Instability of B-chromosomes in somatic and germline cells of Apodemus peninsulae

Instability of B-chromosomes was estimated in somatic and germline cells of samples Apodemus peninsulae from different localities of the species range. In 84 out of 188 animals (45%), in cells assessed for B-chromosome mosaicism, bone marrow cells with different B-chromosome number were observed. The numbers of B-chromosomes in spermatocytes at the pachytene stage were estimated in ten males. It was shown that the average number of B-chromosomes and the number of cell clones in germline cells was higher than the corresponding numbers in bone marrow cells. The higher number of B-chromosomes and their higher variability in germline cells than in somatic cells suggest the existence of a mechanism of premeiotic accumulation of B-chromosomes in spermatogenesis of A. peninsulae.     

Synaptonemal complexes of the A- and B-chromosomes of the spermatocytes from the East Asian mouse Apodemus peninsulae

The analysis of whole-mount preparations of synaptonemal complexes (SCs) from surface-spread spermatocytes of A. peninsulae (2n = 48A + 1, 2, ... 12 B) had revealed SCs of 23 autosomal bivalents, sex bivalent XY, axial cores and SCs of the B-chromosomes. The intercellular and interindividual variability of the number of B-chromosomes varied from 1 to 12 per cell. The SCs of autosomal bivalents were shown to have a typical structure. The structure and behaviour of SCs of sex bivalent throughout meiotic prophase I appeared to be similar to those observed in other species of this order. Mainly B-univalents and less frequently B-bivalents containing SCs were found to be formed in meiotic prophase I. The full homologues appear to be rarely seen among B-chromosomes of the East-Asiatic mouse. A tendency of forming clusters of B-univalents near the sex bivalent was found, in addition to B-bivalents with lateral elements, having the form of bi- and tri-stranded elements with rare synaptic fragments. Besides this, the SCs of the autosomes of pachytene cells were found to contain structures resembling the recombination nodules.     

Instability of B-chromosomes in somatic and germline cells of Apodemus peninsulae

Instability of B-chromosomes was estimated in somatic and germline cells of samples Apodemus peninsulae from different localities of the species range. In 84 out of 188 animals (45%), in cells assessed for B-chromosome mosaicism, bone marrow cells with different B-chromosome number were observed. The numbers of B-chromosomes in spermatocytes at the pachytene stage were estimated in ten males. It was shown that the average number of B-chromosomes and the number of cell clones in germline cells was higher than the corresponding numbers in bone marrow cells. The higher number of B-chromosomes and their higher variability in germline cells than in somatic cells suggest the existence of a mechanism of premeiotic accumulation of B-chromosomes in spermatogenesis of A. peninsulae     

Variability of the cytogenetic structure of Apodemus peninsula (Rodentia, Muridae) population from the West Sayans region

Karyological investigations of East-Asiatic mice (28 animals) from 5 catching points in the region of West Sayans revealed the presence of 1-12 B-chromosomes in these animals. Nearly all the mice had their individual variant of B-chromosomes system, including combinations of two-shoulder-like chromosomes of different size (from 1 to 5), and also small acrocentric (from 0 to 1) and dot-like B-chromosomes (from 0 to 9). Most frequent were the mice with 5 and 6 (21%) B-chromosomes. The catching points were 120 kilometers from each other, and clinical changes were observed between these points in the direction from the South to the North.     

Evidence of B-chromosomes in the karyotype of Barypeithes pellucidus Boheman 1834 (Coleoptera, Curculionidae, Entiminae) from Central Europe

B-chromosomes were observed in spermatogonial mitotic metaphases, meiotic metaphases I and II of Barpeithes pellucidus from one population in Slovakia. The number of B-chromosomes ranged from one to six per cell and they paired with the sex heterochromosomes in the first meiotic metaphase and rarely with the autosomes. In metaphase I one B-chromosome was always associated with X chromosome forming a tripartite complex. The XyBp was easily recognizable as a complex of three chromosomes in a parachute association The size of the B-chromosomes was approximately the same or a little smaller than that of the y heterochromosome which was the smallest element of the regular chromosome set. Their staining intensity seems to be similar to that of the autosomes and sex chromosomes, respectively. The behaviour of B-chromosomes during mitosis and meiosis in weevils is briefly discussed.     

THE CYTOGENETICS OF XANTHISMA TEXANUM DC. (ASTERACEAE) AND ITS B-CHROMOSOMES

The karyotype of A-set and B-chromosomes of Xanthisma texanum DC. are described in detail and measurements are given. The distribution of B-chromosomes in stem tissue is described and the loss of B-chromosomes from primary roots confirmed. The number of B-chromosomes in pollen mother cells was constant within single inflorescence buds and in all buds throughout the flowering period. The behavior of one and two B-chromosomes during meiosis is described in detail. During meiosis, B₁'s divided in 71% of the cases during anaphase II and in 29% of the cases during anaphase I. First anaphase division resulted in some lagging and elimination of B-chromatids during second division. During anaphase I, B₁₁'s divided into chromosomes and in anaphase II these divided into chromatids in 95% of the cases. In the other 5 % non-disjunction of the B-chromosomes or chromatids and A-set chromosome abnormalities occurred. Post meiotic preferential distribution during pollen mitosis resulting in a doubling of the number of B-chromosomes passed to progeny via pollen occurred, but no doubling occurred in the female line. Crosses involving plants with two B-chromosomes each yielded fewer plants with three B-chromosomes than expected. Polyploidy is extremely rare in the species. The evolutionary significance of B-chromosome behavior is discussed in relation to its origin and survival.     

