Giemsa banding patterns of human chromosomes*

2008 ◽  
Vol 3 (3) ◽  
pp. 169-179 ◽  
Author(s):  
Peter E. Crossen
1975 ◽  
Vol 17 (1) ◽  
pp. 81-92 ◽  
Author(s):  
C. C. Lin ◽  
H. van de Sande ◽  
W. K. Smink ◽  
D. R. Newton

Various factors involved in the production of "Q-bands" have been studied. It was found that a Zeiss standard WL fluorescent microscope required a shorter exposure time for photography as compared to a Zeiss photomicroscope. The minimal exposure time was obtained when the standard WL microscope was equipped with a UV light source containing a DC powered mercury burner and a concave mirror. Further, the pH and type of water used in the staining, washing and mounting of the slide were also important factors in producing clear and well differentiated "Q-bands". It also appears that the factors involved in the production of "Q-bands" effect the enhancement or quenching of fluorescence by poly d(A-T).poly d(A-T) and salmon sperm DNA or poly dG∙poly dC respectively. This preliminary report also suggests that DNA or polynucleotides with a specific base sequence may play an important role in Q-banding patterns on chromosomes.


1973 ◽  
Vol 12 (6) ◽  
pp. 377-397 ◽  
Author(s):  
Doris H. Wurster-Hill ◽  
C.W. Gray

1975 ◽  
Vol 14 (1) ◽  
pp. 26-33 ◽  
Author(s):  
G.F. de Vries ◽  
H.F. de France ◽  
J.A.M. Schevers

Genome ◽  
1998 ◽  
Vol 41 (4) ◽  
pp. 616-625 ◽  
Author(s):  
Olga V. Muravenko ◽  
Alexander R. Fedotov ◽  
Elizabeth O. Punina ◽  
Ludmila I. Fedorova ◽  
Valerii G. Grif ◽  
...  

1979 ◽  
Vol 49 (3) ◽  
pp. 291-306 ◽  
Author(s):  
J. J. Yunis ◽  
D. W. Ball ◽  
J. R. Sawyer

1972 ◽  
Vol 11 (2) ◽  
pp. 113-116 ◽  
Author(s):  
B. Dutrillaux ◽  
Catherine Finaz ◽  
J. De Grouchy ◽  
J. Lejeune

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.


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