|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
First published online 16 November 2004
doi: 10.1242/jcs.01532
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Article |
Division of Electron Microscopy, Biocenter of the University of Würzburg, Am Hubland, 97074 Würzburg, Germany
* Author for correspondence (e-mail: krohne{at}biozentrum.uni-wuerzburg.de)
Accepted 13 September 2004
We analyzed the influence of lamins on nuclear envelope growth in cultured Xenopus A6 cells by the overexpression of human lamin A, Xenopus and zebrafish lamins B2 and Drosophila lamins Dm0 and C as GFP fusion proteins. Lamins containing a CxxM motif in their primary sequence (lamins A, B2, Dm0) induced the formation of lobulated nuclei with multi-membrane-layered, highly folded nuclear membranes and intranuclear membrane assemblies, as observed by electron microscopy. Such morphological alterations were not observed with Drosophila lamin C, a lamin without this motif or with a lamin B2 mutant (B2-SxxM) where the cysteine of the CxxM motif is replaced by a serine. Drosophila lamin C mutants containing a CxxM motif behaved like B-type lamins thus confirming that this tetrapeptide is directly involved in the morphological changes we observed. Nuclear membrane proliferation could also be induced by lamin B2 in COS-7 cells and in zebrafish embryos but not by human lamin A in COS-7 cells. We speculate that the human lamin A is incompletely processed in Xenopus A6 cells and therefore behaves in this cell line like a B-type lamin. Our results indicate that the CxxM motif of B-type lamins has a dual function: it mediates lamin targeting to the inner nuclear membrane thereby promoting nuclear membrane growth.
Key words: Lamin, CxxM motif, Nuclear envelope, Intranuclear membranes, Nuclear membrane proliferation
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
S.-T. Lin and Y.-H. Fu miR-23 regulation of lamin B1 is crucial for oligodendrocyte development and myelination Dis. Model. Mech., March 1, 2009; 2(3-4): 178 - 188. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Guffanti, N. Kittur, Z. N. Brodt, A. J. Polotsky, S. M. Kuokkanen, D. S. Heller, S. L. Young, N. Santoro, and U. T. Meier Nuclear pore complex proteins mark the implantation window in human endometrium J. Cell Sci., June 15, 2008; 121(12): 2037 - 2045. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Luke, H. Zaim, I. Karakesisoglou, V. M. Jaeger, L. Sellin, W. Lu, M. Schneider, S. Neumann, A. Beijer, M. Munck, et al. Nesprin-2 Giant (NUANCE) maintains nuclear envelope architecture and composition in skin J. Cell Sci., June 1, 2008; 121(11): 1887 - 1898. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Goldberg, I. Huttenlauch, C. J. Hutchison, and R. Stick Filaments made from A- and B-type lamins differ in structure and organization J. Cell Sci., January 15, 2008; 121(2): 215 - 225. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Gehrig, R. B. Cornell, and N. D. Ridgway Expansion of the Nucleoplasmic Reticulum Requires the Coordinated Activity of Lamins and CTP:Phosphocholine Cytidylyltransferase {alpha} Mol. Biol. Cell, January 1, 2008; 19(1): 237 - 247. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. G. Klupp, H. Granzow, W. Fuchs, G. M. Keil, S. Finke, and T. C. Mettenleiter Vesicle formation from the nuclear membrane is induced by coexpression of two conserved herpesvirus proteins PNAS, April 24, 2007; 104(17): 7241 - 7246. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Snyers, S. Vlcek, T. Dechat, D. Skegro, B. Korbei, A. Gajewski, O. Mayans, C. Schofer, and R. Foisner Lamina-associated Polypeptide 2-{alpha} Forms Homo-trimers via Its C Terminus, and Oligomerization Is Unaffected by a Disease-causing Mutation J. Biol. Chem., March 2, 2007; 282(9): 6308 - 6315. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. L.R.M. Verstraeten, J. L.V. Broers, M. A.M. van Steensel, S. Zinn-Justin, F. C.S. Ramaekers, P. M. Steijlen, M. Kamps, H. J.H. Kuijpers, D. Merckx, H. J.M. Smeets, et al. Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation Hum. Mol. Genet., August 15, 2006; 15(16): 2509 - 2522. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. V. Broers, F. C. S. Ramaekers, G. Bonne, R. B. Yaou, and C. J. Hutchison Nuclear lamins: laminopathies and their role in premature ageing. Physiol Rev, July 1, 2006; 86(3): 967 - 1008. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Delbarre, M. Tramier, M. Coppey-Moisan, C. Gaillard, J.-C. Courvalin, and B. Buendia The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers Hum. Mol. Genet., April 1, 2006; 15(7): 1113 - 1122. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. McClintock, L. B. Gordon, and K. Djabali Hutchinson-Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody PNAS, February 14, 2006; 103(7): 2154 - 2159. [Abstract] [Full Text] [PDF] |
||||