Abstract

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 x DNA-ligase IV complex. We show here that Cernunnos physically interacts with the XRCC4 x 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.

Highlights

  • Ku80 heterodimer, the DNA-PKcs kinase, the Artemis endonuclease, and the XRCC41⁄7DNA-ligase IV complex responsible for the final ligation step [3]

  • Additional nonhomologous end joining (NHEJ) factors have been recognized in yeast, such as Nej1, which interacts with the yeast XRCC4 homolog Lif1p (4 – 6)

  • Cernunnos Interacts with the XRCC41⁄7DNA-Ligase IV Complex—We searched for a possible interaction of Cernunnos with the XRCC41⁄7DNA-Ligase IV complex by transfecting 293T cells with a V5 epitope-tagged form of Cernunnos followed by immunoprecipitation experiments

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Summary

Introduction

Ku80 heterodimer, the DNA-PKcs kinase, the Artemis endonuclease, and the XRCC41⁄7DNA-ligase IV complex responsible for the final ligation step [3]. The immunoprecipitation of either endogenous DNA-ligase IV (lane 8) or XRCC4 (lane 10) co-precipitated the transfected Cernunnos protein (revealed by anti-V5 antibody, bottom panel) in both cases.

Results
Conclusion
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