Reverse heteropyknosis between euchromatin and heterochromatin of the X chromosome in meiotic prophase of the cockroach Blaberus discoidalis

1983 ◽  
Vol 25 (1) ◽  
pp. 72-75
Author(s):  
Liming Shi ◽  
T. C. Hsu ◽  
Sen Pathak

The X chromosome and all autosomes of the cockroach Blaberus discoidalis (2n = 37, XO) contain large segments of constitutive heterochromatin (C-bands). From spermatogonial metaphases, the C-bands are found to be located in the middle of most chromosomes, including the X. The C-bands show bright fluorescence when stained with Hoechst 33258. In pachytene, autosomal heterochromatin can be easily identified in acetic orcein squash preparations as condensed segments. In the same preparations the X chromosome exhibits a "closed" appearance with a lightly stained middle loop and two heavily stained terminal segments which lie side-by-side as if they are paired. In C-banded preparations, an opposite reaction is found, i.e., the loop is heavily stained while the tips are lightly stained. In Hoechst 33258 preparations, the loop is brightly fluorescent while the tips are less brightly stained. Thus, in pachytene of conventional orcein preparations the heteropyknotic behavior between euchromatin and heterochromatin of the X chromosome is the reverse of the usual staining pattern; instead of condensed heterochromatin and decondensed euchromatin, euchromatin is condensed whereas heterochromatin is decondensed. The "paired" euchromatic tips may suggest autologous homology between the original X and the original Y which might have been translocated onto the X in the course of karyological evolution.

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.


1984 ◽  
Vol 62 (2) ◽  
pp. 190-192 ◽  
Author(s):  
Martin L. Adamson ◽  
Daniel Van Waerebeke

Certain cytological aspects of gametogenesis are examined in two species of rhigonematid nematodes parasitizing the posterior gut of Anadenobolus politus (Rhinocricidae; Diplopoda) in Guadeloupe. In both species, sex is determined by an XX/XO mechanism; this is taken as an indication of the phylogenetic distinctness of rhigonematids from the order Oxyurida which recent studies show to be haplodiploid. In Ichthyocephalus anadenoboli. males had 9 and females had 10 chromosomes; in Heth mauriesi, males had 15 and females had 16 chromosomes. In both species, the X chromosome and one autosomal pair were positively heteropyenotic (i.e., they condensed before and stained more intensely than the rest of the chromosomes) during meiotic prophase in males; in H. mauriesi, these chromosomes were negatively heteropyenotic during meiotic metaphase in males. In females of both species, all chromosomes stained similarly.


1977 ◽  
Vol 19 (3) ◽  
pp. 537-541 ◽  
Author(s):  
J. E. K. Cooper

The distribution of constitutive heterochromatin has been examined by C-banding in two somatic cell lines, grown in vitro, from a female Microtus agrestis. One line retains one intact X chromosome together with the short arm of the other X chromosome, while the other cell line retains only the short arm of one X chromosome. Thus, each cell line has lost substantial amounts of heterochromatin from the sex chromosomes, but this material has been deleted from the cells, and not translocated to other chromosomes. Nonetheless, both cell lines continue to propagate well in vitro.


Genetics ◽  
1981 ◽  
Vol 98 (3) ◽  
pp. 529-548
Author(s):  
James A Kennison

ABSTRACT Cytological and genetic analyses of 121 translocations between the Y chromosome and the centric heterochromatin of the X chromosome have been used to define and localize six regions on the Y chromosome of Drosophila melanogaster necessary for male fertility. These regions are associated with nonfluorescent blocks of the Y chromosome, as revealed using Hoechst 33258 or quinacrine staining. Each region appears to contain but one functional unit, as defined by failure of complementation among translocations with breakpoints within the same block. The distribution of translocation breakpoints examined appears to be nonrandom, in that breaks occur preferentially in the nonfluorescent blocks and not in the large fluorescent blocks.


2000 ◽  
Vol 23 (3) ◽  
pp. 595-599 ◽  
Author(s):  
Luís R.R. Rodrigues ◽  
Regina M.S. Barros ◽  
Maria de Fátima L. Assis ◽  
Suely A. Marques-Aguiar ◽  
Julio C. Pieczarka ◽  
...  

