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Real-time tracking reveals catalytic roles for the two DNA binding sites of Rad51.
Ito, Kentaro; Murayama, Yasuto; Kurokawa, Yumiko; Kanamaru, Shuji; Kokabu, Yuichi; Maki, Takahisa; Mikawa, Tsutomu; Argunhan, Bilge; Tsubouchi, Hideo; Ikeguchi, Mitsunori; Takahashi, Masayuki; Iwasaki, Hiroshi.
Affiliation
  • Ito K; Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
  • Murayama Y; Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
  • Kurokawa Y; Center for Frontier Research, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, 411-8540, Japan.
  • Kanamaru S; Department of Genetics, SOKENDAI (The Graduate University for Advanced Studies), 1111 Yata, Mishima, Shizuoka, 411-8540, Japan.
  • Kokabu Y; Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
  • Maki T; Center for Frontier Research, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, 411-8540, Japan.
  • Mikawa T; Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
  • Argunhan B; School and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
  • Tsubouchi H; Graduate School of Medical Life Science, Yokohama City University, 1-7-29 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.
  • Ikeguchi M; Department of Bioscience, Mitsui Knowledge Industry, 2-5-1 Atago, Minato-ku, Tokyo, 105-6215, Japan.
  • Takahashi M; Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
  • Iwasaki H; RIKEN Center for Biosystems Dynamics Research, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.
Nat Commun ; 11(1): 2950, 2020 06 11.
Article in En | MEDLINE | ID: mdl-32528002
ABSTRACT
During homologous recombination, Rad51 forms a nucleoprotein filament on single-stranded DNA to promote DNA strand exchange. This filament binds to double-stranded DNA (dsDNA), searches for homology, and promotes transfer of the complementary strand, producing a new heteroduplex. Strand exchange proceeds via two distinct three-strand intermediates, C1 and C2. C1 contains the intact donor dsDNA whereas C2 contains newly formed heteroduplex DNA. Here, we show that the conserved DNA binding motifs, loop 1 (L1) and loop 2 (L2) in site I of Rad51, play distinct roles in this process. L1 is involved in formation of the C1 complex whereas L2 mediates the C1-C2 transition, producing the heteroduplex. Another DNA binding motif, site II, serves as the DNA entry position for initial Rad51 filament formation, as well as for donor dsDNA incorporation. Our study provides a comprehensive molecular model for the catalytic process of strand exchange mediated by eukaryotic RecA-family recombinases.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Rad51 Recombinase Limits: Humans Language: En Journal: Nat Commun Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Rad51 Recombinase Limits: Humans Language: En Journal: Nat Commun Year: 2020 Document type: Article