NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE234215 Query DataSets for GSE234215
Status Public on May 19, 2024
Title High Throughput Plant Activation Domain Identification and Mapping
Organism Saccharomyces cerevisiae
Experiment type Other
Summary Arabidopsis gene expression is regulated by more than 1,900 transcription factors (TFs), which have been identified genome-wide by the presence of well-conserved DNA binding domains. Activator TFs contain activation domains (ADs) that recruit coactivator complexes; however, for most Arabidopsis TFs, we lack knowledge about the presence, location, and transcriptional strength of their ADs. To address this gap, we experimentally identified Arabidopsis ADs on a proteome-wide scale, finding that over half of Arabidopsis TFs carry an AD. We annotated 1,553 ADs, the vast majority of which were previously unknown. We used the dataset generated to develop a neural network to accurately predict ADs and to identify sequence features necessary to recruit coactivator complexes. We uncovered six distinct sequence feature combinations that resulted in activation activity, providing a framework to interrogate activation domain sub-functionalization. Furthermore, we identified activation domains within the ancient AUXIN RESPONSE FACTOR (ARF) family of transcription factors, finding conservation of AD positioning in distinct clades. Our findings provide a deep resource for understanding transcriptional activation, a framework for examination of function within intrinsically disordered regions, and a predictive model of activation domains.
 
Overall design Arabidopsis TFs (PADI), or ARF regions (ARF Evolution and Pilot) were fragmented into 40 amino acid tiles with a 10 amino acid step size were made as oligo pools and cloned into plasmid libraries. Yeast transformations ensured integration of a single synthetic TF, each expressing one tile, at the URA3 locus. TF activity was induced with beta-estradiol and TF activity was measured using cell sorting based on the ratio of reporter to synthetic TF (GFP:mcherry). The distribution of tiles across GFP:mCherry ratio bins was determined with Next-generation sequencing of the integrated TF. Median GFP:mcherry values were used to calculate activation domain scores.
 
Contributor(s) Morffy N, Strader LC
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Jun 06, 2023
Last update date May 20, 2024
Contact name Lucia C. Strader
E-mail(s) lucia.strader@duke.edu
Organization name Duke University
Department Biology
Lab Strader Lab
Street address 124 Science Drive 3332 French Family Science Center
City Durham
State/province NC
ZIP/Postal code 27708
Country USA
 
Platforms (2)
GPL19756 Illumina NextSeq 500 (Saccharomyces cerevisiae)
GPL27812 Illumina NovaSeq 6000 (Saccharomyces cerevisiae)
Samples (164)
GSM7457346 PADI Library 10, Bin 10
GSM7457347 PADI Library 10, Bin 11
GSM7457348 PADI Library 10, Bin 12
Relations
BioProject PRJNA980550

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
GSE234215_RAW.tar 54.3 Mb (http)(custom) TAR (of CSV)
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