Changes in NOR activity pattern in the presence of supernumerary heterochromatin in the grasshopper Eyprepocnemis plorans

Genome ◽  
1995 ◽  
Vol 38 (1) ◽  
pp. 68-74 ◽  
Author(s):  
M. D. López-León ◽  
J. Cabrero ◽  
J. P. M. Camacho

Nucleolus organizer region (NOR) activity was analysed in four types of males of the grasshopper Eyprepocnemis plorans, possessing two kinds of supernumerary heterochromatin: a B chromosome and a supernumerary chromosome segment proximally located on the smallest autosome (S11). In males lacking extra heterochromatin, the four active NORs located on the S9, S10, S11, and X chromosomes showed independent activity patterns, but several kinds of dependence appeared in the presence of supernumerary heterochromatin. Furthermore, temporal changes in NOR activity were observed during the first 2 weeks of adult life in standard males but not in males carrying supernumerary heterochromatin. It is suggested that all these effects are related to the DNA content of both types of extra heterochromatin.Key words: NOR, supernumerary heterochromatin, grasshopper, Eyprepocnemis plorans.

Genome ◽  
1987 ◽  
Vol 29 (1) ◽  
pp. 116-121 ◽  
Author(s):  
J. Cabrero ◽  
J. D. Alché ◽  
J. P. M. Camacho

Four nucleolar organizer regions (NORs) are active in standard males of the grasshopper Eyprepocnemis plorans. They are located near the centromeric regions of the S9, S10, S11, and X chromosomes. Changes in the pattern of NOR activity have been observed in the presence of a B2 type supernumerary chromosome. Males with one B show a higher mean number of active NORs per cell than do zero B males owing to significant increases in the activity of the NORs on the S11 and the X. Zero B and one B embryos, however, showed similar patterns of activity. In a male carrying a centric fusion between a B and one of the L1 chromosomes, the activation of a latent NOR, present at the telomere of the long arm of the B, parallelled a significant decrease of NOR activity on the S9 and S10 bivalents stemming from a competition between different NORs in the presence of the B. Thus, while in zero B males the activity of the S10 NOR influences that of the NORs on the X and S9 in a negative way, in one B males it does not do so, although such an influence is observed in the B–L1 fusion male where the activity of the S10 NOR again decreases significantly. On the other hand, the activities of the NORs on the S9 and S11 show a significant positive interdependence in both zero B and one B males where S11 NOR activity is increased but do not do so in the B–L1 fusion male, which shows a significant decrease in the S9 NOR activity. Key words: Eyprepocnemis plorans, B chromosome, nucleolus.


Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 157-161 ◽  
Author(s):  
Kent M. Reed

Paternal sex ratio (PSR) is a B chromosome found in the parasitic wasp Nasonia vitripennis. PSR has a unique etiology in that it destroys the paternal chromosomes of fertilized eggs, resulting in the production of all male families. This study examined structural aspects of PSR including size, C-banding, and silver staining. PSR was found to constitute approximately 5.7% of the genome of carrier males. C-banding confirmed the heterochromatic nature of PSR and the data suggest that PSR remains primarily condensed throughout the cell cycle. Examination of prometaphase spermatocytes revealed a secondary constriction on PSR. The constriction, however, did not stain positive for nucleolus organizer activity. During mitosis, PSR and the pericentromeric regions of the A chromosomes displayed a temporal pattern of silver staining, involving dense precipitation of silver prior to metaphase. This reaction is indicative of a protein complex specific to the heterochromatin of these regions. The implications of these findings to the origin of PSR are discussed.Key words: Nasonia vitripennis, paternal sex ratio, B chromosome, nucleolus organizer region, heterochromatin.


Chromosoma ◽  
1991 ◽  
Vol 100 (2) ◽  
pp. 134-138 ◽  
Author(s):  
M. D. L�pez-Le�n ◽  
J. Cabrero ◽  
J. P. M. Camacho

1996 ◽  
Vol 250 (1) ◽  
pp. 123-128
Author(s):  
Georg Haberer ◽  
Thilo C. Fischer ◽  
Ramón A. Torres-Ruiz

Science ◽  
1979 ◽  
Vol 205 (4403) ◽  
pp. 308-310 ◽  
Author(s):  
RH Myers ◽  
DA Shafer

The serendipitous mating of a male gibbon, Hylobates moloch, and a female siamang, Symphalangus syndactylus, has produced two female offspring born 1 year apart. The hybrid karyotype of 47 chromosomes comprises the haploid complements of the parental species, 22 for the gibbon and 25 for the siamang. Chromosomal G and C banding comparisons revealed no clear homologies between the parental karyotypes except for the single chromosome in each species containing the nucleolus organizer region. The lack of homology suggests that the structural rearrangement of chromosomes has played a major role in the process of speciation for these lesser apes.


1988 ◽  
Vol 51 (2) ◽  
pp. 103-109 ◽  
Author(s):  
Jennifer A. Marshall Graves ◽  
Garey W. Dawson

SummaryIn marsupials, X chromosome inactivation is paternal and incomplete. The tissue-specific pattern of inactivation of X-linked loci (G6PD, PGK, GLA) has been attributed to a piecemeal inactivation of different regions of the X. We here propose an alternative hypothesis, in which inactivation of the marsupial X is a chromosome-wide event, but is differentially regulated in different tissues. This hypothesis was suggested by the relationship between the positions and activity of genes on the kangaroo paternal X. In the absence of an HPRT polymorphism, we have used somatic cell hybridization to assess the activity of the paternal HPRT allele in lymphocytes and fibroblasts. The absence of the paternal X, and of the paternal forms of G6PD or PGK, from 33 cell hybrids made by fusing HPRT-deficient rodent cells with lymphocytes or fibroblasts of heterozygous females, suggests that the HPRT gene on the paternal X is inactive in both tissues and therefore not selectable. Since HPRT is located medially on the Xq near GLA, which shares the same characteristics of activity, we suggest that the locus-specific and tissue-specific patterns of activity result from a differential spread of inactivation from a single control locus, located near HPRT and GLA, outwards in both directions to G6PD and PGK. The nucleolus organizer region on the short arm does not seem to be part of the inactivated unit.


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