The karyotypes of Phyllostomus discolor and P. hastatus from Eastern Amazonia were studied by G-, C-, G/C sequential and Ag-NOR techniques. Both species presented 2n = 32, with the autosome complement composed of 30 bi-armed in P. discolor and 28 bi-armed plus 1 acrocentric in P. hastatus. In both species, the X chromosome is medium submetacentric while the Y is minute acrocentric. The present study found only one difference between the karyotypes of P. discolor and P. hastatus: the smallest autosome (pair 15) is bi-armed in discolor and acrocentric in hastatus, a result best explained by pericentric inversion. The C-banding revealed constitutive heterochromatin only at the centromeric regions of all chromosomes, with the NOR site located at the distal region of short arm of pair 15, in both species. The taxon P. discolor is considered primitive for genus Phyllostomus and the bi-armed form of pair 15 is the assumed primitive condition which, rearranged by a pericentric inversion originated the acrocentric from found in P. hastatus.


1981 ◽  
Vol 37 (3) ◽  
pp. 317-322 ◽  
Author(s):  
P. G. Johnston

SUMMARYThe expression of X-linked phosphoglycerate kinase (PGK-1) in germ cells from embryos heterozygous for both PGK-1 and Searle's translocation T(X; 16) 16H was examined to investigate X chromosome activity during oogenesis. The Pgk-lb allele on the translocated X chromosome was the only allele active in somatic cells of all embryos and in germ cells from 12·5 d.p.c. embryos. However, an additional faint band representing Pgk-la activity was observed in germ cells from older embryos (13·5–18·5 d.p.c.) and neonates (1–2 d.p.p.). It is concluded that there is a period when only one X chromosome is active in early female germ cells and that reactivation of the inactive X chromosome takes place just prior to meiotic prophase.


1976 ◽  
Vol 18 (3) ◽  
pp. 513-518 ◽  
Author(s):  
M. Manolache ◽  
W. M. Ross ◽  
M. Schmid

The chromosomes of the domestic dog (Beagle) were investigated by several different staining techniques. G-banding, Q-banding, and the bis-benzimidazol derivative Hoechst 33258, make possible the identification of all 39 chromosome pairs. Constitutive heterochromatin (C-bands) was present on a few chromosomes as distinctive, large stained areas; on the other autosomes there was little or no heterochromatin detectable.


Reproduction ◽  
2007 ◽  
Vol 133 (5) ◽  
pp. 899-907 ◽  
Author(s):  
P Robles ◽  
I Roig ◽  
R Garcia ◽  
A Ortega ◽  
J Egozcue ◽  
...  

Only little is known about the meiotic prophase events in human oocytes, although some of them are involved in the origin of aneuploidies. Here, a broad study of the pairing and synaptic processes in 3263 human euploid and 2613 aneuploid oocytes (47,XX, +21 and 47,XX, +13), using different techniques and methods, is presented in order to elucidate the characteristics of this essential meiotic process. Our results reaffirm the existence of a common high efficiency in the pairing process leading to the obtainment of a bivalent for all chromosomes studied in euploid and aneuploid cases. Nevertheless, this high efficiency was insufficient to consistently produce trivalents in aneuploid oocytes. Trivalent 21 was only observed in 48.8% of the 47,XX, +21 pachytene-stage oocytes studied, and trivalent 13 was found in 68.7% of the 47,XX, +13 pachytene-stage oocytes analyzed. Our data confirm the hypothesis which suggests that in human oocytes the presence of an extra chromosome could interfere in bouquet dynamics. In addition, the pairing process of the X chromosome is altered in trisomic 21 oocytes, providing evidence of the influence that an extra chromosome 21 may cause meiotic progression.


Genetics ◽  
1982 ◽  
Vol 102 (4) ◽  
pp. 795-806
Author(s):  
Baldev K Vig

ABSTRACT The late metaphase-early anaphase cells from various tissues of male Mus musculus, M. poschiavinus, M. spretus, M. castaneus, female and male Bos taurus (cattle) and female Myopus schisticolor (wood lemming) were analyzed for centromeres that showed separation into two daughter centromeres and those that did not show such separation. In all strains and species of mouse the Y chromosome is the first one to separate, as is the X or Y in the cattle. These sex chromosomes are devoid of constitutive heterochromatin, whereas all autosomes in these species carry detectable quantities. In cattle, the late replicating X chromosome appears to separate later than the active X. In the wood lemming the three pairs of autosomes with the least amount of centromeric constitutive heterochromatin separate first. These are followed by the separation of seven pairs of autosomes carrying medium amounts of constitutive heterochromatin. Five pairs of autosomes with the largest amounts of constitutive heterochromatin are the last in the sequence of separation. The sex chromosomes with medium amounts of constitutive heterochromatin around the centromere, and a very large amount of distal heterochromatin, separate among the very late ones but are not the last. These observations assign a specific role to centromeric constitutive heterochromatin and also indicate that nonproximal heterochromatin does not exert control over the sequence in which the centromeres in the genome separate. It appears that qualitative differences among various types of constitutive heterochromatin are as important as quantitative differences in controlling the separation of centromeres.


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