G and/or C-bands in plant chromosomes?

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.

1977 ◽  
Vol 19 (4) ◽  
pp. 739-743 ◽  
Author(s):  
Sheng-Tian Yen ◽  
W. Gary Filion

Modified ASG (Acetic/Saline/Giemsa) and BSG (Barium hydroxide/Saline/Giemsa) chromosome banding techniques applied to several diploid species of oats produced two distinct types of C-banding patterns. One pattern consisted mainly of centromeric bands with occasional telomeric and/or intercalary bands while the other was comprised only of prominent telomeric and intercalary bands. These two banding patterns which probably reflect two distinct types of constitutive heterochromatin resulted from a change in the HCl hydrolysis temperature prior to the application of the ASG or BSG technique; hydrolysis at 60 °C yielded the centromeric bands and hydrolysis at room temperature produced telomeric and intercalary bands. Since all species examined reacted in a similar manner, precise Giemsa banding patterns should now be possible for all or most species of oats.


1984 ◽  
Vol 26 (4) ◽  
pp. 430-435 ◽  
Author(s):  
I. Linde-Laursen ◽  
R. von Bothmer

The karyotype of the outbreeding P. fragilis (2n = 2x = 14) was investigated by Feulgen staining and by C-, N-, and Ag-banding techniques. The complement consisted of 14 large chromosomes, 8 metacentrics and 6 satellite (SAT) chromosomes, probably among the longest within the Poaceae. Two SAT-chromosome pairs carried small, and one pair carried minute, polymorphic, completely heterochromatic satellites. Each chromosome could be referred to one of the seven chromosome pairs by its C-banding pattern. The patterns comprised from zero to three conspicuous, but not large bands per chromosome resulting in an overall low content of constitutive heterochromatin (<4%). The C-banded karyotype of P. fragilis differed from any previously reported in the Triticeae. Six of seven chromosome pairs were polymorphic either for C-banding patterns or satellite size (or for both). N-banding gave no differential staining of chromosomes. Silver nitrate staining established that the nucleolar organizers had different nucleolus-forming capacities. The presence of the small and minute satellites was more consistently demonstrated after C- and N-banding than after Feulgen staining.Key words: Triticeae, Poaceae, karyotype, C-, N-, and Ag-banding.


1986 ◽  
Vol 28 (3) ◽  
pp. 340-347 ◽  
Author(s):  
J. P. Gupta ◽  
Arun Kumar

The distribution of constitutive heterochromatin in mitotic chromosomes of four species (viz., Drosophila quadrilineata de Meijere, D. immigrans Sturtevant, D. pulaua Wheeler, and D. kohkoa Wheeler) was studied using C-banding and fluorescence staining techniques. The results of this study had revealed that the heterochromatic segments detected by C-banding in the species under study were found to coincide precisely with the areas giving bright fluorescence with the two fluorochromes, Hoechst 33258 and quinacrine. This suggested the presence of A–T rich base pairs in their heterochromatin. These studies further revealed that the modification of heterochromatin caused due to the additions or deletions in particular had also played a very significant role during the differentiation of these species.Key words: heterochromatin modification, immigrans species group, Drosophila.


2019 ◽  
Vol 157 (1-2) ◽  
pp. 53-64 ◽  
Author(s):  
Michael Schmid ◽  
Claus Steinlein ◽  
Alina M. Reiter ◽  
Michail Rovatsos ◽  
Marie Altmanová ◽  
...  

An experimental approach using monoclonal anti-5-methylcytosine antibodies and indirect immunofluorescence was elaborated for detecting 5-methylcytosine-rich chromosome regions in reptilian chromosomes. This technique was applied to conventionally prepared mitotic metaphases of 2 turtle species and 12 squamate species from 8 families. The hypermethylation patterns were compared with C-banding patterns obtained by conventional banding techniques. The hypermethylated DNA sequences are species-specific and are located in constitutive heterochromatin. They are highly reproducible and often found in centromeric, pericentromeric, and interstitial positions of the chromosomes. Heterochromatic regions in differentiated sex chromosomes are particularly hypermethylated.


