Location of Repository

Ku70 is required for DNA repair but not for T cell antigen receptor gene recombination

By Honghai Ouyang, Andre Nussenzweig, Akihiro Kurimasa, Vera Da Costa Soares, Xiaoling Li, Carlos Cordon-cardo, Wen-hui Li, Nge Cheong, Michel Nussenzweig, George Iliakis, David J. Chen and Gloria C. Li


Ku is a complex of two proteins, Ku70 and Ku80, and functions as a heterodimer to bind DNA double-strand breaks (DSB) and activate DNA-dependent protein kinase. The role of the Ku70 subunit in DNA DSB repair, hypersensitivity to ionizing radiation, and V(D)J recombination was examined in mice that lack Ku70 (Ku70 �/ �). Like Ku80 �/ � mice, Ku70 �/� mice showed a profound deficiency in DNA DSB repair and were proportional dwarfs. Surprisingly, in contrast to Ku80 �/ � mice in which both T and B lymphocyte development were arrested at an early stage, lack of Ku70 was compatible with T cell receptor gene recombination and the development of mature CD4 � CD8 � and CD4 � CD8 � T cells. Our data shows, for the first time, that Ku70 plays an essential role in DNA DSB repair, but is not required for TCR V(D)J recombination. These results suggest that distinct but overlapping repair pathways may mediate DNA DSB repair and V(D)J recombination. Two distinct processes involving DNA double-strand breaks (DSB) 1 have been identified in mammalian cells: the repair of DNA damage induced by ionizing radiation and V(D)J recombination during T and B cell development

Year: 1997
OAI identifier: oai:CiteSeerX.psu:
Provided by: CiteSeerX
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • http://citeseerx.ist.psu.edu/v... (external link)
  • http://jem.rupress.org/content... (external link)
  • Suggested articles

    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.