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Different chromatin fractions of tomato (Solanum lycopersicum L.) and related species
Authors:AC Brasileiro-Vidal  MB Melo-Oliveira  GMG Carvalheira  M Guerra
Institution:aDepartment of Genetics, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n Cidade, 50670-901 Recife, PE, Brazil;bDepartment of Biochemistry, Federal University of Pernambuco (UFPE), 50670-901 Recife, PE, Brazil;cDepartment of Biology, Rural Federal University of Pernambuco (UFRPE), 52171-900 Recife, PE, Brazil;dDepartment of Botany, Federal University of Pernambuco (UFPE), 50670-901 Recife, PE, Brazil
Abstract:Conventional chromosome staining has suggested that more than 75% of the tomato chromosomes are constituted by heterochromatin. In order to determine whether more deeply stained proximal regions are classic heterochromatin, the distributions of C-bands and chromomycin A3 (CMA) bands, and the prophase condensation patterns, were analysed in tomato. In this and most other species of the tomato clade, the 5S and 45S rDNA sites were also localised. In tomato, CMA banding was similar to C-banding. After conventional staining, all species displayed large condensed heteropycnotic regions that did not correspond to C-bands or CMA bands. Analyses of the CMA banded karyotypes revealed a low heterochromatin content. Around 12–17% of the chromatin of tomato was CMA+ and 1/4 to 1/5 of this heterochromatin corresponded to 45S rDNA. In other species, the CMA+ heterochromatin showed extensive variation (8–35%), but was never near the values found in the literature for tomato. These data suggest the existence of three principal fractions of chromatin in tomato and related species: the late condensed euchromatin corresponding to the terminal regions of the chromosomes, the precocious condensed euchromatin that occupies the major part of the chromosomes and the constitutive heterochromatin that represents those regions revealed by C-bands.
Keywords:CMA  5S and 45S rDNA  FISH  Heterochromatin  Solanaceae
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