<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Panas MW</submitter><funding>HHS | National Institutes of Health</funding><funding>Human Frontier Science Program</funding><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Science Foundation</funding><pagination>e00674-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6495377</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(2)</volume><pubmed_abstract>&lt;i>Toxoplasma gondii&lt;/i> is an obligate intracellular parasite that establishes a favorable environment in the host cells in which it replicates. We have previously reported that it uses MYR-dependent translocation of dense granule proteins to elicit a key set of host responses related to the cell cycle, specifically, E2F transcription factor targets, including cyclin E. We report here the identification of a novel &lt;i>Toxoplasma&lt;/i> effector protein that is exported from the parasitophorous vacuole in a MYR1-dependent manner and localizes to the host's nucleus. Parasites lacking this inducer of &lt;u>h&lt;/u>ost &lt;u>c&lt;/u>yclin &lt;u>E&lt;/u> (HCE1) are unable to modulate E2F transcription factor target genes and exhibit a substantial growth defect. Immunoprecipitation of HCE1 from infected host cells s</pubmed_abstract><journal>mBio</journal><pubmed_title>&lt;i>Toxoplasma&lt;/i> Controls Host Cyclin E Expression through the Use of a Novel MYR1-Dependent Effector Protein, HCE1.</pubmed_title><pmcid>PMC6495377</pmcid><funding_grant_id>R01 AI021423</funding_grant_id><funding_grant_id>P30 CA124435</funding_grant_id><funding_grant_id>RO1-AI021423</funding_grant_id><funding_grant_id>LT000404/2014-L</funding_grant_id><funding_grant_id>R01 AI129529</funding_grant_id><funding_grant_id>RO1-AI129529</funding_grant_id><funding_grant_id>DGE-114747</funding_grant_id><pubmed_authors>Panas MW</pubmed_authors><pubmed_authors>Naor A</pubmed_authors><pubmed_authors>Cygan AM</pubmed_authors><pubmed_authors>Boothroyd JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>Toxoplasma&lt;/i> Controls Host Cyclin E Expression through the Use of a Novel MYR1-Dependent Effector Protein, HCE1.</name><description>&lt;i>Toxoplasma gondii&lt;/i> is an obligate intracellular parasite that establishes a favorable environment in the host cells in which it replicates. We have previously reported that it uses MYR-dependent translocation of dense granule proteins to elicit a key set of host responses related to the cell cycle, specifically, E2F transcription factor targets, including cyclin E. We report here the identification of a novel &lt;i>Toxoplasma&lt;/i> effector protein that is exported from the parasitophorous vacuole in a MYR1-dependent manner and localizes to the host's nucleus. Parasites lacking this inducer of &lt;u>h&lt;/u>ost &lt;u>c&lt;/u>yclin &lt;u>E&lt;/u> (HCE1) are unable to modulate E2F transcription factor target genes and exhibit a substantial growth defect. Immunoprecipitation of HCE1 from infected host cells s</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2026-06-16T07:04:30.523Z</modification><creation>2019-06-06T23:10:28Z</creation></dates><accession>S-EPMC6495377</accession><cross_references><pubmed>31040242</pubmed><doi>10.1128/mBio.00674-19</doi></cross_references></HashMap>