<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(6)</volume><submitter>Hobert O</submitter><journal>Molecular and cellular biology</journal><pagination>3066-73</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC231301</full_dataset_link><abstract>The proto-oncogene product Vav plays a critical role in hematopoietic signal transduction. By using the yeast two-hybrid system, we identified a novel human protein, ENX-1, which interacts specifically with Vav both in vitro and in vivo. ENX-1 represents the human homolog of the Drosophila Enhancer of zeste gene, a member of the Polycomb group of genes, which are transcriptional regulators of homeobox gene expression. Interaction with ENX-1 suggests that Vav functions as an upstream element in the transcriptional regulation of homeobox genes, known to be important effectors in the hematopoietic system.</abstract><repository>biostudies-other</repository><pmcid>PMC231301</pmcid><data_source>Europe PMC</data_source><pubmed_authors>Hobert O</pubmed_authors><pubmed_authors>Ullrich A</pubmed_authors><pubmed_authors>Jallal B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interaction of Vav with ENX-1, a putative transcriptional regulator of homeobox gene expression.</name><description>The proto-oncogene product Vav plays a critical role in hematopoietic signal transduction. By using the yeast two-hybrid system, we identified a novel human protein, ENX-1, which interacts specifically with Vav both in vitro and in vivo. ENX-1 represents the human homolog of the Drosophila Enhancer of zeste gene, a member of the Polycomb group of genes, which are transcriptional regulators of homeobox gene expression. Interaction with ENX-1 suggests that Vav functions as an upstream element in the transcriptional regulation of homeobox genes, known to be important effectors in the hematopoietic system.</description><dates><release>1996-01-01T00:00:00Z</release><publication>1996 Jun</publication><modification>2019-03-27T00:35:52Z</modification><creation>2019-03-27T00:35:52Z</creation></dates><accession>S-EPMC231301</accession><cross_references><gen>U17564</gen><gen>U18007</gen><gen>U52965</gen><gen>U17552</gen><gen>U17563</gen><gen>U18003</gen><pubmed>8649418</pubmed><doi>10.1128/MCB.16.6.3066 </doi></cross_references></HashMap>