|
| Status |
Public on May 07, 2024 |
| Title |
ZNF143 binds DNA and stimulates transcription initiation to activate and repress direct target genes (PRO-seq) |
| Organism |
Homo sapiens |
| Experiment type |
Other
|
| Summary |
Transcription factors bind to sequence motifs and act as activators or repressors. Transcription factors interface with a constellation of accessory cofactors to regulate distinct mechanistic steps to regulate transcription. We rapidly degraded the essential and ubiquitously expressed transcription factor ZNF143 to determine its function in the transcription cycle. ZNF143 facilitates RNA Polymerase initiation and activates gene expression. ZNF143 binds the promoter of nearly all its activated target genes. Paradoxically, ZNF143 binds near the site of genic transcription initiation to directly repress a subset of genes. Although ZNF143 stimulates initiation at ZNF143-repressed genes (i.e. those that increase expression upon ZNF143 depletion), the molecular context of binding leads to cis repression. ZNF143 competes with other more efficient activators for promoter access, physically occludes transcription initiation sites, and acts as a molecular roadblock to RNA Polymerase to repress genes in cis. The term "context specific" is often invoked to describe transcription factors that have both activation and repression functions. Here, we define the context and molecular mechanisms of ZNF143-mediated cis activation and repression.
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| Overall design |
HEK293T cells with ZNF143 tagged with an inducible degron tag were treated with drugs to induce ZNF143 degradation for 30 minutes, then collected for PRO-seq.
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| Contributor(s) |
Dong J, Guertin MJ |
| Citation missing |
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| Submission date |
May 02, 2024 |
| Last update date |
May 07, 2024 |
| Contact name |
Jinhong Dong |
| E-mail(s) |
jdong@uchc.edu
|
| Organization name |
University of Connecticut
|
| Department |
Center for Cell Analysis and Modeling
|
| Street address |
400 Farmington Ave
|
| City |
Farmington |
| State/province |
CT |
| ZIP/Postal code |
06030 |
| Country |
USA |
| |
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| Platforms (1) |
|
| Samples (8)
|
| GSM8248130 |
HEK_CloneZD29_30min_control_PRO-seq rep1 |
| GSM8248131 |
HEK_CloneZD29_30min_control_PRO-seq rep2 |
| GSM8248132 |
HEK_CloneZD29_30min_control_PRO-seq rep3 |
| GSM8248133 |
HEK_CloneZD29_30min_control_PRO-seq rep4 |
| GSM8248134 |
HEK_CloneZD29_30min_dTAGV1_PRO-seq rep1 |
| GSM8248135 |
HEK_CloneZD29_30min_dTAGV1_PRO-seq rep2 |
| GSM8248136 |
HEK_CloneZD29_30min_dTAGV1_PRO-seq rep3 |
| GSM8248137 |
HEK_CloneZD29_30min_dTAGV1_PRO-seq rep4 |
|
| Relations |
| BioProject |
PRJNA1107334 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE266491_HEK_CloneZD29_30min_control_minus_PE1_scaled.bigWig |
175.2 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_control_minus_PE2_scaled.bigWig |
174.9 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_control_plus_PE1_scaled.bigWig |
181.8 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_control_plus_PE2_scaled.bigWig |
168.9 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_dTAGV1_minus_PE1_scaled.bigWig |
173.5 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_dTAGV1_minus_PE2_scaled.bigWig |
168.2 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_dTAGV1_plus_PE1_scaled.bigWig |
230.8 Mb |
(ftp)(http) |
BIGWIG |
| GSE266491_HEK_CloneZD29_30min_dTAGV1_plus_PE2_scaled.bigWig |
162.2 Mb |
(ftp)(http) |
BIGWIG |
SRA Run Selector |
| Raw data are available in SRA |
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