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Specific Roles of XRCC4 Paralogs PAXX and XLF during V(D)J Recombination
- Source :
- Cell Reports, Cell Reports, Elsevier Inc, 2016, ⟨10.1016/j.celrep.2016.08.069⟩, Cell Reports, Vol 16, Iss 11, Pp 2967-2979 (2016), Cell Reports, 2016, ⟨10.1016/j.celrep.2016.08.069⟩
- Publication Year :
- 2016
- Publisher :
- Cell Press, 2016.
-
Abstract
- Summary Paralog of XRCC4 and XLF (PAXX) is a member of the XRCC4 superfamily and plays a role in nonhomologous end-joining (NHEJ), a DNA repair pathway critical for lymphocyte antigen receptor gene assembly. Here, we find that the functions of PAXX and XLF in V(D)J recombination are masked by redundant joining activities. Thus, combined PAXX and XLF deficiency leads to an inability to join RAG-cleaved DNA ends. Additionally, we demonstrate that PAXX function in V(D)J recombination depends on its interaction with Ku. Importantly, we show that, unlike XLF, the role of PAXX during the repair of DNA breaks does not overlap with ATM and the RAG complex. Our findings illuminate the role of PAXX in V(D)J recombination and support a model in which PAXX and XLF function during NHEJ repair of DNA breaks, whereas XLF, the RAG complex, and the ATM-dependent DNA damage response promote end joining by stabilizing DNA ends.<br />Graphical Abstract Image 1<br />Highlights • PAXX-deficient pro-B cells support normal V(D)J recombination • PAXX and XLF are mutually redundant in repairing RAG-DNA breaks • PAXX function in V(D)J recombination depends on its interaction with Ku • Unlike XLF, PAXX is not redundant with ATM and the RAG complex in repairing DNA breaks<br />Developing lymphocytes rely on nonhomologous end joining (NHEJ) to repair programmed DNA double-strand breaks generated during antigen receptor gene assembly. Lescale et al. show that PAXX—a component of the NHEJ machinery—has a key role in V(D)J recombination that is masked by functional redundancy with its paralog XLF.
- Subjects :
- 0301 basic medicine
DNA Repair
DNA damage
DNA repair
Immunoglobulins
[SDV.CAN]Life Sciences [q-bio]/Cancer
Ataxia Telangiectasia Mutated Proteins
LIG4
Biology
[SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology
XLF
PAXX
Models, Biological
General Biochemistry, Genetics and Molecular Biology
Article
03 medical and health sciences
chemistry.chemical_compound
[SDV.CAN] Life Sciences [q-bio]/Cancer
Animals
Gene Rearrangement, B-Lymphocyte
Oncogene Proteins v-abl
lcsh:QH301-705.5
XRCC4
Ku Autoantigen
NHEJ
Genetics
Gene Editing
B-Lymphocytes
Sequence Homology, Amino Acid
V(D)J recombination
[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology
DNA repair protein XRCC4
V(D)J Recombination
Non-homologous end joining
DNA-Binding Proteins
030104 developmental biology
DNA Repair Enzymes
chemistry
lcsh:Biology (General)
[SDV.IMM.IA]Life Sciences [q-bio]/Immunology/Adaptive immunology
[SDV.IMM.IA] Life Sciences [q-bio]/Immunology/Adaptive immunology
CRISPR-Cas Systems
Recombination
DNA
Gene Deletion
DNA Damage
Subjects
Details
- Language :
- English
- ISSN :
- 22111247
- Database :
- OpenAIRE
- Journal :
- Cell Reports, Cell Reports, Elsevier Inc, 2016, ⟨10.1016/j.celrep.2016.08.069⟩, Cell Reports, Vol 16, Iss 11, Pp 2967-2979 (2016), Cell Reports, 2016, ⟨10.1016/j.celrep.2016.08.069⟩
- Accession number :
- edsair.doi.dedup.....f3b71045a3bd84fac2350e0b2ce23a1d
- Full Text :
- https://doi.org/10.1016/j.celrep.2016.08.069