<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Deng H</submitter><funding>NIDA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>3277-88</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4197530</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>141(16)</volume><pubmed_abstract>Interactions among transcription factors control their physiological functions by regulating their binding specificities and transcriptional activities. We implement a strategy to visualize directly the genomic loci that are bound by multi-protein complexes in single cells in Drosophila. This method is based on bimolecular fluorescence complementation (BiFC) analysis of protein interactions on polytene chromosomes. Drosophila Keap1 (dKeap1)-CncC complexes localized to the nucleus and bound chromatin loci that were not bound preferentially by dKeap1 or CncC when they were expressed separately. dKeap1 and CncC binding at these loci was enhanced by phenobarbital, but not by tert-butylhydroquinone (tBHQ) or paraquat. Endogenous dKeap1 and CncC activated transcription of the Jheh (Jheh1, Jheh2,</pubmed_abstract><journal>Development (Cambridge, England)</journal><pubmed_title>Visualization of the Drosophila dKeap1-CncC interaction on chromatin illumines cooperative, xenobiotic-specific gene activation.</pubmed_title><pmcid>PMC4197530</pmcid><funding_grant_id>R01 DA030339</funding_grant_id><funding_grant_id>P30 DK020572</funding_grant_id><funding_grant_id>R01 GM086213</funding_grant_id><funding_grant_id>GM086213</funding_grant_id><funding_grant_id>DA030339</funding_grant_id><pubmed_authors>Kerppola TK</pubmed_authors><pubmed_authors>Deng H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Visualization of the Drosophila dKeap1-CncC interaction on chromatin illumines cooperative, xenobiotic-specific gene activation.</name><description>Interactions among transcription factors control their physiological functions by regulating their binding specificities and transcriptional activities. We implement a strategy to visualize directly the genomic loci that are bound by multi-protein complexes in single cells in Drosophila. This method is based on bimolecular fluorescence complementation (BiFC) analysis of protein interactions on polytene chromosomes. Drosophila Keap1 (dKeap1)-CncC complexes localized to the nucleus and bound chromatin loci that were not bound preferentially by dKeap1 or CncC when they were expressed separately. dKeap1 and CncC binding at these loci was enhanced by phenobarbital, but not by tert-butylhydroquinone (tBHQ) or paraquat. Endogenous dKeap1 and CncC activated transcription of the Jheh (Jheh1, Jheh2,</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Aug</publication><modification>2025-05-29T20:27:13.941Z</modification><creation>2025-05-29T20:27:13.941Z</creation></dates><accession>S-EPMC4197530</accession><cross_references><pubmed>25063457</pubmed><doi>10.1242/dev.110528</doi></cross_references></HashMap>