<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2</volume><submitter>Hashimoto M</submitter><pubmed_abstract>Protooncogene T-cell leukemia 1 (TCL1), which is implicated in human T-cell prolymphocytic leukemia (T-PLL), interacts with Akt and enhances its kinase activity, functioning as an Akt kinase co-activator. Two major isoforms of TCL1 Protooncogenes (TCL1 and TCL1b) are present adjacent to each other on human chromosome 14q.32. In human T-PLL, both TCL1 and TCL1b are activated by chromosomal translocation. Moreover, TCL1b-transgenic mice have never been created. Therefore, it remains unclear whether TCL1b itself, independent of TCL1, exhibits oncogenicity. In co-immunoprecipitation assays, both ectopic and endogenous TCL1b interacted with Akt. In in vitro Akt kinase assays, TCL1b enhanced Akt kinase activity in dose- and time-dependent manners. Bioinformatics approaches utilizing multiregress</pubmed_abstract><journal>Oncogenesis</journal><pagination>e70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3816220</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Protooncogene TCL1b functions as an Akt kinase co-activator that exhibits oncogenic potency in vivo.</pubmed_title><pmcid>PMC3816220</pmcid><pubmed_authors>Hirata N</pubmed_authors><pubmed_authors>Noguchi H</pubmed_authors><pubmed_authors>Tanaka S</pubmed_authors><pubmed_authors>Suizu F</pubmed_authors><pubmed_authors>Masuzawa M</pubmed_authors><pubmed_authors>Edamura T</pubmed_authors><pubmed_authors>Tokuyama W</pubmed_authors><pubmed_authors>Gotoh N</pubmed_authors><pubmed_authors>Hashimoto M</pubmed_authors><pubmed_authors>Matsuda-Lennikov M</pubmed_authors><pubmed_authors>Noguchi M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protooncogene TCL1b functions as an Akt kinase co-activator that exhibits oncogenic potency in vivo.</name><description>Protooncogene T-cell leukemia 1 (TCL1), which is implicated in human T-cell prolymphocytic leukemia (T-PLL), interacts with Akt and enhances its kinase activity, functioning as an Akt kinase co-activator. Two major isoforms of TCL1 Protooncogenes (TCL1 and TCL1b) are present adjacent to each other on human chromosome 14q.32. In human T-PLL, both TCL1 and TCL1b are activated by chromosomal translocation. Moreover, TCL1b-transgenic mice have never been created. Therefore, it remains unclear whether TCL1b itself, independent of TCL1, exhibits oncogenicity. In co-immunoprecipitation assays, both ectopic and endogenous TCL1b interacted with Akt. In in vitro Akt kinase assays, TCL1b enhanced Akt kinase activity in dose- and time-dependent manners. Bioinformatics approaches utilizing multiregress</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Sep</publication><modification>2025-04-22T16:31:39.939Z</modification><creation>2019-03-27T01:18:03Z</creation></dates><accession>S-EPMC3816220</accession><cross_references><pubmed>24042734</pubmed><doi>10.1038/oncsis.2013.30</doi></cross_references></HashMap>