Specific Roles of XRCC4 Paralogs PAXX and XLF during V(D)J Recombination
Author(s) -
Chloé Lescale,
Hélène Lenden Hasse,
Andrew N. Blackford,
Gabriel Balmus,
Joy J. Bianchi,
Wei Yu,
Léa Bacoccina,
Angélique Jarade,
Christophe Clouin,
Rohan Sivapalan,
Bernardo ReinaSanMartin,
Stephen P. Jackson,
Ludovic Deriano
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.08.069
Subject(s) - v(d)j recombination , non homologous end joining , dna repair protein xrcc4 , dna repair , dna , biology , recombination , rag2 , genetics , dna pkcs , gene , microbiology and biotechnology , dna mismatch repair
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.
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