Different cytogenetic techniques including C-banding, base-specific fluorochromes and silver nitrate staining were used to compare the karyotypes of three species of bugs, representatives of the Neotropical genus Antiteuchus, namely A. mixtus, A. sepulcralis and A. macraspis. The species have holokinetic chromosomes which is typical of the Hemiptera, and their diploid chromosome number is 2n = 14 and they have an XX/XY (female/male) sex chromosome system. C-banding revealed telomeric blocks of constitutive heterochromatin in most chromosomes of these three species. In each species, CMA3-positive blocks were observed in the telomeric heterochromatin region of chromosome pair 1. This chromosome pair carried the nucleolar organizer region (NOR), which silver nitrate staining revealed is located in the telomeric heterochromatin. In contrast to the result obtained with CMA3, entire chromosome complement stained homogenously with DAPI, except for the telomeric region of pair 1, which remained unstained.
The chromosome set of N. anomalus from Bulgaria was studied by means of C-, and NOR-banding. The diploid chromosome number of this species is known to be 2n=52 (NF = 98, NFa = 94). In all the studied individuals, the X chromosome appeared to be the second longest submetacentric chromosome, whereas the Y chromosome was a medium-sized submetacentric chromosome, consisting of heterochromatin. Such morphology of the Y chromosome was not described previously. The extent and localization of C-bands in the pericentromeric regions varied between the pairs of chromosomes. The nucleolar organizer regions (NOR’s) were observed in four pairs of autosomes.
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
Differences in the karyology of two species, Centricnemus leucogrammus and Peritelus familiaris (Coleoptera: Curculionidae), were investigated in order to elucidate their taxonomic position of the taxa. Previously both species were placed in one genus whereas the latest taxonomic revision puts them in separate genera. Cytogenetic analysis of P. familiaris and C. leucogrammus showed significant differences in karyotype structure and confirmed their present taxonomic status. The diploid set of C. leucogrammus consists of 22 chromosomes with a fundamental number of arms (FN) of 45 and little variation in morphology and length. Peritelus familiaris has 24 chromosomes with FN of 47 and a more diverse karyotype. The karyotype evolution might have occured by centric fissions of autosomes. At pachytene and diplotene in spermatocytes, each chromosome bivalent showed a small band of pericentric heterochromatin. The bands were hardly visible or undetectable in other stages of spermatogenesis, namely mitotic metaphase, diakinesis, metaphase I and II. The nucleolar organizer regions (NORs) were active at premeiotic stages and early meiosis, but invisible at meiotic metaphase I, metaphase II, and mitotic metaphase. These results indicate the usefulness of cytogenetic methods in taxonomic evaluations.
The karyotype, C-banding and Ag-NORs of Spermophilus xanthoprymnus (Anatolian souslik) from the Konya in Central Anatolia were examined. The diploid number of chromosomes (2n) is 42, the fundamental number (FN ) is 81, the number of autosomal arms (NFa) is 78. C-banding positive regions appeared to be restricted to the pericentromeric regions in all autosome chromosome pairs and the X chromosome. The relative amount of C-positive heterochromatin is 28.9 % of the total length of the set. Nucleolar organizer regions (NORs), identified by the silver-staining technique, were found on the terminal region of the short arm of three pairs of subtelocentric chromosomes.
A cytogenetic study of bisexual species belonging to the genera Cirrorhynchus, Dodecastichus and Otiorhynchus is presented in order to confirm their taxonomic position. The karyotype characterization was accomplished by an analysis of mitotic and meiotic chromosomes after differential staining, namely by C-banding, silver impregnation, DAPI and CMA3. A review of the cytogenetic data for the tribe Otiorhynchini contributed to knowledge of chromosomal evolution in this group. An investigation of five of the species studied showed some similarities such as a sex chromosome system of "parachute type" (Xyp), the presence of 10 autosomal bivalents (2n = 22) and heterochromatin localized around centromeres. These observations are similar to those already described for Otiorhynchini species, and confirm the karyological conservatism of this weevil group. In contrast, another species Cirrorhynchus kelecsenyi has an additional four autosomal bivalents (n% = 14 + Xyp, 2n = 30), which differs considerably from the chromosomal homogeneity of the other genera. Karyotypic evolution in this species was achieved most probably by increasing the number of chromosomes by centric fissions, resulting in variation in the number of acrocentric chromosomes. DAPI-positive and CMA3-negative reactions of heterochromatic DNA in all the species studied suggest that it has an AT-rich composition. Impregnating chromosomes with silver nitrate reveals NORs on one pair of autosomes, and probably argentophilic material in the interspace between the X and y sex chromosomes. The karyological findings support the taxonomical revision of Otiorhynchini based on morphological characters.
