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Transfected plasmid DNA is incorporated into the nucleus via nuclear envelope reformation at telophase.
Haraguchi, Tokuko; Koujin, Takako; Shindo, Tomoko; Bilir, Sükriye; Osakada, Hiroko; Nishimura, Kohei; Hirano, Yasuhiro; Asakawa, Haruhiko; Mori, Chie; Kobayashi, Shouhei; Okada, Yasushi; Chikashige, Yuji; Fukagawa, Tatsuo; Shibata, Shinsuke; Hiraoka, Yasushi.
  • Haraguchi T; Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan. haraguchi@fbs.osaka-u.ac.jp.
  • Koujin T; Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe, 651-2492, Japan. haraguchi@fbs.osaka-u.ac.jp.
  • Shindo T; Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.
  • Bilir S; Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe, 651-2492, Japan.
  • Osakada H; Keio University, School of Medicine, Shinjuku-ku, Tokyo, 160-8582, Japan.
  • Nishimura K; Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.
  • Hirano Y; Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe, 651-2492, Japan.
  • Asakawa H; Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.
  • Mori C; Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.
  • Kobayashi S; Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.
  • Okada Y; Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe, 651-2492, Japan.
  • Chikashige Y; Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe, 651-2492, Japan.
  • Fukagawa T; RIKEN Center for Biosystems Dynamics Research (BDR), Suita, Osaka, 565-0874, Japan.
  • Shibata S; Department of Cell Biology, Department of Physics, Universal Biology Institute (UBI) and International Research Center for Neurointelligence (IRCN), the University of Tokyo, Tokyo, 113-0033, Japan.
  • Hiraoka Y; Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, 588-2 Iwaoka, Iwaoka-cho, Nishi-ku, Kobe, 651-2492, Japan.
Commun Biol ; 5(1): 78, 2022 01 20.
Article en En | MEDLINE | ID: mdl-35058555
ABSTRACT
DNA transfection is an important technology in life sciences, wherein nuclear entry of DNA is necessary to express exogenous DNA. Non-viral vectors and their transfection reagents are useful as safe transfection tools. However, they have no effect on the transfection of non-proliferating cells, the reason for which is not well understood. This study elucidates the mechanism through which transfected DNA enters the nucleus for gene expression. To monitor the behavior of transfected DNA, we introduce plasmid bearing lacO repeats and RFP-coding sequences into cells expressing GFP-LacI and observe plasmid behavior and RFP expression in living cells. RFP expression appears only after mitosis. Electron microscopy reveals that plasmids are wrapped with nuclear envelope (NE)‒like membranes or associated with chromosomes at telophase. The depletion of BAF, which is involved in NE reformation, delays plasmid RFP expression. These results suggest that transfected DNA is incorporated into the nucleus during NE reformation at telophase.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Plásmidos / ADN / Proteínas Nucleares / Núcleo Celular / Regulación de la Expresión Génica / Proteínas de la Membrana Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Plásmidos / ADN / Proteínas Nucleares / Núcleo Celular / Regulación de la Expresión Génica / Proteínas de la Membrana Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article