We report the karyotype characteristics including chromosome numbers of Saga campbelli campbelli, S. c. gracilis, and S. rammei using the following classical cytogenetic methods: C-banding, silver staining, and fluorochrome staining DAPI and CMA3. We also present FISH data showing the distribution of telomeric repeats and 18S rDNA on the chromosomes of these species and the results of similar studies cited in the literature on S. hellenica, S. natoliae, and S. rhodiensis. The five European Saga species exhibit a high rate of karyotype evolution. In addition to changes in chromosome number and morphology (by chromosomal inversion and/or chromosome fusion), interspecific autosomal differentiation involved changes in the distribution and quantity of constitutive heterochromatin and GC-rich regions, as well as the number and location of NORs. In the present study we focused on testing a hypothetical model of karyotype evolution in Saga, with particular reference to the cytogenetic mapping of rDNA and telomeric sequences. Variation in the distribution of rDNA and location of Ag-NORs are novel phylogenetic markers for the genus Saga.
A cytogenetic investigation was performed in eight species of the spittlebug genus Philaenus using silver-NOR (AgNOR)-banding and fluorescence in situ hybridization (FISH) with 18S rDNA and (TTAGG)n telomeric probes. This is the first application of FISH technique in the Auchenorrhyncha, a suborder of the Hemiptera. FISH along with the rDNA probe revealed differences between species in the number and chromosomal location of major ribosomal RNA gene sites, the so-called nucleolar organizer regions (NORs). However, we found a lack of perfect correlation between the results of AgNOR-staining and rDNA-FISH in the detection of NORs. FISH with the telomeric probe confirmed that the chromosome ends of the Philaenus species are composed of the (TTAGG)n nucleotide sequence, which is a common motif of insect telomeres., Anna Maryanska-Nadachowska, Valetnina G. Kuznetsova, Tatyana V. Karamysheva., and Obsahuje seznam literatury
The present study focused on the evolution of the karyotype in 21 taxa of the genus Isophya, which was done by mapping the location on the chromosomes of ribosomal RNA (rRNA) coding genes using fluorescence in situ hybridization (FISH) with an 18S rDNA probe and using silver staining (AgNO3) to evaluate the activity of major rDNA clusters. Since the chromosome number and sex determination do not vary in this genus, the above markers were used in a detailed comparison of the cytogenetic features of species of Isophya. The species analyzed were placed into three groups based on the location of rDNA on their chromosomes: (1) rDNA-FISH signals only on the two long pairs of autosomes, (2) rDNA-FISH signals on one long and one short pair of autosomes, and (3) rDNA-FISH signals on three to five different sized pairs of autosomes. These groupings partly correspond to the morphological groupings proposed in earlier studies. One long pair of autosomes frequently carried rDNA in all the Isophya species and probably is a plesiomorphic character for these taxa. The cytogenetic mapping revealed great variability among Isophya species in the chromosomal location of major rDNA clusters. Our results suggest that the observed variation in the number of rDNA clusters can be an important species-group specific phylogenetic marker. Analysis of 18S rDNA hybridization signals showed that the evolutionary dynamics of rDNA in this genus is remarkably high and accompanied by changes in the structure of chromosomes bearing rDNA at an inter- and intra-specific level. The telomeric sequence (TTAGG)n hybridized with the termini of most of chromosomes, however, some chromosome ends lacked signals probably due to a low copy number of telomeric repeats. and Beata Grzywacz, Anna Maryańska-Nadachowska, Dragan P. Chobanov, Tatjana Karamysheva, Elżbieta Warchałowska-Śliwa.
Diachasmimorpha longicaudata (Hymenoptera: Braconidae) is a parasitoid wasp widely used in the biological control of fruit flies. In this paper, we present a detailed analysis of the karyotype of this species based on the results of classical and molecular cytogenetic techniques. The cytogenetic analysis confirmed the male and female chromosome numbers previously reported (n = 20, 2n = 40). The entire short arm of most chromosomes is made up of a large constitutive heterochromatic segment. The high heterochromatin content differentiates D. longicaudata from other braconid species. Fluorescence in situ hybridization (FISH) using autologous 18S rDNA probes revealed six clusters of rDNA, i.e. six nucleolar organizer regions (NORs), in the heterochromatic short arms of different chromosomes in the haploid male karyotype. This number is exceptionally high for Hymenoptera, which usually have two NORs in the diploid complement. It is noteworthy that these rDNA-FISH experiments represent the first use of this technique on a braconid species using autologous probes. Since Ag-NOR-bands were coincident with C-positive bands on metaphase chromosomes, it was not possible to identify active nucleoli. The physical characteristics of the D. longicaudata karyotype, especially the content and distribution of heterochromatin and the number and location of rDNA clusters, contribute to a better understanding of the structure and organization of braconid chromosomes and provide a basis for genomic and evolutionary studies., Leonela Carabajal Paladino ... [et al.]., and Obsahuje seznam literatury
The present paper reports some cytogenetic peculiarities observed in the Ag-NORs of Pamphagus ortolaniae chromosomes, the unusual behaviour of ribosomal sites after silver staining and the intense Ag-positive reaction of centromeric regions at spermatogonial metaphase and spermatocyte metaphase I and II. Moreover, a conclusive identification and localization of all the ribosomal clusters is provided by using heterologous rDNA FISH on spermatocyte chromosomes. 18S-28S rDNA mapped on a single chromosome pair and resulted multiclustered along the chromosomal body in three distinct serial regions, r1, r2 and r3. Surprisingly, these areas were scarcely (r1) or never (r2 and r3) detectable by silver impregnation. As in other Orthoptera and many groups of arthropods, FISH with the pentamer (TTAGG)n as the probe labelled the telomeres of all chromosomes.