Somatic cell cytology of the chromosome-eliminating, intergeneric hybrid Hordeum vulgare × Psathyrostachys fragilis
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In the hybrid Hordeum vulgare × Psathyrostachys fragilis the two genomes were differentiated (i) by length, the P. fragilis chromosomes being 31% longer than the H. vulgare chromosomes; (ii) by a difference in staining intensity of C-banded chromosomes (of possible use for exact localization of breakpoints), the H. vulgare chromosomes being the more heavily stained; (iii) by widely different C-banding patterns; and (iv) by the difference between N-banded H. vulgare and non-N-banded P. fragilis chromosomes. Only C-banding patterns identified each chromosome. Aneuploid cells had lost between one and five P. fragilis chromosomes. Loss of H. vulgare chromosomes is ascribed to squashing. No haploid H. vulgare cell was observed. The P. fragilis chromosomes were characterized by diminished centric constrictions, suppression of nucleolar constrictions, and nucleolus activity, i.e., differential amphiplasty, and generally a peripheral location on the metaphase plate. The same characteristics are normally observed in hybrids producing haploids H. vulgare, suggesting a common mechanism of chromosome elimination. Some cells had a side-by-side arrangement of genomes. The only effect of the hybrid condition on H. vulgare chromosomes was the formation of wider nucleolar constrictions and larger nucleolus organizer regions (NORs) than in parental H. vulgare, suggesting a compensational mechanism for nucleolus activity. The passage of H. vulgare chromosomes through the hybrid to the dihaploid did not influence chromosomal characteristics.Key words: Hordeum, Psathyrostachys, hybrids, elimination of chromosomes, banding.Keywords:
Hordeum
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This chapter contains section titled: The Importance of Nucleoli and NORs The Ribosomal Genes Silver Staining of NORs and Nucleoli — What does It Mean? The Nucleolus in Interphase What Happens to the Nucleolus During Cell Division? What Else does the Nucleolus Do?
Interphase
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Nucleolus differentiates around the nucleolus organizer regions of the chromosomes or NORs. In the interphasic nucleoli the fibrillar centers are now considered as the NORs. The purpose of this editorial is to review the experimental data which allowed such identification. Our current concepts regarding this point result from three lines of evidence: 1) specific localization during nucleologenesis, 2) in situ hybridization with labeled ribosomal RNA or DNA, and 3) specific staining with silver.
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Interphase
Secondary constriction
Lymphoblast
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Silver stain
Nucleolar Organizer Region
Ribosomal protein
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Twenty-eight canine mammary tumors were evaluated for histopathologic classification as recommended by the World Health Organization and silver-binding nucleolar organizer region (AgNOR) and nucleolus counts. Samples of surgically excised tumors and tumors taken at necropsy were fixed in neutral formalin, embedded in paraffin, and cut into 1-3-microns-thick sections. Two sections were taken from each tumor: one was stained with hematoxylin and the other was treated with the silver staining technique for the demonstration of AgNORs. After histopathologic classification, the number of nucleoli and the number of AgNORs/nucleus and AgNORs/nucleolus were determined. Statistical analysis (Student's t-test) showed a significant difference in the mean number of nucleoli (P < 0.005), mean number of AgNORs/nucleolus (P < 0.001), and mean number of AgNORs/nucleus (P < 0.005) between benign and malignant canine mammary tumors. There was no significant differences between metastatic and nonmetastatic malignant tumors.
Silver stain
Statistical Analysis
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The main maturation stages of Norway rat megakaryocytic series, megakaryoblasts and mature megakaryocytes, stained by silver for demonstration of argyrophil nucleolus organizer regions (AgNORs) were investigated to provide basic information on the number of nucleoli and interphasic AgNORs in these cells. The results showed that megakaryoblasts as well as mature megakaryocytes possess numerous nucleoli; their number and also the number of AgNORs is significantly higher in less mature than in more mature cells. The number of AgNORs in megakaryocytes of the Norway rat and man are virtually the same, although the numbers of nucleolar organizers per haploid chromosome set differ markedly. This fact leads to the conclusion that the number of interphasic AgNORs depends on the function and metabolic state of the cell rather than on the number of nucleolar organizers.
Nucleolar Organizer Region
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Secondary constriction
Dominance (genetics)
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Hordeum
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Hordeum
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