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Inherited nuclear pore substructures template post-mitotic pore assembly.
Chou, Yi-Ying; Upadhyayula, Srigokul; Houser, Justin; He, Kangmin; Skillern, Wesley; Scanavachi, Gustavo; Dang, Song; Sanyal, Anwesha; Ohashi, Kazuka G; Di Caprio, Giuseppe; Kreutzberger, Alex J B; Vadakkan, Tegy John; Kirchhausen, Tom.
Afiliação
  • Chou YY; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Upadhyayula S; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115,
  • Houser J; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • He K; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115,
  • Skillern W; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Scanavachi G; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Dang S; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Sanyal A; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Ohashi KG; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Di Caprio G; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Kreutzberger AJB; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Vadakkan TJ; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA.
  • Kirchhausen T; Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA; Program in Cellular and Molecular Medicine, Boston Children's Hospital, 200 Longwood Avenue, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115,
Dev Cell ; 56(12): 1786-1803.e9, 2021 06 21.
Article em En | MEDLINE | ID: mdl-34129835
Nuclear envelope assembly during late mitosis includes rapid formation of several thousand complete nuclear pore complexes (NPCs). This efficient use of NPC components (nucleoporins or "NUPs") is essential for ensuring immediate nucleocytoplasmic communication in each daughter cell. We show that octameric subassemblies of outer and inner nuclear pore rings remain intact in the mitotic endoplasmic reticulum (ER) after NPC disassembly during prophase. These "inherited" subassemblies then incorporate into NPCs during post-mitotic pore formation. We further show that the stable subassemblies persist through multiple rounds of cell division and the accompanying rounds of NPC mitotic disassembly and post-mitotic assembly. De novo formation of NPCs from newly synthesized NUPs during interphase will then have a distinct initiation mechanism. We postulate that a yet-to-be-identified modification marks and "immortalizes" one or more components of the specific octameric outer and inner ring subcomplexes that then template post-mitotic NPC assembly during subsequent cell cycles.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Núcleo Celular / Poro Nuclear / Complexo de Proteínas Formadoras de Poros Nucleares / Mitose Limite: Humans Idioma: En Revista: Dev Cell Assunto da revista: EMBRIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Núcleo Celular / Poro Nuclear / Complexo de Proteínas Formadoras de Poros Nucleares / Mitose Limite: Humans Idioma: En Revista: Dev Cell Assunto da revista: EMBRIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos