Silver staining of histone-depleted metaphase chromosomes

1983 ◽  
Vol 147 (2) ◽  
pp. 287-296 ◽  
Author(s):  
G BURKHOLDER
1978 ◽  
Vol 20 (3) ◽  
pp. 377-382 ◽  
Author(s):  
Patricia A. Martin-Deleon ◽  
Dorene L. Petrosky ◽  
M. Eileen Fleming

Nucleolar organizer regions (NOR's) were demonstrated in metaphase chromosomes of the domestic rabbit, Oryctolagus cuniculus (L.) (New Zealand white strain) using silver staining. Sequential quinacrine banding and a modification of the Ag-AS silver precipitation technique with duplicate photography allowed identification of silver staining NOR's on the short arms of chromosomes 13, 16, and 20, as well as the telomeric region of the long arms of number 21 in some cells. Chromosomes 13, 16 and 20 all have subterminal to terminal centromeres, often showed satellites and secondary constrictions, and were sometimes involved in associations.


1982 ◽  
Vol 141 (1) ◽  
pp. 117-125 ◽  
Author(s):  
Huai-Zu Zheng ◽  
Gary D. Burkholder

2002 ◽  
Vol 115 (14) ◽  
pp. 2839-2846
Author(s):  
Ana D. Caperta ◽  
Nuno Neves ◽  
Leonor Morais-Cecílio ◽  
Rui Malhó ◽  
Wanda Viegas

The standard rye cultivar `Imperial' and a structural variant carrying an intact 1R chromosome and two telocentric 1R chromosomes (short and long arms)were used to investigate expression patterns of homologous rDNA loci, and the influence of chromosome structural change on their interphase organisation and relative disposition. Sequential silver staining and in situ hybridization with the rDNA probe pTa71, established a correspondence between the expression and organization patterns of rDNA domains in metaphase and interphase cells. In most cells of the cultivar Imperial, nucleolar organizer region (NOR)silver staining on metaphase chromosomes with equivalent numbers of rDNA genes revealed a size heteromorphism between homologous rDNA loci, resulting from their differential expression. NOR heteromorphism in the structural variant line was significantly reduced. The preferential activity of one NOR over its homologue was found to be random within cells and independent of parental origin. Nucleotypic modifications mediated by changes in the 1R chromosome structure include increased proximity between homologous rDNA loci in interphase, and an increase in the frequency of cells with intra-nucleolar ribosomal condensed chromatin. These results seem to indicate a `sequence recognition' process for the regulation of homologous loci.


1984 ◽  
Vol 26 (2) ◽  
pp. 141-145 ◽  
Author(s):  
D. G. Bedo

The karyotype of Phthorimaea operculella is similar in both sexes and consists of 29 chromosome pairs. These are of similar size with gradual intergradation except for one pair which is significantly longer. C-banding and fluorescent staining with quinacrine and Hoechst 33258 failed to induce bands in metaphase chromosomes while silver staining clearly showed active nucleoli in all stages except metaphase. The banding results are compared with the few reports available on banding of holocentric chromosomes. It is concluded that considerable variability exists in the heterochromatic structure of holocentric chromosomes.Key words: Lepidoptera, moth, karyotype, C-banding.


Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 900-908 ◽  
Author(s):  
Stephen M. Stack

A new technique called salt-nylon silver staining has been used to stain cores in the chromosomes of Lilium longiflorum. Cores are visible in both mitotic and meiotic chromosomes. In C-metaphase chromosomes, a thin core is coiled to form a thick core in each chromatid. In early prophase I of meiosis, silver-stained axial cores and synaptonemal complexes show no indication of coiling before their disappearance in early diplotene. In diakinesis, pairs of thin cores reappear in large major coils. These cores can be seen to cross over between homologous chromosomes. By metaphase I, thin cores coil to form thick cores, which themselves spiral in major coils. The most striking appearance of the cores occurs during anaphase I, when homologous chromosomes separate and sister chromatids swing apart to display thick cores in major coils. During meiosis II cores are in minor coils embedded in elongate chromosomes that show relic major coiling. These observations indicate that plant chromosomes have silver-stainable cores that are comparable with cores that have been reported in the chromosomes of mammals and grasshoppers.Key words: chromosome cores, silver staining, mitosis, meiosis, plants.


1972 ◽  
Vol 21 (1-2) ◽  
pp. 139-142 ◽  
Author(s):  
Mihály Bartalos ◽  
John D. Rainer

SummaryThe application of an ammoniacal silver procedure to the staining of human metaphase chromosomes is described. A map based on the differential staining characteristics of chromosome segments is presented.


1995 ◽  
Vol 131 (1) ◽  
pp. 7-17 ◽  
Author(s):  
J F Giménez-Abián ◽  
D J Clarke ◽  
A M Mullinger ◽  
C S Downes ◽  
R T Johnson

Metaphase chromatids are believed to consist of loops of chromatin anchored to a central scaffold, of which a major component is the decatenatory enzyme DNA topoisomerase II. Silver impregnation selectively stains an axial element of metaphase and anaphase chromatids; but we find that in earlier stages of mitosis, silver staining reveals an initially single, folded midline structure, which separates at prometaphase to form two chromatid axes. Inhibition of topoisomerase II prevents this separation, and also prevents the contraction of chromatids that occurs when metaphase is arrested. Immunolocalization of topoisomerase II alpha reveals chromatid cores analogous to those seen with silver staining. We conclude that the chromatid cores in early mitosis form a single structure, constrained by DNA catenations, which must separate before metaphase chromatids can be resolved.


Genome ◽  
1989 ◽  
Vol 32 (3) ◽  
pp. 380-382 ◽  
Author(s):  
Philip D. Sudman ◽  
Ira F. Greenbaum

Brief staining with AgNO3 was found to differentially stain the kinetochores of chromosomes from diakinesis – metaphase I and metaphase II nuclei of mammals. The results differ from those of Giemsa-stained or C-banded preparations as the silver-stained meiotic kinetochores are clearly distinguishable from both constitutive heterochromatin and euchromatin. Silver-staining is presented as a valuable method for the staining of meiotic material because it allows for the positive identification of centromeric position and orientation with respect to chiasmata. The nonargentophilic nature of the centromere (kinetochore) region of spermatogonial metaphase chromosomes in some species suggests a fundamental structural difference between mitotic and meiotic kinetochores.Key words: kinetochore, meiosis, mammal.


Author(s):  
Kazuaki Misugi ◽  
Nobuko Misugi ◽  
Hiroshi Yamada

The authors had described the fine structure of a type of pancreatic islet cell, which appeared different from typical alpha and beta cells, and tentatively considered that this third type of granular cell probably represents the D cell (Figure 1).Since silver staining has been widely used to differentiate different types of pancreatic islet cells by light microscopy, an attempt to examine this staining reaction at the electron microscopic level was made.Material and Method: Surgically removed specimens from three infants who suffered from severe hypoglycemia were used. The specimens were fixed and preserved in 20% neutral formalin. Frozen sections, 30 to 40 micron thick, were prepared and they were stained by Bielschowsky's method as modified by Suzuki (2). The stained sections were examined under a microscope and islet tissues were isolated. They were fixed in 1% osmium tetroxide in phosphate buffer for one hour and embedded in Epon 812 following dehydration through a series of alcohols and propylene oxide.


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