<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>295(7)</volume><submitter>Zhang C</submitter><pubmed_abstract>The homeodomain protein NK2 homeobox 2 (NKX2-2) is a transcription factor that plays a critical role in the control of cell fate specification and differentiation in many tissues. In the developing central nervous system, this developmentally important transcription factor functions as a transcriptional repressor that governs oligodendrocyte (OL) differentiation and myelin gene expression, but the roles of various NKX2-2 structural domains in this process are unclear. In this study, using &lt;i>in situ&lt;/i> hybridization, immunofluorescence, and coimmunoprecipitation, we determined the structural domains that mediate the repressive functions of murine NKX2-2 and identified the transcriptional corepressors that interact with it in OL cells. Through &lt;i>in ovo&lt;/i> electroporation in embryonic chicken spinal cords, we demonstrate that the N-terminal Tinman domain and C-terminal domain synergistically promote OL differentiation by recruiting distinct transcriptional corepressors, including enhancer of split Groucho 3 (GRG3), histone deacetylase 1 (HDAC1), and DNA methyltransferase 3 ? (DNMT3A). We also observed that the NK2-specific domain suppresses the function of the C-terminal domain in OL differentiation. These findings delineate the distinct NKX2-2 domains and their roles in OL differentiation and suggest that NKX2-2 regulates differentiation by repressing gene expression via multiple cofactors and molecular mechanisms.</pubmed_abstract><journal>The Journal of biological chemistry</journal><pagination>1879-1888</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7029133</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The transcription factor NKX2-2 regulates oligodendrocyte differentiation through domain-specific interactions with transcriptional corepressors.</pubmed_title><pmcid>PMC7029133</pmcid><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Qiu M</pubmed_authors></additional><is_claimable>false</is_claimable><name>The transcription factor NKX2-2 regulates oligodendrocyte differentiation through domain-specific interactions with transcriptional corepressors.</name><description>The homeodomain protein NK2 homeobox 2 (NKX2-2) is a transcription factor that plays a critical role in the control of cell fate specification and differentiation in many tissues. In the developing central nervous system, this developmentally important transcription factor functions as a transcriptional repressor that governs oligodendrocyte (OL) differentiation and myelin gene expression, but the roles of various NKX2-2 structural domains in this process are unclear. In this study, using &lt;i>in situ&lt;/i> hybridization, immunofluorescence, and coimmunoprecipitation, we determined the structural domains that mediate the repressive functions of murine NKX2-2 and identified the transcriptional corepressors that interact with it in OL cells. Through &lt;i>in ovo&lt;/i> electroporation in embryonic chicken spinal cords, we demonstrate that the N-terminal Tinman domain and C-terminal domain synergistically promote OL differentiation by recruiting distinct transcriptional corepressors, including enhancer of split Groucho 3 (GRG3), histone deacetylase 1 (HDAC1), and DNA methyltransferase 3 ? (DNMT3A). We also observed that the NK2-specific domain suppresses the function of the C-terminal domain in OL differentiation. These findings delineate the distinct NKX2-2 domains and their roles in OL differentiation and suggest that NKX2-2 regulates differentiation by repressing gene expression via multiple cofactors and molecular mechanisms.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2021-02-21T09:27:36Z</modification><creation>2021-02-21T09:27:36Z</creation></dates><accession>S-EPMC7029133</accession><cross_references><pubmed>31932307</pubmed><doi>10.1074/jbc.ra119.011163</doi><doi>10.1074/jbc.RA119.011163</doi></cross_references></HashMap>