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Series GSE161373 Query DataSets for GSE161373
Status Public on Mar 06, 2021
Title Yeast cell fate control by temporal redundancy modulation of transcription factor paralogs
Organisms Saccharomyces cerevisiae; Nakaseomyces glabratus
Experiment type Expression profiling by high throughput sequencing
Summary Recent single-cell studies have revealed that yeast stress response involves multiple transcription factors that are temporally activated in pulses. However, it remains largely unclear whether and how these dynamic transcription factors temporally interact to regulate stress survival. Here we show that budding yeast cells can exploit the temporal relationship between paralogous general stress regulators, Msn2 and Msn4, during stress response. We found that individual pulses of Msn2 and Msn4 are largely redundant, and cells can enhance the expression of their shared target genes by increasing their temporal divergence. Thus, functional redundancy between these two paralogs is modulated in a dynamic manner to confer fitness advantages for yeast cells, which might feed back to promote the preservation of their functional redundancy. This evolutionary implication was supported by evidence from Msn2/Msn4 orthologs and analyses of other transcription factor paralogs. Together, we show a cell fate control mechanism through temporal redundancy modulation in yeast, which may represent an evolutionarily important strategy for maintaining functional redundancy between gene duplicates.
 
Overall design First, for transient stimulation experiments, 7 genotypes (namely, 3 genotypes of S. cerevisiae: wild type sc, Msn2_sc deletion, Msn4_sc deletion and 4 genotypes of C. glabrata: wild type cg, Msn2_cg deletion, Msn4_cg deletion, Msn2_cg deletion Msn4_cg deletion) under two conditions (namely, stressed and control) were sequenced with 2 biological repeats. Second, for steady-state experiments, wild type sc strain was sequenced under 4 different carbon stresses with 2 biological repeats.
 
Contributor(s) Wu Y, Wu J, Deng M, Lin Y
Citation(s) 34035307
BioProject PRJNA675209
Submission date Nov 12, 2020
Last update date May 27, 2021
Contact name Yan WU
E-mail(s) wy-fcb@pku.edu.cn
Organization name Peking University
Department Academy for Advanced Interdisciplinary Studies
Lab Yihan Lin
Street address No.5 Yiheyuan Road Haidian District, Beijing, P.R.China
City Beijing
State/province Beijing
ZIP/Postal code 100871
Country China
 
Platforms (2)
GPL26171 HiSeq X Ten (Saccharomyces cerevisiae)
GPL29410 HiSeq X Ten ([Candida] glabrata)
Samples (36)
GSM4905558 Msn2_sc_deletion_0.5M_KCl_rep1
GSM4905559 Msn2_sc_deletion_control_rep1
GSM4905560 Msn4_sc_deletion_0.5M_KCl_rep1
Relations
SRA SRP291930

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
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Supplementary file Size Download File type/resource
GSE161373_cg_KCl_stress_rep1_featureCounts.csv.gz 171.4 Kb (ftp)(http) CSV
GSE161373_cg_KCl_stress_rep2_featureCounts.csv.gz 170.2 Kb (ftp)(http) CSV
GSE161373_sc_KCl_stress_rep1_fpkm.csv.gz 502.2 Kb (ftp)(http) CSV
GSE161373_sc_KCl_stress_rep2_fpkm.csv.gz 509.6 Kb (ftp)(http) CSV
GSE161373_sc_carbon_stress_rep1_fpkm.csv.gz 410.7 Kb (ftp)(http) CSV
GSE161373_sc_carbon_stress_rep2_fpkm.csv.gz 399.2 Kb (ftp)(http) CSV
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Processed data are available on Series record

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