<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee SH</submitter><funding>HHS | NIH | NIH Office of the Director</funding><funding>NSF | NSF Office of the Director</funding><funding>NIAID NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>9483-94</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5044833</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>90(20)</volume><pubmed_abstract>&lt;h4>Unlabelled&lt;/h4>The UL133-138 locus present in clinical strains of human cytomegalovirus (HCMV) encodes proteins required for latency and reactivation in CD34(+) hematopoietic progenitor cells and virion maturation in endothelial cells. The encoded proteins form multiple homo- and hetero-interactions and localize within secretory membranes. One of these genes, UL136 gene, is expressed as at least five different protein isoforms with overlapping and unique functions. Here we show that another gene from this locus, the UL138 gene, also generates more than one protein isoform. A long form of UL138 (pUL138-L) initiates translation from codon 1, possesses an amino-terminal signal sequence, and is a type one integral membrane protein. Here we identify a short protein isoform (pUL138-S) initia</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>Long and Short Isoforms of the Human Cytomegalovirus UL138 Protein Silence IE Transcription and Promote Latency.</pubmed_title><pmcid>PMC5044833</pmcid><funding_grant_id>T32 GM008692</funding_grant_id><funding_grant_id>R01 AI079059</funding_grant_id><funding_grant_id>T32 AI078985</funding_grant_id><funding_grant_id>AI079059</funding_grant_id><funding_grant_id>AI074984</funding_grant_id><funding_grant_id>R37 AI079059</funding_grant_id><funding_grant_id>R01 AI074984</funding_grant_id><pubmed_authors>Gelbmann CB</pubmed_authors><pubmed_authors>Goodrum F</pubmed_authors><pubmed_authors>Lee SH</pubmed_authors><pubmed_authors>Rak M</pubmed_authors><pubmed_authors>Caviness K</pubmed_authors><pubmed_authors>Kalejta RF</pubmed_authors><pubmed_authors>Albright ER</pubmed_authors><pubmed_authors>Lee JH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long and Short Isoforms of the Human Cytomegalovirus UL138 Protein Silence IE Transcription and Promote Latency.</name><description>&lt;h4>Unlabelled&lt;/h4>The UL133-138 locus present in clinical strains of human cytomegalovirus (HCMV) encodes proteins required for latency and reactivation in CD34(+) hematopoietic progenitor cells and virion maturation in endothelial cells. The encoded proteins form multiple homo- and hetero-interactions and localize within secretory membranes. One of these genes, UL136 gene, is expressed as at least five different protein isoforms with overlapping and unique functions. Here we show that another gene from this locus, the UL138 gene, also generates more than one protein isoform. A long form of UL138 (pUL138-L) initiates translation from codon 1, possesses an amino-terminal signal sequence, and is a type one integral membrane protein. Here we identify a short protein isoform (pUL138-S) initia</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2025-04-18T18:37:43.801Z</modification><creation>2019-03-27T02:25:36Z</creation></dates><accession>S-EPMC5044833</accession><cross_references><pubmed>27512069</pubmed><doi>10.1128/jvi.01547-16</doi><doi>10.1128/JVI.01547-16</doi></cross_references></HashMap>