The incidence of C-bands (constitutive heterochromatin), as determined by differential Giemsa staining, was studied in the chromosomes of 56 species, varietal forms and subgenera of Fritillaria and 30 of them are illustrated. With the exception of the subgenera Korolkowi , a supposed link between lilies and fritillaries, the chromosome complements of all plants contained bands. There were wide differences in the size and number of these bands among species both within and between groups. In those with the largest and most abundant bands, there was a pronounced tendency for centromeric localization, both in Old and New World species. The Giemsapositive centromeres were masked when this occurred. Heteromorphy in respect of banding occurred in most species. The relation of repetitive DNA sequences with heterochromatin is discussed, as is also the problem of evolution in Fritillaria .


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.


1983 ◽  
Vol 25 (3) ◽  
pp. 203-209 ◽  
Author(s):  
Ineke Mastenbroek ◽  
J. M. J. de. Wet

An established C-banding technique was modified to consistently yield complete sets of distinct, sharply banded chromosomes in Zea. It was used to demonstrate similarities and differences among heterochromatin patterns of different Zea taxa. The C-banding patterns showed a general agreement with heterochromatic knob positions known from pachytene studies. Two groups of banding patterns could be distinguished. Those taxa with bands that were almost exclusively terminally positioned included Z. mays ssp. parviglumis var. huehuetenangensis, Z. diploperennis, Z. perennis, and Z. luxurians. In the last mentioned, previously unknown heterochromatic regions were found. Both terminal and subterminal band positions were found in Z. mays, Z. mays ssp. mexicana, and Z. mays ssp. parviglumis var. parviglumis. On the basis of these results, and those of other workers, the taxonomic treatments of Z. mays ssp. parviglumis var. huehuetenangensis, and of Z. diploperennis and its autotetraploid derivative Z. perennis are questioned.


1974 ◽  
Vol 14 (3) ◽  
pp. 499-504
Author(s):  
S. M. STACK ◽  
C. R. CLARKE ◽  
W. E. CARY ◽  
J. T. MUFFLY

After the use of different Giemsa staining techniques, variations in chromosome banding patterns have often been observed in animal chromosomes. Such staining differences are usually interpreted to indicate that there is more than one type of heterochromatin in many animal chromosomes. Using two differential Giemsa staining techniques we have found different staining patterns in the chromosomes of two higher plants, Allium cepa and Ornithogalum virens. Furthermore, pericentric heterochromatin that occurs so commonly in animal chromo-somes was specifically Giemsa stained in O. virens. These results suggest the basic similarity of higher plant and animal chromosomes.


Genetics ◽  
1974 ◽  
Vol 78 (2) ◽  
pp. 703-714
Author(s):  
Sen Pathak ◽  
A Dean Stock

ABSTRACT A comparison of the Giemsa-banding patterns of the X chromosomes in various mammalian species including man indicates that two major bands (A and B), which are resistant to trypsin and urea-treatments, are always present irrespective of the gross morphology of the X chromosomes. This is true in all mammalian species with the "original or standard type" X chromosomes (5-6% of the haploid genome) thus far analyzed. In the unusually large-sized X chromosomes the extra chromosomal material may be due either to the addition of genetically inert constitutive heterochromatin or to an X-autosome translocation. In these X chromosomes two major bands are present in the actual X-chromosome segment. Our data on C and G band patterns also support Ohno's hypothesis that the mammalian X chromosome is extremely conservative in its genetic content, in spite of its cytogenetic variability.


1977 ◽  
Vol 19 (4) ◽  
pp. 663-666 ◽  
Author(s):  
H. M. Thomas

A Giemsa staining technique has been applied to the somatic chromosomes of the inbreeding diploid grass Lolium temulentum (2n = 14). Bands appear in six of the seven pairs and are associated either with the centromere or secondary constriction. An idiogram of the chromosomes with their banding patterns is presented.


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