spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bossie, C. A.
Right arrow Articles by Sanders, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bossie, C. A.
Right arrow Articles by Sanders, M. M.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Journal of Cell Science, Vol 104, Issue 4 1263-1272, Copyright © 1993 by Company of Biologists


JOURNAL ARTICLES

A cDNA from Drosophila melanogaster encodes a lamin C-like intermediate filament protein

CA Bossie and MM Sanders
Department of Pharmacology, UMDNJ - Robert Wood Johnson Medical School, Piscataway 08854.

A novel intermediate filament cDNA, pG-IF, has been isolated from a Drosophila melanogaster embryonic expression library screened with a polyclonal antiserum produced against a 46 kDa cytoskeletal protein isolated from Kc cells. This 46 kDa protein is known to be immunologically related to vertebrate intermediate filament proteins. The screen resulted in the isolation of four different cDNA groups. Of these, one has been identified as the previously characterized Drosophila nuclear lamin cDNA, Dm0, and a second, pG-IF, demonstrates homology to Dm0 by cross hybridization on Southern blots. DNA sequence analysis reveals that pG-IF encodes a newly identified intermediate filament protein in Drosophila. Its nucleotide sequence is highly homologous to nuclear lamins with lower homology to cytoplasmic intermediate filament proteins. pG-IF predicts a protein of 621 amino acids with a predicted molecular mass of 69,855 daltons. In vitro transcription and translation of pG-IF yielded a protein with a SDS-PAGE estimated molecular weight of approximately 70 kDa. It contains sequence principles characteristic of class V intermediate filament proteins. Its near neutral pI (6.83) and the lack of a terminal CaaX motif suggests that it may represent a lamin C subtype in Drosophila. In situ hybridization to polytene chromosomes detects one band of hybridization on the right arm of chromosome 2 at or near 51A. This in conjunction with Southern blot analysis of various genomic digests suggests one or more closely placed genes while Northern blot analysis detects two messages in Kc cells.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Cell Sci.Home page
A. Mattout, M. Goldberg, Y. Tzur, A. Margalit, and Y. Gruenbaum
Specific and conserved sequences in D. melanogaster and C. elegans lamins and histone H2A mediate the attachment of lamins to chromosomes
J. Cell Sci., January 1, 2007; 120(1): 77 - 85.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
R. D. Goldman, Y. Gruenbaum, R. D. Moir, D. K. Shumaker, and T. P. Spann
Nuclear lamins: building blocks of nuclear architecture
Genes & Dev., March 1, 2002; 16(5): 533 - 547.
[Full Text] [PDF]


Home page
Mol. Biol. CellHome page
J. Liu, T. R. Ben-Shahar, D. Riemer, M. Treinin, P. Spann, K. Weber, A. Fire, and Y. Gruenbaum
Essential Roles for Caenorhabditis elegans Lamin Gene in Nuclear Organization, Cell Cycle Progression, and Spatial Organization of Nuclear Pore Complexes
Mol. Biol. Cell, November 1, 2000; 11(11): 3937 - 3947.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Goldberg, A. Harel, M. Brandeis, T. Rechsteiner, T. J. Richmond, A. M. Weiss, and Y. Gruenbaum
The tail domain of lamin Dm0 binds histones H2A and H2B
PNAS, March 16, 1999; 96(6): 2852 - 2857.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. Goldberg, H. Lu, N. Stuurman, R. Ashery-Padan, A. M. Weiss, J. Yu, D. Bhattacharyya, P. A. Fisher, Y. Gruenbaum, and M. F. Wolfner
Interactions among Drosophila Nuclear Envelope Proteins Lamin, Otefin, and YA
Mol. Cell. Biol., July 1, 1998; 18(7): 4315 - 4323.
[Abstract] [Full Text]


Home page
J. Cell Sci.Home page
R Rzepecki, S. Bogachev, E Kokoza, N Stuurman, and P. Fisher
In vivo association of lamins with nucleic acids in Drosophila melanogaster
J. Cell Sci., January 1, 1998; 111(1): 121 - 129.
[Abstract] [PDF]


Home page
JCBHome page
B. Lenz-Bohme, J. Wismar, S. Fuchs, R. Reifegerste, E. Buchner, H. Betz, and B. Schmitt
Insertional Mutation of the Drosophila Nuclear Lamin Dm0 Gene Results in Defective Nuclear Envelopes, Clustering of Nuclear Pore Complexes, and Accumulation of Annulate Lamellae
J. Cell Biol., June 2, 1997; 137(5): 1001 - 1016.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
M Klapper, K Exner, A Kempf, C Gehrig, N Stuurman, P. Fisher, and G Krohne
Assembly of A- and B-type lamins studied in vivo with the baculovirus system
J. Cell Sci., January 10, 1997; 110(20): 2519 - 2532.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
D Riemer, N Stuurman, M Berrios, C Hunter, P. Fisher, and K Weber
Expression of Drosophila lamin C is developmentally regulated: analogies with vertebrate A-type lamins
J. Cell Sci., January 10, 1995; 108(10): 3189 - 3198.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
N Stuurman, N Maus, and P. Fisher
Interphase phosphorylation of the Drosophila nuclear lamin: site-mapping using a monoclonal antibody
J. Cell Sci., January 9, 1995; 108(9): 3137 - 3144.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
H Hennekes and E. Nigg
The role of isoprenylation in membrane attachment of nuclear lamins. A single point mutation prevents proteolytic cleavage of the lamin A precursor and confers membrane binding properties
J. Cell Sci., January 4, 1994; 107(4): 1019 - 1029.
[Abstract] [PDF]




© The Company of Biologists Ltd 1993