<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang Y</submitter><funding>State Key Laboratory of Pathogen and Biosecurity</funding><funding>National Natural Science Foundation of China</funding><pagination>60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9861321</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;b>Background&lt;/b>: Endogenous retrovirus (ERV) elements can act as proximal regulatory elements in promoting interferon (IFN) responses. Previous relevant studies have mainly focused on IFN-stimulated genes (ISGs). However, the role of ERV elements as cis-regulatory motifs in regulating genes of the JAK-STAT pathway remains poorly understood. In our study, we analyzed the changes in ERV elements and genes under both IFN stimulation and blockade of the signaling pathway. &lt;b>Methods&lt;/b>: The effects of interferon on cells under normal conditions and knockout of the receptor were compared based on the THP1_IFNAR1_KO and THP1_IFNAR2_mutant cell lines. The correlation between differentially expressed ERVs (DHERVs) and differentially expressed genes (DEGs) as DEHERV-G pairs was explored with con</pubmed_abstract><journal>Viruses</journal><pubmed_title>Endogenous Retrovirus Elements Are Co-Expressed with IFN Stimulation Genes in the JAK-STAT Pathway.</pubmed_title><pmcid>PMC9861321</pmcid><funding_grant_id>31900157</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Han J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors><pubmed_authors>Jia L</pubmed_authors><pubmed_authors>Li L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Endogenous Retrovirus Elements Are Co-Expressed with IFN Stimulation Genes in the JAK-STAT Pathway.</name><description>&lt;b>Background&lt;/b>: Endogenous retrovirus (ERV) elements can act as proximal regulatory elements in promoting interferon (IFN) responses. Previous relevant studies have mainly focused on IFN-stimulated genes (ISGs). However, the role of ERV elements as cis-regulatory motifs in regulating genes of the JAK-STAT pathway remains poorly understood. In our study, we analyzed the changes in ERV elements and genes under both IFN stimulation and blockade of the signaling pathway. &lt;b>Methods&lt;/b>: The effects of interferon on cells under normal conditions and knockout of the receptor were compared based on the THP1_IFNAR1_KO and THP1_IFNAR2_mutant cell lines. The correlation between differentially expressed ERVs (DHERVs) and differentially expressed genes (DEGs) as DEHERV-G pairs was explored with con</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-06-23T03:26:05.048Z</modification><creation>2025-02-19T04:45:56.122Z</creation></dates><accession>S-EPMC9861321</accession><cross_references><pubmed>36680099</pubmed><doi>10.3390/v15010060</doi></cross_references></HashMap>