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PMID: 21601571 Published · ppublish English

Valine 1532 of human BRC repeat 4 plays an important role in the interaction between BRCA2 and RAD51.

FEBS letters ·Vol. 585 ·No. 12 ·2011-09-05

Ochiai Kazuhiko, Yoshikawa Yasunaga, Yoshimatsu Kumiko, Oonuma Toshina, Tomioka Yukiko, Takeda Eichi, Arikawa Jiro, Mominoki Katsumi, Omi Toshinori, Hashizume Kazuyoshi, Morimatsu Masami

Abstract

The breast cancer susceptibility protein BRCA2 is essential for recombinational DNA repair. BRCA2 specifically binds to RAD51 via eight BRC repeat motifs and delivers RAD51 to double-stranded DNA breaks. In this study, a mammalian two-hybrid assay and competitive ELISA showed that the interaction between BRC repeat 4 (BRC4) and RAD51 was strengthened by the substitution of a single BRC4 amino acid from valine to isoleucine (V1532I). However, the cancer-associated V1532F mutant exhibited very weak interaction with RAD51. This study used a comparative analysis of BRC4 between animal species to identify V1532 as an important residue that interacts with RAD51.

Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
Published
2011-09-05
Indexed
2011-06-09
Updated
2013-11-21
Language
English
Country/Region
England
NLM ID
0155157
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