<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jeon BC</submitter><funding>National Research Foundation of Korea (NRF)</funding><funding>Korea Research Institute of Bioscience and Biotechnology (KRIBB)</funding><funding>National Research Council of Science and Technology (National Research Council of Science &amp; Technology)</funding><pagination>68-82</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11686140</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>V(D)J recombination secures the production of functional immunoglobulin (Ig) genes and antibody diversity during the early stages of B-cell development through long-distance interactions mediated by cis-regulatory elements and trans-acting factors. O-GlcNAcylation is a dynamic and reversible posttranslational modification of nuclear and cytoplasmic proteins that regulates various protein functions, including DNA-binding affinity and protein-protein interactions. However, the effects of O-GlcNAcylation on proteins involved in V(D)J recombination remain largely unknown. To elucidate this relationship, we downregulated O-GlcNAcylation in a mouse model by administering an O-GlcNAc inhibitor or restricting the consumption of a regular diet. Interestingly, the inhibition of O-GlcNAcylation in mi</pubmed_abstract><journal>Cellular &amp; molecular immunology</journal><pubmed_title>Dynamic O-GlcNAcylation governs long-range chromatin interactions in V(D)J recombination during early B-cell development.</pubmed_title><pmcid>PMC11686140</pmcid><funding_grant_id>KGM9942421</funding_grant_id><funding_grant_id>NTC2642311</funding_grant_id><funding_grant_id>2021R1I1A2057945</funding_grant_id><funding_grant_id>2021R1A2C1012477</funding_grant_id><funding_grant_id>2022M3E5F1016693</funding_grant_id><funding_grant_id>ZYM9382312</funding_grant_id><funding_grant_id>2020R1I1A3073845</funding_grant_id><pubmed_authors>Park AK</pubmed_authors><pubmed_authors>Jeon BC</pubmed_authors><pubmed_authors>Park Y</pubmed_authors><pubmed_authors>Kim TD</pubmed_authors><pubmed_authors>Kim YJ</pubmed_authors><pubmed_authors>Na KM</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Hwang H</pubmed_authors><pubmed_authors>Lim J</pubmed_authors><pubmed_authors>Song MR</pubmed_authors><pubmed_authors>An D</pubmed_authors><pubmed_authors>Park SK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamic O-GlcNAcylation governs long-range chromatin interactions in V(D)J recombination during early B-cell development.</name><description>V(D)J recombination secures the production of functional immunoglobulin (Ig) genes and antibody diversity during the early stages of B-cell development through long-distance interactions mediated by cis-regulatory elements and trans-acting factors. O-GlcNAcylation is a dynamic and reversible posttranslational modification of nuclear and cytoplasmic proteins that regulates various protein functions, including DNA-binding affinity and protein-protein interactions. However, the effects of O-GlcNAcylation on proteins involved in V(D)J recombination remain largely unknown. To elucidate this relationship, we downregulated O-GlcNAcylation in a mouse model by administering an O-GlcNAc inhibitor or restricting the consumption of a regular diet. Interestingly, the inhibition of O-GlcNAcylation in mi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-06T19:57:32.708Z</modification><creation>2026-06-04T03:12:32.755Z</creation></dates><accession>S-EPMC11686140</accession><cross_references><pubmed>39627609</pubmed><doi>10.1038/s41423-024-01236-9</doi></cross_references></HashMap>