Heterochromatin is one of the most dynamic components in the genome of species. Previous studies on the heterochromatin content and distribution in Heteroptera (insects with holokinetic chromosomes) have shown that the species belonging to the family Coreidae are interesting model organisms since they show very diverse C bands patterns. In the present work, we analyzed the C-band pattern in individuals of Holhymenia rubiginosa from different populations collected in different years. This species has the diploid karyotype 2n = 27/28 = 24 + 2m + X0/XX (male/female). C-bands are terminally, subterminally or interstitially located on 10-17 chromosomes and a remarkable heterochromatin heteromorphism is observed in the meiotic bivalents: in the presence/absence of bands, in the size of bands and number of bands. A heteromorphism is also inferred in the number of ribosomal genes from the difference in the fluorescent in situ hybridization signals between NOR-homologues. Chiasmata are generally located opposite to conspicuous C-bands, but in some bivalents chiasmata are also observed in close proximity to C-bands. Considering the striking variation in heterochromatin content between individuals and populations it is suggested that heterochromatin should be selectively neutral in H. rubiginosa.
The Coreidae (Heteroptera) have holokinetic chromosomes and during male meiosis the autosomal bivalents segregate reductionally at anaphase I while the sex chromosomes do so equationally. The modal diploid chromosome number of the family is 2n = 21, with a pair of m-chromosomes and an X0/XX sex chromosome system. A 2n = 24/26 (male/female) and an X1X20/X1X1X2X2 sex chromosome system were found in Spartocera batatas (Fabricius). C-banding and fluorescent-banding revealed the presence of AT-rich heterochromatic bands medially located on all the autosomes, and one telomeric band on both the X1 and X2 chromosomes. This banding pattern differed from the telomeric heterochromatin distribution found in most other heteropteran species. The X1 and X2 chromosomes were intimately associated during male meiosis and difficult to recognize as two separate entities. Based on a comparison with the behaviour of sex chromosomes in other coreids and other heteopterans with multiple sex chromosomes it is suggested that the particular behaviour of X1 and X2 chromosomes in coreid species with multiple sex chromosome systems evolved as an alternative mechanism for ensuring the proper segregation of the sex chromosomes during meiosis.
Karyotypes and testis structure of 14 species representing 9 genera (Latissus, Bubastia, Falcidius, Kervillea, Mulsantereum, Mycterodus, Scorlupaster, Scorlupella and Zopherisca) of the planthopper tribe Issini (Issidae) are presented. All the karyotypes are illustrated by meiotic and occasionally mitotic figures. The male karyotypes of most of the species analyzed are 2n = 26 + X, the exception being Falcidius limbatus, which has a karyotype of 2n = 24 + neo-XY. The latter is the first report of the neo-XY system in the family Issidae. The species studied are found to be similar in having NORs on the largest pair of autosomes, but differ significantly in the amount and distribution of C-heterochromatin along the chromosomes. In contrast to the conserved chromosome numbers, the highly variable follicle number in the testes suggests rapid evolution of the tribe Issini. On the basis of its specific follicle number, it is proposed that Zopherisca tendinosa skaloula Gnezdilov & Drosopoulos, 2006 be upgrade to a species: Z. skaloula stat. n. The cytological and taxonomic significance of results presented are discussed.
In this study, the 2n = 58 chromosomal race of blind mole rats,
Nannospalax xanthodon, from the Erzincan province in Turkey was investigated. Conventional chromosome staining, Ag-NOR staining and C-banding analysis were carried out in the specimens studied. The karyotype included three small or medium-sized meta/submetacentric pairs and twenty-five acrocentric pairs of autosomes of gradually diminishing size (NFa = 62). C-heterochromatin regions were found in centromeric and pericentromeric areas or in short arms of some bi-armed autosomal pairs and in pericentromeric areas of a few acrocentric autosomes. The X chromosome had a centromeric C-positive band and the short arm of the Y chromosome appeared to be C-positively stained. The NORs were
localized in distal heterochromatin areas of the short arms of two pairs of biarmed and one pair of acrocentric autosomes. Within the 58 chromosome populations reported from Turkey, two groups can be recognized differing by the presence or absence of a large submetacentric autosomal pair. The populations possessing this marker chromosome occur in central and northern Anatolia, whereas populations form eastern Anatolia have no similar chromosome in their karyotype.