|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
First published online January 10, 2008
doi: 10.1242/10.1242/jcs.005777
Commentary |
Salk Institute for Biological Studies, Molecular and Cell Biology Laboratory, 10010 N. Torrey Pines Road, La Jolla, CA 92037, USA
* Author for correspondence (e-mail: hetzer{at}salk.edu)
Accepted 7 November 2007
The nuclear envelope (NE), a double membrane enclosing the nucleus of eukaryotic cells, controls the flow of information between the nucleoplasm and the cytoplasm and provides a scaffold for the organization of chromatin and the cytoskeleton. In dividing metazoan cells, the NE breaks down at the onset of mitosis and then reforms around segregated chromosomes to generate the daughter nuclei. Recent data from intact cells and cell-free nuclear assembly systems suggest that the endoplasmic reticulum (ER) is the source of membrane for NE assembly. At the end of mitosis, ER membrane tubules are targeted to chromatin via tubule ends and reorganized into flat nuclear membrane sheets by specific DNA-binding membrane proteins. In contrast to previous models, which proposed vesicle fusion to be the principal mechanism of NE formation, these new studies suggest that the nuclear membrane forms by the chromatin-mediated reshaping of the ER.
Key words: Nuclear envelope, Endoplasmic reticulum, Membrane sheets, Tubules, DNA-binding membrane proteins, Open mitosis
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
F. Vollmar, C. Hacker, R.-P. Zahedi, A. Sickmann, A. Ewald, U. Scheer, and M.-C. Dabauvalle Assembly of nuclear pore complexes mediated by major vault protein J. Cell Sci., March 15, 2009; 122(6): 780 - 786. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Haraguchi, T. Kojidani, T. Koujin, T. Shimi, H. Osakada, C. Mori, A. Yamamoto, and Y. Hiraoka Live cell imaging and electron microscopy reveal dynamic processes of BAF-directed nuclear envelope assembly J. Cell Sci., August 1, 2008; 121(15): 2540 - 2554. [Abstract] [Full Text] [PDF] |
||||