grown at 40ºC in biological duplicates. Here, we further sequenced the corresponding samples cultured at 30ºC as a control. Differences in gene expression comparing the transcription factor deletion strains with the wild type strain by RNA deep sequencing revealed a hierarchical transcriptional regulatory network centered on these three transcription factors in S. cerevisiae.
 
Overall design mRNA levels in the wild type strain of Saccharomyces cerevisiae ScY01a as well as three key transcription factor deletion strains including ScY01a (srb2∆), ScY01a (sin3∆) and ScY01a (mig1∆) were examined by RNA Sequencing, in duplicate, using on Illumina platform using 150-bp paired-end sequencing. We sequenced 2 samples from ScY01a, 2 samples from ScY01a (srb2∆), 2 samples from ScY01a (sin3∆) and 2 samples from ScY01a (mig1∆), and identified differential expressions in the transcription factor deletion strain versus the wild type strain by using mRNA levels the wild type strain as a reference.
 
Contributor(s) Lin Y, Guo Y, Qi X, Gan Y, Wang Q
Citation(s) 35118059
Submission date Apr 07, 2020
Last update date Feb 08, 2022
Contact name Qinhong Wang
E-mail(s) wang_qh@tib.cas.cn
Organization name Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences
Lab Wang lab
Street address 32 West 7th Avenue, Tianjin Airport Economic Area
City Tianjin
ZIP/Postal code 300308
Country China
 
Platforms (1)
GPL27812 Illumina NovaSeq 6000 (Saccharomyces cerevisiae)
Samples (8)
GSM4456097 ScY01a-2
GSM4456098 ScY01a-3
GSM4456099 srb2-2
Relations
BioProject PRJNA623520
SRA SRP255577

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
GSE148213_Differential_gene_expression_mig1_vs._ScY01a.xlsx 42.2 Kb (ftp)(http) XLSX
GSE148213_Differential_gene_expression_sin3_vs._ScY01a.xlsx 422.1 Kb (ftp)(http) XLSX
GSE148213_Differential_gene_expression_srb2_vs._ScY01a.xlsx 425.7 Kb (ftp)(http) XLSX
GSE148213_Transcriptome_profiles_of_all_sequenced_strains.xlsx 546.7 Kb (ftp)(http) XLSX
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Processed data are available on Series record

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