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Specific Roles of XRCC4 Paralogs PAXX and XLF during V(D)J Recombination

Authors :
Hélène Lenden Hasse
Chloé Lescale
Bernardo Reina-San-Martin
Stephen P. Jackson
Léa Bacoccina
Gabriel Balmus
Joy J. Bianchi
Ludovic Deriano
Rohan Sivapalan
Christophe Clouin
Angélique Jarade
Andrew N. Blackford
Wei Yu
Institut Pasteur [Paris]
University of Oxford [Oxford]
The Wellcome Trust Sanger Institute [Cambridge]
University of Cambridge [UK] (CAM)
Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)
The Jackson Laboratory is funded by Cancer Research UK program grant C6/A18796 and the European Research Council. Core infrastructure funding is provided by CRUK (C6946/A14492) and the Wellcome Trust (WT092096). S.P.J. receives his salary from the University of Cambridge, which is supplemented by CRUK. G.B. and A.N.B. are supported by CRUK (C6/A18796). The L.D. laboratory is funded by the Institut Pasteur as well as the European Research Council under the ERC starting grant agreement no. 310917.
European Project: 310917,EC:FP7:ERC,ERC-2012-StG_20111109,LYMPHOONCOGENOMICS(2013)
DERIANO, Ludovic
Deciphering the Oncogenic Lesions and Pathways of B and T Cell Cancers - LYMPHOONCOGENOMICS - - EC:FP7:ERC2013-02-01 - 2018-01-31 - 310917 - VALID
Institut Pasteur [Paris] (IP)
University of Oxford
Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Balmus, Gabriel [0000-0003-2872-4468]
Jackson, Stephen [0000-0001-9317-7937]
Apollo - University of Cambridge Repository
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.

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