Chromatin architecture may dictate the target site for DMC1, but not for RAD51, during homologous pairing-Reference-Cited by-同舟云学术

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Chromatin architecture may dictate the target site for DMC1, but not for RAD51, during homologous pairing

Published:2016-04 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Kobayashi Wataru,Takaku Motoki,Machida Shinichi,Tachiwana Hiroaki,Maehara Kazumitsu,Ohkawa Yasuyuki,Kurumizaka Hitoshi

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep24228.pdf

Reference62 articles.

1. Neale, M. J. & Keeney, S. Clarifying the mechanics of DNA strand exchange in meiotic recombination. Nature 442, 153–158 (2006).

2. Keeney, S. Spo11 and the formation of DNA double-strand breaks in meiosis. In Recombination and Meiosis (eds. Egel R., Lankenau D.-H. ). pp. 81–123. Springer-Verlag, Berlin Heidelberg (2007).

3. Bergerat, A. et al. An atypical topoisomerase II from Archaea with implications for meiotic recombination. Nature 386, 414–417 (1997).

4. Keeney, S., Giroux, C. N. & Kleckner, N. Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family. Cell 88, 375–384 (1997).

5. Neale, M. J., Pan, J. & Keeney, S. Endonucleolytic processing of covalent protein-linked DNA double-strand breaks. Nature 436, 1053–1057 (2005).

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3. Molecular structures and mechanisms of DNA break processing in mouse meiosis;Genes & Development;2020-04-30

4. The intrinsic ability of double-stranded DNA to carry out D-loop and R-loop formation;Computational and Structural Biotechnology Journal;2020

5. Cryo-EM Structures of Centromeric Tri-nucleosomes Containing a Central CENP-A Nucleosome;Structure;2020-01

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