Differential Giemsa staining in plants IV. C-Banding in Avena strigosa

1976 ◽  
Vol 67 (2) ◽  
pp. 117-118 ◽  
Author(s):  
SHENG-TIAN YEN ◽  
W. GARY FILION
1985 ◽  
Vol 27 (3) ◽  
pp. 365-369 ◽  
Author(s):  
April Romagnano ◽  
W. Allan King ◽  
Claude-Lise Richer ◽  
Marie-Antoinette Perrone

A technique is described for the preparation of banded chromosomes from early equine embryos cultured for less than 10 h in a medium containing bromodeoxyuridine. In addition to standard Giemsa staining and C-banding, chromosomes thus prepared can also be R-banded by either the RBA or the RB-FPG methods. This technique is rapid, repeatable, and limits cell loss, making it ideal for the preparation of early embryos.Key words: embryos, chromosomes, banding, horse, cow.


1984 ◽  
Vol 71 (1) ◽  
pp. 111-120
Author(s):  
I. Schubert ◽  
R. Rieger ◽  
P. Dobel

Similarities and differences become evident from comparisons of centromeric and non-centromeric banding patterns in plant and animal chromosomes. Similar to C and G-banding in animals (at least most of the reptiles, birds and mammals), centromeric and nucleolus-organizing region bands as well as interstitially and/or terminally located non-centromeric bands may occur in plants, depending on the kind and strength of pretreatment procedures. The last group of bands may sometimes be subdivided into broad regularly occurring ‘marker’ bands and thinner bands of more variable appearance. Non-centromeric bands in plants often correspond to blocks of constitutive heterochromatin that are rich in simple sequence DNA and sometimes show polymorphism; they thus resemble C-bands. However, most of these bands contain late-replicating DNA. Also they are sometimes rich A X T base-pairs, closely adjacent to each other and positionally identical to Feulgen+ and Q+ bands, thus being comparable to mammalian G-bands. Although banding that is reverse to the non-centromeric bands after Giemsa staining is still uncertain in plants, reverse banding patterns can be obtained with Feulgen or with pairs of A X T versus G X C-specific fluorochromes. It is therefore concluded that not all of the plant Giemsa banding patterns correspond to C-banding of mammalian chromosomes. Before the degree of homology between different Giemsa banding patterns in plants and G and/or C-bands in mammals is finally elucidated, the use of the neutral term ‘Giemsa band’, specified by position (e.g. centromeric, proximal, interstitial, terminal), is suggested to avoid confusion.


2014 ◽  
Vol 57 (3) ◽  
pp. 317-327
Author(s):  
Elżbieta Weryszko-Chmielewska

The number and morphology of <em>Callisia elegans</em> Alexand. chromosomes were studied employing staining with acetic carmine and differential Giemsa staining. It was found that its karyotype was 2n = 12 chromosomes, whose lengths fell in the range of 16.8 to 8.8 µm. The chomosomes, arranged in order of length, were classified respectively to types: sm, t, t, t, t, st. The distribution of C-banding is given for this karyotype. The presence of microsatellites on the long and short arms was found in the chromosomes of the second pair. Frequently there were 4 nucleoli of unequal size in interphase nuclei. In many cells, lower numbers of nucleoli (3-1) were seen which was -probably due to their fusion. The maximum number of nucleoli corresponded to the number of nucleolar organizers accompanying the satellites.


1978 ◽  
Vol 20 (3) ◽  
pp. 307-312 ◽  
Author(s):  
T. Lelley ◽  
K. Josifek ◽  
P. J. Kaltsikes

Extensive polymorphism was found with regard to the presence and size of Giemsa-staining bands in the chromosomes of six inbred lines of cultivated rye (Secale cereale L.). The amount of polymorphism differed from chromosome to chromosome, with 6R being the most variable and 3R or 7R the least.


1979 ◽  
Vol 21 (3) ◽  
pp. 373-378 ◽  
Author(s):  
W. Gary Filion ◽  
David H. Blakey

Somatic metaphase chromosomes of Tulipa which were subjected to various hydrolyses with several times and temperatures displayed two distinctive types of C-banding when stained using the BSG (Barium hydroxide/Saline/Giemsa) chromosome banding technique. In addition to the two types of Giemsa bands, namely intercalary/terminal and centromeric, a unique transition from the former to the latter type of banding was observed. That is, at the point of transition from intercalary/terminal to centromeric banding, both types were present at one time. The two types of Giemsa banding resulted from different HCl hydrolysis times and temperatures; centromeric bands being observed after either a prolonged hydrolysis at room temperature or an increase in the hydrolysis temperature to 60 °C. These results are discussed in relation to the mechanisms of chromosome banding.


1999 ◽  
Vol 22 (3) ◽  
pp. 351-356 ◽  
Author(s):  
Eliana Feldberg ◽  
Jorge Ivan Rebelo Porto ◽  
Elen Bethlen Pedraça dos Santos ◽  
Francisco Carlos Souza Valentim

Cytogenetic characterization of two freshwater sciaenid species from the genus Plagioscion (P. squamosissimus and Plagioscion sp.) was obtained for the first time. Giemsa staining, Ag-NOR and C-banding revealed that both species presented 2n = 48 chromosomes (almost all acrocentric). Single NORs and heterochromatin were found mainly at the pericentromeric position. Karyotypic formulae and NOR location proved to be valuable in showing both interspecific and intraspecific differences. All chromosomes were acrocentric in P. squamosissimus. NORs were located at proximal positions on the long arms of the last chromosome pair of the complement, and were heteromorphic due to size differences. Such heteromorphic NORs seem to be associated with each population sampled. Plagioscion sp. presented two cytotypes: cytotype a (2M + 46A) and cytotype b (48A). In both cytotypes, NOR-bearing chromosomes were located at the proximal position on the long arms of the first chromosome pair of the complement. However, NOR-bearing chromosomes were metacentric in cytotype a and acrocentric in cytotype b.


2012 ◽  
Vol 36 (5) ◽  
pp. 647
Author(s):  
Yan CAI ◽  
Yong-can ZHOU ◽  
Rui-min XIE ◽  
Zhen-yu XIE ◽  
Yong-qin FENG ◽  
...  
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