|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 104, Issue 4 1263-1272, Copyright © 1993 by Company of Biologists
JOURNAL ARTICLES |
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.
This article has been cited by other articles:
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||