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Status |
Public on Mar 12, 2014 |
Title |
Identification of beta-catenin binding regions in SW480 cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Deregulation of canonical Wnt/beta-catenin pathway is one of the earliest events in the pathogenesis of colon cancer. Mutations in APC or CTNNB1 (beta-catenin gene) are highly frequent in colon cancer and cause aberrant stabilization of b-catenin, which activates the transcription of Wnt target genes by binding to chromatin via the TCF/LEF transcription factors. Here we report an integrative analysis of genome-wide chromatin occupancy of b-catenin by chromatin immunoprecipitation coupled with high-throughput sequencing (ChIP-seq) and gene expression profiling by microarray analysis upon RNAi-mediated knockdown of beta-catenin in colon cancer cells (GSE53656).
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Overall design |
Immunoprecipitated samples from human colon cancer SW480 cells with antibodies against beta-catenin and control IgG respectively were used for ChIP-seq experiments.
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Contributor(s) |
Watanabe K, Dai X |
Citation(s) |
24651522 |
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Submission date |
Jan 08, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Kazuhide Watanabe |
E-mail(s) |
kazuhide.watanabe@riken.jp
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Phone |
+81-045-503-9222
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Organization name |
Riken
|
Department |
Center for Integrative Medical Sciences
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Street address |
1-7-22 Suehiro-cho Tsurumi-ku
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City |
Yokohama |
State/province |
Kanagawa |
ZIP/Postal code |
230-0045 |
Country |
Japan |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (2) |
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Relations |
BioProject |
PRJNA233973 |
SRA |
SRP035249 |