<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pfeifer M</submitter><funding>National Institute for Health Research (NIHR)</funding><funding>Marie Curie</funding><pagination>3423-3433</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6545462</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>202(12)</volume><pubmed_abstract>Induction of programmed DNA damage and its recognition and repair are fundamental for B cell development. The ssDNA-binding protein SSB1 has been described in human cells as essential for the recognition and repair of DNA damage. To study its relevance for B cells, we recently developed &lt;i>Ssb1&lt;/i> &lt;sup>-/-&lt;/sup> and conditional &lt;i>Ssb1&lt;/i> &lt;sup>-/-&lt;/sup> mice. Although SSB1 loss did not affect B cell development, &lt;i>Ssb1&lt;/i> &lt;sup>-/-&lt;/sup> cells exhibited compensatory expression of its homolog SSB2. We have now generated &lt;i>Ssb2&lt;/i> &lt;sup>-/-&lt;/sup> mice and show in this study that SSB2 is also dispensable for B cell development and DNA damage response activation. In contrast to the single loss of &lt;i>Ssb1&lt;/i> or &lt;i>Ssb2&lt;/i>, however, combined SSB1/2 deficiency caused a defect in early B cel</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>SSB1/SSB2 Proteins Safeguard B Cell Development by Protecting the Genomes of B Cell Precursors.</pubmed_title><pmcid>PMC6545462</pmcid><funding_grant_id>NIHR-RP-011-053</funding_grant_id><funding_grant_id>P49318</funding_grant_id><pubmed_authors>Robinson ME</pubmed_authors><pubmed_authors>Boulianne B</pubmed_authors><pubmed_authors>Lippert TP</pubmed_authors><pubmed_authors>Ho HN</pubmed_authors><pubmed_authors>Feldhahn N</pubmed_authors><pubmed_authors>Stebbing J</pubmed_authors><pubmed_authors>Pfeifer M</pubmed_authors><pubmed_authors>Brem R</pubmed_authors></additional><is_claimable>false</is_claimable><name>SSB1/SSB2 Proteins Safeguard B Cell Development by Protecting the Genomes of B Cell Precursors.</name><description>Induction of programmed DNA damage and its recognition and repair are fundamental for B cell development. The ssDNA-binding protein SSB1 has been described in human cells as essential for the recognition and repair of DNA damage. To study its relevance for B cells, we recently developed &lt;i>Ssb1&lt;/i> &lt;sup>-/-&lt;/sup> and conditional &lt;i>Ssb1&lt;/i> &lt;sup>-/-&lt;/sup> mice. Although SSB1 loss did not affect B cell development, &lt;i>Ssb1&lt;/i> &lt;sup>-/-&lt;/sup> cells exhibited compensatory expression of its homolog SSB2. We have now generated &lt;i>Ssb2&lt;/i> &lt;sup>-/-&lt;/sup> mice and show in this study that SSB2 is also dispensable for B cell development and DNA damage response activation. In contrast to the single loss of &lt;i>Ssb1&lt;/i> or &lt;i>Ssb2&lt;/i>, however, combined SSB1/2 deficiency caused a defect in early B cel</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2025-04-18T14:12:10.53Z</modification><creation>2019-07-24T07:08:11Z</creation></dates><accession>S-EPMC6545462</accession><cross_references><pubmed>31085591</pubmed><doi>10.4049/jimmunol.1801618</doi></cross_references></HashMap>