<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Knaupp AS</submitter><funding>ARC</funding><funding>State Government of Victoria</funding><funding>National Health and Medical Research Council</funding><funding>Australian Government</funding><funding>Australian Research Council</funding><pagination>1246-1259</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7724517</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(6)</volume><pubmed_abstract>Cellular identity is ultimately dictated by the interaction of transcription factors with regulatory elements (REs) to control gene expression. Advances in epigenome profiling techniques have significantly increased our understanding of cell-specific utilization of REs. However, it remains difficult to dissect the majority of factors that interact with these REs due to the lack of appropriate techniques. Therefore, we developed TINC: TALE-mediated isolation of nuclear chromatin. Using this new method, we interrogated the protein complex formed at the Nanog promoter in embryonic stem cells (ESCs) and identified many known and previously unknown interactors, including RCOR2. Further interrogation of the role of RCOR2 in ESCs revealed its involvement in the repression of lineage genes and the</pubmed_abstract><journal>Stem cell reports</journal><pubmed_title>TINC- A Method to Dissect Regulatory Complexes at Single-Locus Resolution- Reveals an Extensive Protein Complex at the Nanog Promoter.</pubmed_title><pmcid>PMC7724517</pmcid><funding_grant_id>CE140100008</funding_grant_id><funding_grant_id>APP1069830</funding_grant_id><funding_grant_id>APP1036587</funding_grant_id><funding_grant_id>APP1092280</funding_grant_id><funding_grant_id>GNT1178460</funding_grant_id><funding_grant_id>FT120100862</funding_grant_id><funding_grant_id>FT180100674</funding_grant_id><pubmed_authors>Lim SM</pubmed_authors><pubmed_authors>Polo JM</pubmed_authors><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>Ford E</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Nguyen T</pubmed_authors><pubmed_authors>Schroder J</pubmed_authors><pubmed_authors>Tripathi P</pubmed_authors><pubmed_authors>Mohenska M</pubmed_authors><pubmed_authors>Lister R</pubmed_authors><pubmed_authors>Holmes ML</pubmed_authors><pubmed_authors>Davidson KC</pubmed_authors><pubmed_authors>Larcombe MR</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Knaupp AS</pubmed_authors><pubmed_authors>Sun YBY</pubmed_authors><pubmed_authors>Nefzger CM</pubmed_authors><pubmed_authors>Haigh JJ</pubmed_authors><pubmed_authors>Schittenhelm RB</pubmed_authors><pubmed_authors>Wong K</pubmed_authors><pubmed_authors>Pflueger J</pubmed_authors><pubmed_authors>Firas J</pubmed_authors><pubmed_authors>Rossello FJ</pubmed_authors><pubmed_authors>Das PP</pubmed_authors></additional><is_claimable>false</is_claimable><name>TINC- A Method to Dissect Regulatory Complexes at Single-Locus Resolution- Reveals an Extensive Protein Complex at the Nanog Promoter.</name><description>Cellular identity is ultimately dictated by the interaction of transcription factors with regulatory elements (REs) to control gene expression. Advances in epigenome profiling techniques have significantly increased our understanding of cell-specific utilization of REs. However, it remains difficult to dissect the majority of factors that interact with these REs due to the lack of appropriate techniques. Therefore, we developed TINC: TALE-mediated isolation of nuclear chromatin. Using this new method, we interrogated the protein complex formed at the Nanog promoter in embryonic stem cells (ESCs) and identified many known and previously unknown interactors, including RCOR2. Further interrogation of the role of RCOR2 in ESCs revealed its involvement in the repression of lineage genes and the</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2026-05-03T04:06:34.986Z</modification><creation>2021-02-20T10:55:03Z</creation></dates><accession>S-EPMC7724517</accession><cross_references><pubmed>33296673</pubmed><doi>10.1016/j.stemcr.2020.11.005</doi></cross_references></HashMap>