Formation of the postmitotic nuclear envelope from extended ER cisternae precedes nuclear pore assembly

Author:

Lu Lei123,Ladinsky Mark S.44,Kirchhausen Tomas12

Affiliation:

1. Department of Cell Biology, Harvard Medical School, Boston, MA 02115

2. Immune Disease Institute and Program in Cellular and Molecular Medicine, Children’s Hospital Boston, Boston, MA 02115

3. School of Biological Sciences, Nanyang Technological University, Singapore 639798

4. Division of Biology and Howard Hughes Medical Institute, California Institute of Technology, Pasadena, CA 91125

Abstract

During mitosis, the nuclear envelope merges with the endoplasmic reticulum (ER), and nuclear pore complexes are disassembled. In a current model for reassembly after mitosis, the nuclear envelope forms by a reshaping of ER tubules. For the assembly of pores, two major models have been proposed. In the insertion model, nuclear pore complexes are embedded in the nuclear envelope after their formation. In the prepore model, nucleoporins assemble on the chromatin as an intermediate nuclear pore complex before nuclear envelope formation. Using live-cell imaging and electron microscope tomography, we find that the mitotic assembly of the nuclear envelope primarily originates from ER cisternae. Moreover, the nuclear pore complexes assemble only on the already formed nuclear envelope. Indeed, all the chromatin-associated Nup107–160 complexes are in single units instead of assembled prepores. We therefore propose that the postmitotic nuclear envelope assembles directly from ER cisternae followed by membrane-dependent insertion of nuclear pore complexes.

Publisher

Rockefeller University Press

Subject

Cell Biology

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