Author:
Kurumizaka Hitoshi,Ikawa Shukuko,Nakada Maki,Eda Keiko,Kagawa Wataru,Takata Minoru,Takeda Shunichi,Yokoyama Shigeyuki,Shibata Takehiko
Abstract
The human Xrcc3 protein is involved in the repair of damaged DNA
through homologous recombination, in which homologous pairing is a key
step. The Rad51 protein is believed to be the only protein factor that
promotes homologous pairing in recombinational DNA repair in mitotic
cells. In the brain, however, Rad51 expression is
extremely low, whereas XRCC3, a human homologue of
Saccharomyces cerevisiae RAD57 that activates the
Rad51-dependent homologous pairing with the yeast Rad55 protein, is
expressed. In this study, a two-hybrid analysis conducted with the use
of a human brain cDNA library revealed that the major Xrcc3-interacting
protein is a Rad51 paralog, Rad51C/Rad51L2. The purified
Xrcc3⋅Rad51C complex, which shows apparent 1:1 stoichiometry, was
found to catalyze the homologous pairing. Although the activity is
reduced, the Rad51C protein alone also catalyzed homologous pairing,
suggesting that Rad51C is a catalytic subunit for homologous pairing.
The DNA-binding activity of Xrcc3⋅Rad51C was drastically decreased
in the absence of Xrcc3, indicating that Xrcc3 is important for the DNA
binding of Xrcc3⋅Rad51C. Electron microscopic observations
revealed that Xrcc3⋅Rad51C and Rad51C formed similar filamentous
structures with circular single-stranded DNA.
Publisher
Proceedings of the National Academy of Sciences
Cited by
114 articles.
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