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Monoclonal antibodies to plant nuclear matrix reveal intermediate filament- related components within the nucleus
84
Citations
37
References
1991
Year
Immunocytochemical TechniqueIntermediate Filament AntibodyGeneticsPlant Molecular BiologyProteomicsPlant CytologyMonoclonal AntibodyNuclear OrganizationGene ExpressionPlant ProteomicsCell BiologyBiologyChromatinNatural SciencesSeed StorageCellular BiochemistryMonoclonal AntibodiesMedicinePlant Physiology
ABSTRACT We have prepared a nuclear matrix fraction from purified nuclei of carrot (Daucus carota L.) suspension culture cells, and used this fraction to produce a library of monoclonal antibodies. We report the preliminary characterisation of two antibodies – JIM 62 and JIM 63. The antibodies recognise a polypeptide doublet band at 92×103Mr, which has been partially purified by differential urea extraction. Other intermediate filament antibodies – ME 101, which recognises an epitope conserved among many intermediate filament proteins, and AFB, a monoclonal antibody to plant intermediate filament proteins, and an autoimmune serum directed against human lamins A and C (LSI), also label these bands, suggesting they are related to the intermediate filament/lamin family. IFA, another intermediate filament antibody, labels a band at approximately 60×103Mr which is also enriched in the urea extracts of nuclear matrices. Immunofluorescence microscopy with JIM 63, ME 101, AFB and LSI shows network-like staining, often extending around the nucleolus. In many cases the staining reveals structures that appear to be bundles of fibres. JIM 63 also shows a weak staining of the nuclear rim in carrot nuclei, which can be greatly enhanced by treatment of the specimen with cold methanol after fixation. JIM 63 cross-reacts with all the other plant species we have tested. Vibratome sections of pea roots, extracted as for nuclear matrix preparation and stained with JIM 63 show a clear, strong nuclear rim labelling. Furthermore, JIM 63 strongly labels the nuclear lamina in rat liver nuclei. We suggest that the 92×103Mr protein(s) are related to intermediate filaments and/or lamins, and are distributed both within the nucleus and at the nuclear periphery.
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