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Status |
Public on Mar 26, 2018 |
Title |
ATAC-Seq analysis in vasopressin-responsive mouse renal collecting duct mpkCCD cells |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Vasopressin, a peptide hormone, controls renal water excretion, largely through regulation of water channel aquaporin-2 (AQP2) in the renal collecting duct. There are two regulatory mechanisms of AQP2: 1) short-term regulation by membrane trafficking of AQP2; and 2) long-term regulation involving vasopressin-induced changes of protein abundance of AQP2 through regulation of gene transcription and protein half-life. Vasopressin binds a G protein-coupled receptor (V2R) activating several downstream signaling pathways. At downstream of V2R activation, many of transcription factors involve gene transcription process associated with status of chromatin structure. ATAC-Seq (Assay for Transpoase-Accessible Chromatin using Sequencing) is a recent technique to study chromatin accessibility (Buenrostro et al. Nat Methods 2013). We carried out ATAC-Seq following standard an ATAC-Seq protocol in mpkCCD cells treated with vehicle or dDAVP for 30 minutes.
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Overall design |
To identify Tn5-accessible chromatin regions where transcription factors may bind, we carried out ATAC-seq . Observations were made both after 30 minutes treatment with the vasopressin analog dDAVP or vehicle (n=2 for each group).
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Contributor(s) |
Jung H, Knepper MA |
Citation(s) |
29572403 |
Submission date |
Jan 04, 2018 |
Last update date |
Feb 11, 2019 |
Contact name |
Hyun Jun Jung |
E-mail(s) |
hjung24@jhmi.edu
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Organization name |
Johns Hopkins University School of Medicine
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Department |
Medicine (Nephrology)
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Street address |
720 Rutland Ave, Ross Research Building 1165B
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City |
Baltimore |
State/province |
MD |
ZIP/Postal code |
21205 |
Country |
USA |
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Platforms (1) |
GPL21493 |
Illumina HiSeq 3000 (Mus musculus) |
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Samples (4)
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Relations |
BioProject |
PRJNA428530 |
SRA |
SRP130938 |