Chromosome Location of Active Ribosomal Genes inPleurodema Thaul(Amphibia-Leptodactylidae). C-Banding and Polymorphism of The Nucleolar Organizer Region

Caryologia ◽  
1987 ◽  
Vol 40 (4) ◽  
pp. 359-368 ◽  
Author(s):  
Alberto Veloso ◽  
Patricia Iturra
Genetics ◽  
1975 ◽  
Vol 80 (3) ◽  
pp. 505-518
Author(s):  
Samuel A Ramirez ◽  
John H Sinclair

ABSTRACT Cytogenetic and molecular hybridization techniques were used to examine the arrangement of rRNA genes at the nucleolar organizer region (NOR) of maize. TB-6a stocks involving a reciprocal translocation between a B chromosome and the NOR of chromosome 6 were used. The amount of rDNA in the different stocks used varied from 1.5 to 4 NOR equivalents depending on the number of B6 choromosomes present. Cytological measurements show that the medial break through the NOR results in an equal partitioning of the heterochromatic knob (the NOR) between chromosome 6 and the B chromosome to which it was translocated. DNA-rRNA hybridization experiments show a linear relationship between the amount of rRNA capable of hybridizing with DNA and the number of NOR equivalents present. The data confirm McClintock's conclusion that the heterochromatic knob, rather than the constricted portion, is the true NOR region. Further, they show that the number of ribosomal genes is correlated with the amount of cytologically visible NOR, suggesting a uniform distribution of genes throughout the locus.


Genome ◽  
1989 ◽  
Vol 32 (1) ◽  
pp. 35-39 ◽  
Author(s):  
J. R. López ◽  
M. C. Alvarez ◽  
G. Thode ◽  
G. Martinez

A comparative analysis of conventional C-banded and Ag-NOR karyotypes involving the closely related labrid species Symphodus melops and Symphodus roissali showed conspicuous differences between them, reflected mainly in their 2n and fundamental number values. The chromosome rearrangements apparently involved consisted of three centric fusions, pericentric inversions, and (or) translocations, as well as small heterochromatic additions. In spite of this clear divergence, the two species seem to have one larger metacentric pair, the nucleolar organizer region (NOR) carrier chromosomes, and some smaller unidentified pairs in common. Both karyotypes are fully representative of the described tendency in the labrids towards symmetric morphology. The NOR regions were shown to have C-banding and a heteromorphism between homologous regions was detected by conventional and silver staining, but not by the C-banding technique, which leads us to suggest that the NOR regions' heteromorphism is functional rather than structural in nature.Key words: Labridae, heterochromatin, nucleolus organizers.


2021 ◽  
Vol 43 (3) ◽  
pp. 237-249 ◽  
Author(s):  
Thanh Dat Ta ◽  
Nomar Espinosa Waminal ◽  
Thi Hong Nguyen ◽  
Remnyl Joyce Pellerin ◽  
Hyun Hee Kim

Abstract Background DNA tandem repeats (TRs) are often abundant and occupy discrete regions in eukaryotic genomes. These TRs often cause or generate chromosomal rearrangements, which, in turn, drive chromosome evolution and speciation. Tracing the chromosomal distribution of TRs could therefore provide insights into the chromosome dynamics and speciation among closely related taxa. The basic chromosome number in the genus Senna is 2n = 28, but dysploid species like Senna tora have also been observed. Objective To understand the dynamics of these TRs and their impact on S. tora dysploidization. Methods We performed a comparative fluorescence in situ hybridization (FISH) analysis among nine closely related Senna species and compared the chromosomal distribution of these repeats from a cytotaxonomic perspective by using the ITS1-5.8S-ITS2 sequence to infer phylogenetic relationships. Results Of the nine S. tora TRs, two did not show any FISH signal whereas seven TRs showed similar and contrasting patterns to other Senna species. StoTR01_86, which was localized in the pericentromeric regions in all S. tora, but not at the nucleolar organizer region (NOR) site, was colocalized at the NOR site in all species except in S. siamea. StoTR02_7_tel was mostly localized at chromosome termini, but some species had an interstitial telomeric repeat in a few chromosomes. StoTR05_180 was distributed in the subtelomeric region in most species and was highly amplified in the pericentromeric region in some species. StoTR06_159 was either absent or colocalized in the NOR site in some species, and StoIGS_463, which was localized at the NOR site in S. tora, was either absent or localized at the subtelomeric or pericentromeric regions in other species. Conclusions These data suggest that TRs play important roles in S. tora dysploidy and suggest the involvement of 45S rDNA intergenic spacers in “carrying” repeats during genome reshuffling.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jung-Hyun Kim ◽  
Vladimir N. Noskov ◽  
Aleksey Y. Ogurtsov ◽  
Ramaiah Nagaraja ◽  
Nikolai Petrov ◽  
...  

