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Status |
Public on May 05, 2023 |
Title |
The MMP-2 histone H3 N-terminal tail protease is selectively targeted to the transcription start sites of active genes [ChIP-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Our study examines the role of MMP-2 mediated Histone H3NT proteolysis in U2OS cells. We find binding of MMP-2 at all active protein coding transcription start sites, and examine the role it plays in local chromatin regulation and changes in gene expression.
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Overall design |
native ChIP-seq of 3XHA tagged Pro-MMP2 as well as a negative control (HA ChIP in WT cells not expressing tagged Pro-MMP2) and positive control (H3K4me3)
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Contributor(s) |
Weekley BH, Rice JC |
Citation(s) |
37161413 |
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Submission date |
Feb 08, 2023 |
Last update date |
Aug 07, 2023 |
Contact name |
Benjamin H Weekley |
E-mail(s) |
benjamin.weekley@mssm.edu
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Organization name |
Icahn School of Medicine at Mount Sinai
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Department |
Neuroscience
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Lab |
Maze Lab, Hess 9-201
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Street address |
1470 Madison Ave
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10029 |
Country |
USA |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE224887 |
The MMP-2 histone H3 N-terminal tail protease is selectively targeted to the transcription start sites of active genes |
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Relations |
BioProject |
PRJNA934553 |