Martínez-Expósito M J, Méndez J, Pasantes J J
Dpto. Bioloxía Fundamental, Xenética, Universidade de Vigo, Spain.
Chromosome Res. 1997 Jun;5(4):268-73. doi: 10.1023/a:1018475804613.
The chromosomes of the mussel Mytilus galloprovincialis were analysed by means of chromomycin A3 (CMA), distamycin A/DAPI (DA/DAPI), DAPI/actinomycin D (DAPI/AMD) and chromomycin A3/distamycin A/DAPI (CDD) fluorescence banding techniques, C-banding, silver staining, N-banding and in situ hybridization with 18S+28S rDNA and telomere probes. 18S+28S rDNA clusters were located on the telomeres of two pairs of submeta/subtelocentric chromosomes. The nucleolar organizing regions (NORs) were associated with bright CMA fluorescence, dull DAPI fluorescence and C- and N-positive bands, but not all four NOR-associated heterochromatin bands showed bright CMA fluorescence in a given cell; intra- and interindividual variability was found in this character. Additional non-ribosomal C-bands did not show any differential fluorescent behaviour.
采用放线菌素A3(CMA)、偏端霉素A/4,6-二脒基-2-苯基吲哚(DA/DAPI)、4,6-二脒基-2-苯基吲哚/放线菌素D(DAPI/AMD)和放线菌素A3/偏端霉素A/4,6-二脒基-2-苯基吲哚(CDD)荧光显带技术、C显带、银染、N显带以及用18S + 28S核糖体DNA和端粒探针进行原位杂交,对地中海贻贝的染色体进行了分析。18S + 28S核糖体DNA簇位于两对亚中/亚端着丝粒染色体的端粒上。核仁组织区(NORs)与明亮的CMA荧光、暗淡的DAPI荧光以及C和N阳性带相关,但在给定细胞中并非所有四个与NOR相关的异染色质带都显示明亮的CMA荧光;在这一特征中发现了个体内和个体间的变异性。额外的非核糖体C带未显示任何差异荧光行为。