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dc.contributor.authorCastaneda Zegarra, Sergio Miguel
dc.contributor.authorZhang, Qindong
dc.contributor.authorAlirezaylavasani, Amin
dc.contributor.authorFernandez-Berrocal, Marion Silvana
dc.contributor.authorYao, Rouan
dc.contributor.authorOksenych, Valentyn
dc.date.accessioned2021-03-01T21:46:26Z
dc.date.available2021-03-01T21:46:26Z
dc.date.issued2020-12-07
dc.description.abstractNon-homologous end-joining (NHEJ) is a DNA repair pathway required to detect, process, and ligate DNA double-stranded breaks (DSBs) throughout the cell cycle. The NHEJ pathway is necessary for V(D)J recombination in developing B and T lymphocytes. During NHEJ, Ku70 and Ku80 form a heterodimer that recognizes DSBs and promotes recruitment and function of downstream factors PAXX, MRI, DNA-PKcs, Artemis, XLF, XRCC4, and LIG4. Mutations in several known NHEJ genes result in severe combined immunodeficiency (SCID). Inactivation of Mri, Paxx or Xlf in mice results in normal or mild phenotype, while combined inactivation of Xlf/Mri, Xlf/Paxx, or Xlf/Dna-pkcs leads to late embryonic lethality. Here, we describe three new mouse models. We demonstrate that deletion of Trp53 rescues embryonic lethality in mice with combined deficiencies of Xlf and Mri. Furthermore, Xlf-/-Mri-/-Trp53+/- and Xlf-/-Paxx-/-Trp53+/- mice possess reduced body weight, severely reduced mature lymphocyte counts, and accumulation of progenitor B cells. We also report that combined inactivation of Mri/Paxx results in live-born mice with modest phenotype, and combined inactivation of Mri/Dna-pkcs results in embryonic lethality. Therefore, we conclude that XLF is functionally redundant with MRI and PAXX during lymphocyte development in vivo. Moreover, Mri genetically interacts with Dna-pkcs and Paxx.en_US
dc.identifier.citationCastaneda Zegarra Castaneda-Zegarra S, Zhang Q, Alirezaylavasani A, Fernandez-Berrocal MS, Yao R, Oksenych V. Leaky severe combined immunodeficiency in mice lacking non-homologous end joining factors XLF and MRI. Aging. 2020;12(23):23578-23597en_US
dc.identifier.cristinIDFRIDAID 1860501
dc.identifier.doi10.18632/aging.202346
dc.identifier.issn1945-4589
dc.identifier.urihttps://hdl.handle.net/10037/20628
dc.language.isoengen_US
dc.publisherImpact Journals, LLCen_US
dc.relation.journalAging
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/FRIMEDBIO/249774/Norway/Mechanisms underlying the function of XLF in DNA double-strand break repair//en_US
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/POS-ERC/270491/Norway/Role of novel DNA double strand break repair factors in immune system development//en_US
dc.relation.urihttps://www.aging-us.com/article/202346/text
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2020 The Author(s)en_US
dc.subjectVDP::Mathematics and natural science: 400::Basic biosciences: 470::Cell biology: 471en_US
dc.subjectVDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470::Cellebiologi: 471en_US
dc.titleLeaky severe combined immunodeficiency in mice lacking non-homologous end joining factors XLF and MRIen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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