<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(2)</volume><submitter>Blanco S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Cellular biological responses to specific stimulation are determined by a balance among signaling pathways. Protein interactions are likely to modulate these pathways. Vaccinia-related kinase-2 (VRK2) is a novel human kinase that can modulate different signaling pathways.&lt;h4>Principal findings&lt;/h4>We report that in vivo, the activity of JIP1-JNK complexes is downregulated by VRK2 in response to interleukin-1beta. Also the reduction of endogenous VRK2 with shRNA increases the transcriptional response to IL-1beta. The JIP1 scaffold protein assembles three consecutive members of a given MAPK pathway forming signaling complexes and their signal can be modulated by interactions with regulatory proteins that remain to be identified. Knocking-down JIP1 with siRNA resulted in el</pubmed_abstract><journal>PloS one</journal><pagination>e1660</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2243017</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Modulation of interleukin-1 transcriptional response by the interaction between VRK2 and the JIP1 scaffold protein.</pubmed_title><pmcid>PMC2243017</pmcid><pubmed_authors>Sanz-Garcia M</pubmed_authors><pubmed_authors>Santos CR</pubmed_authors><pubmed_authors>Blanco S</pubmed_authors><pubmed_authors>Lazo PA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Modulation of interleukin-1 transcriptional response by the interaction between VRK2 and the JIP1 scaffold protein.</name><description>&lt;h4>Background&lt;/h4>Cellular biological responses to specific stimulation are determined by a balance among signaling pathways. Protein interactions are likely to modulate these pathways. Vaccinia-related kinase-2 (VRK2) is a novel human kinase that can modulate different signaling pathways.&lt;h4>Principal findings&lt;/h4>We report that in vivo, the activity of JIP1-JNK complexes is downregulated by VRK2 in response to interleukin-1beta. Also the reduction of endogenous VRK2 with shRNA increases the transcriptional response to IL-1beta. The JIP1 scaffold protein assembles three consecutive members of a given MAPK pathway forming signaling complexes and their signal can be modulated by interactions with regulatory proteins that remain to be identified. Knocking-down JIP1 with siRNA resulted in el</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Feb</publication><modification>2025-04-04T14:11:28.904Z</modification><creation>2019-03-26T23:02:35Z</creation></dates><accession>S-EPMC2243017</accession><cross_references><pubmed>18286207</pubmed><doi>10.1371/journal.pone.0001660</doi></cross_references></HashMap>