<HashMap><database>biostudies-literature</database><scores/><additional><submitter>McKerrow W</submitter><funding>NIA NIH HHS</funding><funding>IDeA</funding><funding>NIA</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><funding>NIGMS NIH HHS</funding><funding>NIGMS</funding><pagination>2033-2045</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10018344</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(5)</volume><pubmed_abstract>LINE-1 retrotransposons are sequences capable of copying themselves to new genomic loci via an RNA intermediate. New studies implicate LINE-1 in a range of diseases, especially in the context of aging, but without an accurate understanding of where and when LINE-1 is expressed, a full accounting of its role in health and disease is not possible. We therefore developed a method-5' scL1seq-that makes use of a widely available library preparation method (10x Genomics 5' single cell RNA-seq) to measure LINE-1 expression in tens of thousands of single cells. We recapitulated the known pattern of LINE-1 expression in tumors-present in cancer cells, absent from immune cells-and identified hitherto undescribed LINE-1 expression in human epithelial cells and mouse hippocampal neurons. In both cases, we saw a modest increase with age, supporting recent research connecting LINE-1 to age related diseases.</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>LINE-1 retrotransposon expression in cancerous, epithelial and neuronal cells revealed by 5' single-cell RNA-Seq.</pubmed_title><pmcid>PMC10018344</pmcid><funding_grant_id>R21 CA235521</funding_grant_id><funding_grant_id>P20 GM109035</funding_grant_id><funding_grant_id>P01 AG051449</funding_grant_id><funding_grant_id>R01 AG050582</funding_grant_id><funding_grant_id>HHSN261200800001E</funding_grant_id><funding_grant_id>P01AG051449</funding_grant_id><funding_grant_id>U24 CA210972</funding_grant_id><funding_grant_id>1R01AG050582-01A1</funding_grant_id><funding_grant_id>U24CA210972</funding_grant_id><funding_grant_id>P20GM109035</funding_grant_id><funding_grant_id>1R21CA235521</funding_grant_id><pubmed_authors>Evans SA</pubmed_authors><pubmed_authors>Sedivy JM</pubmed_authors><pubmed_authors>McKerrow W</pubmed_authors><pubmed_authors>Neretti N</pubmed_authors><pubmed_authors>Boeke JD</pubmed_authors><pubmed_authors>Kagermazova L</pubmed_authors><pubmed_authors>Frazzette N</pubmed_authors><pubmed_authors>Carucci J</pubmed_authors><pubmed_authors>Doudican N</pubmed_authors><pubmed_authors>Rocha A</pubmed_authors><pubmed_authors>Fenyo D</pubmed_authors><pubmed_authors>Kaparos EI</pubmed_authors></additional><is_claimable>false</is_claimable><name>LINE-1 retrotransposon expression in cancerous, epithelial and neuronal cells revealed by 5' single-cell RNA-Seq.</name><description>LINE-1 retrotransposons are sequences capable of copying themselves to new genomic loci via an RNA intermediate. New studies implicate LINE-1 in a range of diseases, especially in the context of aging, but without an accurate understanding of where and when LINE-1 is expressed, a full accounting of its role in health and disease is not possible. We therefore developed a method-5' scL1seq-that makes use of a widely available library preparation method (10x Genomics 5' single cell RNA-seq) to measure LINE-1 expression in tens of thousands of single cells. We recapitulated the known pattern of LINE-1 expression in tumors-present in cancer cells, absent from immune cells-and identified hitherto undescribed LINE-1 expression in human epithelial cells and mouse hippocampal neurons. In both cases, we saw a modest increase with age, supporting recent research connecting LINE-1 to age related diseases.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2024-10-15T05:11:58.538Z</modification><creation>2024-10-15T05:11:58.538Z</creation></dates><accession>S-EPMC10018344</accession><cross_references><pubmed>36744437</pubmed><doi>10.1093/nar/gkad049</doi></cross_references></HashMap>