Cernunnos interacts with the XRCC4•DNA-ligase IV complex and is homologous to the yeast nonhomologous end-joining factor Nej1

被引:92
作者
Callebaut, Isabelle
Malivert, Laurent
Fischer, Alain
Mornon, Jean-Paul
Revy, Patrick
de Villartay, Jean-Pierre
机构
[1] Univ Paris 06, IMPMC, Dept Biol Struct, CNRS UMR 7590, F-75252 Paris 05, France
[2] Univ Paris 07, IMPMC, Dept Biol Struct, CNRS UMR 7590, F-75252 Paris 05, France
[3] Hop Necker Enfants Malad, INSERM, U768, Unite Dev Normal & Pathol Syst Immunitaire, F-75015 Paris, France
[4] Univ Paris 05, Fac Med Rene Descartes, F-75005 Paris, France
[5] Hop Necker Enfants Malad, AP HP, Unite Immunol & Hematol, F-75015 Paris, France
关键词
D O I
10.1074/jbc.C500473200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA double strand breaks are considered as the most harmful DNA lesions and are repaired by either homologous recombination or nonhomologous end joining (NHEJ). A new NHEJ factor, Cernunnos, has been identified, the defect of which leads to a severe immunodeficiency condition associated with microcephaly and other developmental defects in humans. This presentation is reminiscent to that of DNA-ligase IV deficiency and suggests a possible interplay between Cernunnos and the XRCC4 center dot DNA-ligase IV complex. We show here that Cernunnos physically interacts with the XRCC4 center dot DNA-ligase IV complex. Moreover, a combination of sensitive methods of sequence analysis revealed that Cernunnos can be associated with the XRCC4 family of proteins and that it corresponds to the genuine homolog of the yeast Nej1 protein. Altogether these results shed new lights on the last step, the DNA religation, of the NHEJ pathway.
引用
收藏
页码:13857 / 13860
页数:4
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