Skip to main content
. Author manuscript; available in PMC: 2018 May 1.
Published in final edited form as: Pharmacol Ther. 2017 Feb 4;173:135–145. doi: 10.1016/j.pharmthera.2017.02.012

Table 1.

TRB1 chip-seq studies

Reference Gronved, L. et al 2015 Ramadoss, P. et al 2014 Ayers, S. et al 2014 Chatonnet, F. et al 2013
Model mouse liver mouse liver cell culture cell culture
Detection method Monoclonal AB C1 biotin-streptavidin biotin-streptavidin biotin-streptavidin
Findings
DR4 is the most common TRE in positive targets
DR0 is associated with negative targets
T3 induced recruitment of TR to TRE
T3 independent interaction between TR and TRE
Majority of T3 binding sites found in intragenic regions
Little TRB binding sites near negative target genes
RXRalpha heterodimer partner Not done Not done Not done
TR isoform specific binding sites Not done Not done Not done
Motif enrichment analysis for TF other than TR
T3 regulated DNAase hypersensitive sites Not done Not done