AbstractThe rDNA clusters and flanking sequences on human chromosomes 13, 14, 15, 21 and 22 represent large gaps in the current genomic assembly. The organization and the degree of divergence of the human rDNA units within an individual nucleolar organizer region (NOR) are only partially known. To address this lacuna, we previously applied transformation-associated recombination (TAR) cloning to isolate individual rDNA units from chromosome 21. That approach revealed an unexpectedly high level of heterogeneity in human rDNA, raising the possibility of corresponding variations in ribosome dynamics. We have now applied the same strategy to analyze an entire rDNA array end-to-end from a copy of chromosome 22. Sequencing of TAR isolates provided the entire NOR sequence, including proximal and distal junctions that may be involved in nucleolar function. Comparison of the newly sequenced rDNAs to reference sequence for chromosomes 22 and 21 revealed variants that are shared in human rDNA in individuals from different ethnic groups, many of them at high frequency. Analysis infers comparable intra- and inter-individual divergence of rDNA units on the same and different chromosomes, supporting the concerted evolution of rDNA units. The results provide a route to investigate further the role of rDNA variation in nucleolar formation and in the empirical associations of nucleoli with pathology.


2005 ◽  
Vol 32 (5) ◽  
pp. 323-328 ◽  
Author(s):  
Rosana F. Romao-Correa ◽  
Durvanei A. Maria ◽  
Mithitaka Soma ◽  
Mirian N. Sotto ◽  
Jose Antonio Sanches ◽  
...  

2016 ◽  
Vol 22 (3) ◽  
pp. 621-629 ◽  
Author(s):  
Tomás Nepomuceno-Mejía ◽  
Reyna Lara-Martínez ◽  
Roberto Hernández ◽  
María de Lourdes Segura-Valdez ◽  
Luis F. Jiménez-García

AbstractNucleolar assembly is a cellular event that requires the synthesis and processing of ribosomal RNA, in addition to the participation of pre-nucleolar bodies (PNBs) at the end of mitosis. In mammals and plants, nucleolar biogenesis has been described in detail, but in unicellular eukaryotes it is a poorly understood process. In this study, we used light and electron microscopy cytochemical techniques to investigate the distribution of nucleolar components in the pathway of nucleolus rebuilding during closed cell division in epimastigotes of Trypanosoma cruzi, the etiologic agent of American trypanosomiasis. Silver impregnation specific for nucleolar organizer regions and an ethylenediaminetetraacetic acid regressive procedure to preferentially stain ribonucleoprotein revealed the conservation and dispersion of nucleolar material throughout the nucleoplasm during cell division. Furthermore, at the end of mitosis, the argyrophilic proteins were concentrated in the nucleolar organizer region. Unexpectedly, accumulation of nucleolar material in the form of PNBs was not visualized. We suggest that formation of the nucleolus in epimastigotes of T. cruzi occurs by a process that does not require the concentration of nucleolar material within intermediate nuclear bodies such as mammalian and plant PNBs.


1980 ◽  
Vol 58 (2) ◽  
pp. 164-171 ◽  
Author(s):  
J. C. Semple ◽  
C. C. Chinnappa

The karyotypes of all species of Chrysopsis were analysed and four basic complements were recognised. The X = 5 karyotype was possessed by all seven n = 5 species and consisted of three submetacentric and two acrocentric chromosomes, one bearing the nucleolar organizer region medially on its short arm. Each X = 4 species had a distinct karyotype. The n = 4 karyotype of C. mariana had diverged less from the X = 5 karyotype than that of C. pilosa. The X2 = 9 karyotype shared by three n = 9 taxa was found to be little more than a combination of the X = 5 karyotype and the X = 4 mariana karyotype and was therefore of allopolyploid origin. Some shifting in the location of the nucleolar organizer region has occurred in each group.


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