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Molecular architecture of G-quadruplex structures generated on duplex Rif1-binding sequences.
Masai, Hisao; Kakusho, Naoko; Fukatsu, Rino; Ma, Yue; Iida, Keisuke; Kanoh, Yutaka; Nagasawa, Kazuo.
Afiliación
  • Masai H; From the Department of Genome Medicine, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan, masai-hs@igakuken.or.jp.
  • Kakusho N; From the Department of Genome Medicine, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan.
  • Fukatsu R; From the Department of Genome Medicine, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan.
  • Ma Y; the Department of Biotechnology and Life Science, Faculty of Technology, Tokyo University of Agriculture and Technology, Tokyo 184-8588, Japan, and.
  • Iida K; the Molecular Chirality Research Center, Synthetic Organic Chemistry, Department of Chemistry, Graduate School of Science, Chiba University, Chiba 263-8522, Japan.
  • Kanoh Y; From the Department of Genome Medicine, Tokyo Metropolitan Institute of Medical Science, Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan.
  • Nagasawa K; the Department of Biotechnology and Life Science, Faculty of Technology, Tokyo University of Agriculture and Technology, Tokyo 184-8588, Japan, and.
J Biol Chem ; 293(44): 17033-17049, 2018 11 02.
Article en En | MEDLINE | ID: mdl-30217821
ABSTRACT
G-quadruplexes (G4s) are four-stranded DNA structures comprising stacks of four guanines, are prevalent in genomes, and have diverse biological functions in various chromosomal structures. A conserved protein, Rap1-interacting factor 1 (Rif1) from fission yeast (Schizosaccharomyces pombe), binds to Rif1-binding sequence (Rif1BS) and regulates DNA replication timing. Rif1BS is characterized by the presence of multiple G-tracts, often on both strands, and their unusual spacing. Although previous studies have suggested generation of G4-like structures on duplex Rif1BS, its precise molecular architecture remains unknown. Using gel-shift DNA binding assays and DNA footprinting with various nuclease probes, we show here that both of the Rif1BS strands adopt specific higher-order structures upon heat denaturation. We observed that the structure generated on the G-strand is consistent with a G4 having unusually long loop segments and that the structure on the complementary C-strand does not have an intercalated motif (i-motif). Instead, we found that the formation of the C-strand structure depends on the G4 formation on the G-strand. Thus, the higher-order structure generated at Rif1BS involved both DNA strands, and in some cases, G4s may form on both of these strands. The presence of multiple G-tracts permitted the formation of alternative structures when some G-tracts were mutated or disrupted by deazaguanine replacement, indicating the robust nature of DNA higher-order structures generated at Rif1BS. Our results provide general insights into DNA structures generated at G4-forming sequences on duplex DNA.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Schizosaccharomyces / ADN de Hongos / Proteínas de Schizosaccharomyces pombe / Proteínas de Unión a Telómeros Idioma: En Revista: J Biol Chem Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Schizosaccharomyces / ADN de Hongos / Proteínas de Schizosaccharomyces pombe / Proteínas de Unión a Telómeros Idioma: En Revista: J Biol Chem Año: 2018 Tipo del documento: Article