<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang SY</submitter><funding>NIAID NIH HHS</funding><pagination>2919-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2118177</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>203(13)</volume><pubmed_abstract>It is thought that gene conversion (GCV) and somatic hypermutation (SHM) of immunoglobulin (Ig) genes occur in two steps: the generation of uracils in DNA by activation-induced cytidine deaminase, followed by their subsequent repair by various DNA repair pathways to generate sequence-diversified products. It is not known how either of the two steps is targeted specifically to Ig loci. Because of the tight link between transcription and SHM, we have investigated the role of endogenous Ig light chain (IgL) transcriptional control elements in GCV/SHM in the chicken B cell line DT40. Promoter substitution experiments led to identification of a strong RNA polymerase II promoter incapable of supporting efficient GCV/SHM. This surprising finding indicates that high levels of transcription are not</pubmed_abstract><journal>The Journal of experimental medicine</journal><pubmed_title>Control of gene conversion and somatic hypermutation by immunoglobulin promoter and enhancer sequences.</pubmed_title><pmcid>PMC2118177</pmcid><funding_grant_id>AI066130</funding_grant_id><funding_grant_id>R21 AI066130</funding_grant_id><pubmed_authors>Fugmann SD</pubmed_authors><pubmed_authors>Schatz DG</pubmed_authors><pubmed_authors>Yang SY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Control of gene conversion and somatic hypermutation by immunoglobulin promoter and enhancer sequences.</name><description>It is thought that gene conversion (GCV) and somatic hypermutation (SHM) of immunoglobulin (Ig) genes occur in two steps: the generation of uracils in DNA by activation-induced cytidine deaminase, followed by their subsequent repair by various DNA repair pathways to generate sequence-diversified products. It is not known how either of the two steps is targeted specifically to Ig loci. Because of the tight link between transcription and SHM, we have investigated the role of endogenous Ig light chain (IgL) transcriptional control elements in GCV/SHM in the chicken B cell line DT40. Promoter substitution experiments led to identification of a strong RNA polymerase II promoter incapable of supporting efficient GCV/SHM. This surprising finding indicates that high levels of transcription are not</description><dates><release>2006-01-01T00:00:00Z</release><publication>2006 Dec</publication><modification>2025-04-21T14:55:31.19Z</modification><creation>2019-03-26T23:28:22Z</creation></dates><accession>S-EPMC2118177</accession><cross_references><pubmed>17178919</pubmed><doi>10.1084/jem.20061835</doi></cross_references></HashMap>