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Status |
Public on May 01, 2010 |
Title |
Identification of Genes Preferentially Required for Growth of p53-Deficient Human Cancer Cells |
Organism |
Homo sapiens |
Experiment type |
Other
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Summary |
We describe a synthetic interaction screen to identify genes preferentially required for proliferation of p53-deficient human cancer cells. An isogenic pair of p53+/+ and p53-/- human colorectal HCT116 cell lines was stably transduced with a short hairpin RNA (shRNA) library encoded by lentiviruses that integrate in the genomic DNA of the host. Comparison of the frequency of each type of integrated lentivirus in the 2 cell types at an early time point (40hrs) and after about 12 mitotic cycles (10days), reveals genes whose knockdown preferentially impaired growth of p53-/- or p53+/+ HCT116 cells.
Keywords: Functional Genomics
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Overall design |
The region of the integrated lentiviruses is PCR amplified from genomic DNA of the two transduced cell populations at an early and a late time point.
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Contributor(s) |
Xie L, Gazin C, Zhu LJ, Debily M, Kittler EL, Zapp ML, Lapointe D, Gobeil S, Virbasius C, Green MR |
Citation(s) |
23284306 |
Submission date |
May 05, 2009 |
Last update date |
May 15, 2019 |
Contact name |
Michael R. Green |
E-mail(s) |
michael.green@umassmed.edu
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Organization name |
University of Massachusetts Medical School
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Department |
Molecular, Cell and Cancer Biology
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Lab |
Michael R. Green
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Street address |
364 Plantation Street
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City |
Worcester |
State/province |
MA |
ZIP/Postal code |
01605 |
Country |
USA |
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Platforms (1) |
GPL9052 |
Illumina Genome Analyzer (Homo sapiens) |
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Samples (4)
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Relations |
SRA |
SRP002515 |
BioProject |
PRJNA115543 |