Multiomic Analysis of the UV-Induced DNA Damage Response
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Boeing-2016-Multiomic Analysis o.pdf
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Checksum (MD5)
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Author(s)
Boeing, Stefan
Williamson, Laura
Encheva, Vesela
Gori, Ilaria
Saunders, Rebecca E.
Instrell, Rachael
Rodriguez-Martinez, Marta
Weems, Juston C.
Kelly, Gavin P.
Conaway, Joan W.
Date Issued
May 2016
Journal
Cell Reports
Publisher
Elsevier
Citation
Boeing, Stefan, Laura Williamson, Vesela Encheva, Ilaria Gori, Rebecca E. Saunders, Rachael Instrell, Ozan Aygün, et al. “Multiomic Analysis of the UV-Induced DNA Damage Response.” Cell Reports 15, no. 7 (May 2016): 1597–1610.
Version
Final published version
Abstract
In order to facilitate the identification of factors and pathways in the cellular response to UV-induced DNA damage, several descriptive proteomic screens and a functional genomics screen were performed in parallel. Numerous factors could be identified with high confidence when the screen results were superimposed and interpreted together, incorporating biological knowledge. A searchable database, bioLOGIC, which provides access to relevant information about a protein or process of interest, was established to host the results and facilitate data mining. Besides uncovering roles in the DNA damage response for numerous proteins and complexes, including Integrator, Cohesin, PHF3, ASC-1, SCAF4, SCAF8, and SCAF11, we uncovered a role for the poorly studied, melanoma-associated serine/threonine kinase 19 (STK19). Besides effectively uncovering relevant factors, the multiomic approach also provides a systems-wide overview of the diverse cellular processes connected to the transcription-related DNA damage response.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Terms of Use
Creative Commons Attribution 4.0 International License
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DOI of Published Version
https://doi.org/10.1016/j.celrep.2016.04.047
