Research Article
A Cell Model for Conditional Profiling of Androgen-Receptor-Interacting Proteins
Table 3
Top half: gene lists representing the BIOCARTA pathways “telomeres, telomerase, cellular aging, and immortality”, “chromatin remodeling by hSWI/SNF ATP-dependent complexes” and “control of gene expression by vitamin D receptor” found to be overrepresented among the known AR-interacting proteins identified in the N-TAP purifications by the bioinformatics tool DAVID. Bottom half: gene lists representing the “Kegg pathway” “pathways in cancer”, and “prostate cancer” identified as being overrepresented among the known AR-interacting proteins identified in the N-TAP purifications by the bioinformatics tool “DAVID” and “g-profiler”. Listed are the interacting proteins that were unique for the proliferating cells (33), interacting proteins that were unique for the nonproliferating cells (37), and interacting proteins common to both (common). The AR is bolded.
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