<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>30(13)</volume><submitter>Brenner S</submitter><pubmed_abstract>The quality and quantity of BCR signals impact on cell fate decisions of B lymphocytes. Here, we describe novel gene-targeted mice, which in the context of normal VDJ recombination show hypomorphic expression of immunoglobulin μ heavy chain (μHC) mRNA levels and hence lower pre-BCR and BCR levels. Hypomorphic expression of μHC leads to augmented selection processes at all stages of B-cell development, noticeably at the expansion of pre-B cells, the positive selection of immature B lymphocytes in the bone marrow and the selection of the follicular (FO), marginal zone (MZ) and B1 B-lymphocyte compartment in peripheral lymphoid organs. Immature as well as mature FO and MZ B lymphocytes in the peripheral lymphoid organs express lower levels of the receptor for B-cell activating factor (BAFF). </pubmed_abstract><journal>The EMBO journal</journal><pagination>2705-18</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3155302</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A hypomorphic IgH-chain allele affects development of B-cell subsets and favours receptor editing.</pubmed_title><pmcid>PMC3155302</pmcid><pubmed_authors>Steinbart T</pubmed_authors><pubmed_authors>Welzel H</pubmed_authors><pubmed_authors>Yu P</pubmed_authors><pubmed_authors>Brenner S</pubmed_authors><pubmed_authors>Drewel D</pubmed_authors><pubmed_authors>Nitschke L</pubmed_authors><pubmed_authors>Weisel F</pubmed_authors><pubmed_authors>Schweizer A</pubmed_authors><pubmed_authors>Hartel E</pubmed_authors><pubmed_authors>Potzsch S</pubmed_authors><pubmed_authors>Brandl A</pubmed_authors><pubmed_authors>Mudde GC</pubmed_authors><pubmed_authors>Winkler TH</pubmed_authors></additional><is_claimable>false</is_claimable><name>A hypomorphic IgH-chain allele affects development of B-cell subsets and favours receptor editing.</name><description>The quality and quantity of BCR signals impact on cell fate decisions of B lymphocytes. Here, we describe novel gene-targeted mice, which in the context of normal VDJ recombination show hypomorphic expression of immunoglobulin μ heavy chain (μHC) mRNA levels and hence lower pre-BCR and BCR levels. Hypomorphic expression of μHC leads to augmented selection processes at all stages of B-cell development, noticeably at the expansion of pre-B cells, the positive selection of immature B lymphocytes in the bone marrow and the selection of the follicular (FO), marginal zone (MZ) and B1 B-lymphocyte compartment in peripheral lymphoid organs. Immature as well as mature FO and MZ B lymphocytes in the peripheral lymphoid organs express lower levels of the receptor for B-cell activating factor (BAFF). </description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 May</publication><modification>2025-05-29T20:29:03.376Z</modification><creation>2019-03-27T03:07:57Z</creation></dates><accession>S-EPMC3155302</accession><cross_references><pubmed>21623346</pubmed><doi>10.1038/emboj.2011.168</doi></cross_references></HashMap>