A cDNA clone encoding a portion of Drosophila nuclear lamins Dm1 and Dm2 has been identified by screening a lambda-gt11 cDNA expression library using Drosophila lamin-specific monoclonal antibodies. Two different developmentally regulated mRNA species were identified by Northern blot analysis using the initial cDNA as a probe, and full-length cDNA clones, apparently corresponding to each message, have been isolated. In vitro transcription of both full-length cDNA clones in a pT7 transcription vector followed by in vitro translation in wheat germ lysate suggests that both clones encode lamin Dm0, the polypeptide precursor of lamins Dm1 and Dm2. Nucleotide sequence analyses confirm the impression that both cDNA clones code for the identical polypeptide, which is highly homologous with human lamins A and C as well as with mammalian intermediate filament proteins. The two clones differ in their 3'-untranslated regions. In situ hybridization of lamin cDNA clones to Drosophila polytene chromosomes shows only a single locus of hybridization at or near position 25F on the left arm of chromosome 2. Southern blot analyses of genomic DNA are consistent with the notion that a single or only a few highly similar genes encoding Drosophila nuclear lamin Dm0 exist in the genome.
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1 March 1988
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March 01 1988
Drosophila nuclear lamin precursor Dm0 is translated from either of two developmentally regulated mRNA species apparently encoded by a single gene.
Y Gruenbaum,
Y Gruenbaum
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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Y Landesman,
Y Landesman
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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B Drees,
B Drees
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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J W Bare,
J W Bare
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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H Saumweber,
H Saumweber
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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M R Paddy,
M R Paddy
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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J W Sedat,
J W Sedat
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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D E Smith,
D E Smith
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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B M Benton,
B M Benton
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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P A Fisher
P A Fisher
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
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Y Gruenbaum
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
Y Landesman
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
B Drees
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
J W Bare
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
H Saumweber
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
M R Paddy
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
J W Sedat
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
D E Smith
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
B M Benton
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
P A Fisher
Department of Biochemistry and Biophysics, University of California at San Francisco 94143.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1988) 106 (3): 585–596.
Citation
Y Gruenbaum, Y Landesman, B Drees, J W Bare, H Saumweber, M R Paddy, J W Sedat, D E Smith, B M Benton, P A Fisher; Drosophila nuclear lamin precursor Dm0 is translated from either of two developmentally regulated mRNA species apparently encoded by a single gene.. J Cell Biol 1 March 1988; 106 (3): 585–596. doi: https://doi.org/10.1083/jcb.106.3.585
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