B-chromosomes in the spermatogenesis of blood-sucking black flies

The karyofund of Odagmia ornata taken from natural population was investigated with the light microscope, the existence of a definite number of specimens with B-chromosomes being discovered. The behaviour of B-chromosomes in the spermatogenesis was analyzed. The dynamics of the number of specimens with B-chromosomes is presumably associated with the peculiarities of their behaviour in meiosis, i.e. with the unequal distribution of these chromosomes in the number of sex cells.     

Nature and role of accessory chromosomes in silver-gray foxes. IV. The behavior of accessory chromosomes in meiosis

Comparison of chromosome number at somatic and spermatogonial mitoses has demonstrated the increase in the number of additional chromosomes in cells of germinal tissue. This may evidence a mechanism of B-chromosomes accumulation in foxes. B-chromosomes may lag as univalents, may form bivalent associations, or occasionally form trivalents at the stage of diakinesis-metaphase I, and they may associate with macrobivalents (A-chromosome bivalents). The analysis of metaphase II has shown that the distribution of B-chromosomes in the second metaphase is random resulting in gametes with various numbers of B-chromosomes.     

Chromosomes in a hybrid zone of Israeli mole rars (Spalax, Rodentia)

Chromosomal novelties and the level of meiotic and mitotic abnormalities were studied in a hybrid zone between two chromosomally differentiated Spalax cytotypes of 2n = 58 and 2n = 52. These cytotypes differ by five Rb fusions, four centromeric shifts accompanied by heterochromatin deletion, one paracentric inversion, and the Y-chromosome reorganization. Among 149 specimens studied, 82 were hybrids with 64 different karyotypes ranging in diploid numbers from 2n = 50 to 2n = 60. Nine hybrid specimens were mosaics for the chromosome numbers due to occurrence of cell lines with different Robertsonian chromosome arrangements, and six specimens possessed variable number of B-chromosomes. Mosaicism of B-chromosomes was found also in meiotic cells however chromatid breaks and abnormal chromosome pairing during meiosis occurred very rarely. All these results imply some local genomic instability resulting in the spontaneous process of reversible Rb fusions.     

Heterochromatic regions in corn A- and B- chromosomes

A collection of maize forms from the Vavilov All-Russia Institute of Plant Breeding (VIR) was studied. We compared variation in the following traits: the number and size of heterochromatic knob regions (HKRs) of chromosomes of mother pollen cells at pachytene depending on the presence (B+) or absence (B0) of B-chromosomes; size of B-chromosomes (general, of heterochromatic part); and the frequency of B+ plants in groups of forms contrasting in the HKR number (10-15, 4-10, 2-7, 1-4). It was shown that B chromosomes had statistically significantly different effects on HKR polymorphism, relative heterochromatin "content" in the cell of multiknob and knobless forms, selection of plants for early ear flowering in these forms. The combination of maximum (and minimum) sizes of heterochromatic regions of A- and B-chromosomes was established; the genomic level of control of the trait is suggested. The role of the relationship of polymorphism at heterochromatic regions of A- and B-chromosomes between them and with the systems of maize reproduction is considered as a mechanism of maintenance of optimum plant heterozygosity via adaptive ontogenetic redistribution of heterochromatin among loci, chromosomes, and gametes.     

Approaches to the analysis of reciprocal chromosome distribution in the bone marrow cells of mice

A study was made of G-banding chromosome preparations made of bone marrow cells of BALB/c mouse females, injected intraperitoneally with a single dose of the antibiotic adriamycin 23 hours before sacrifice. Frequencies of different chromosome fusions in pericentromeric regions were analysed. All chromosomes were found to be involved in the interchromosomal associations, different chromosomes participating in such fusions with different frequency. No associations of homologous chromosomes were observed. For each chromosome a limited number of preferential partners for fusion was revealed, the number of such partners for different chromosomes varying. Almost for a half of chromosomes, chromosome 15 was one of the most preferred partners. Possible significance of the data obtained is discussed for the analysis of principles of the spatial chromosome arrangement in murine bone marrow cells.     

Structure,behaviour and repetitive DNA of B-chromosomes in Cestrum nocturnum (Solanaceae)

Abstract

The Cestrum genus is karyotypically exceptional in Solanaceae. It is characterised by a basic number x?=?8, a large chromosomal and genomic size, complex heterochromatin patterns, B-chromosomes (Bs) with particular heterochromatin and distribution of 18–5.8–26S and 5S rDNA. Cestrum nocturnum L. has a diploid number of 2n?=?16 plus a variable number of B-chromosomes. The aims of work was to analyse their numerical variation, structure and behaviour of C. nocturnum B-chromosomes by classical and molecular cytogenetics. The individuals analysed had 2n?=?16?+?0?13 B-chromosomes. All B-chromosomes were metacentric and smaller than A-chromosomes. The number of B-chromosomes showed a great variability between and within individuals, thereby denoting the occurrence of events that promote mitotic and meiotic instability. Cytogenetic techniques made it possible to observe that B-chromosomes are rich in heterochromatin, probably with AT- and GC-rich regions. In addition, molecular techniques allowed to detect homologous sequences of transposable element conserved domains of Ty1-Copia and Ty3-Gypsy superfamilies. These sequences were located by FISH in all B-chromosomes and some A-chromosomes. Our results showed that repetitive DNA could play an important role in chromosomal evolution as well as in the stability of B-chromosomes in C. nocturnum.     

Chromosomes in a hybrid zone of Israeli mole rars (Spalax, Radentia)

Chromosomal novelties and the level of meiotic and mitotic abnormalities were studied in a hybrid zone between two chromosomally differentiated Spalax cytotypes of 2n = 58 and 2n = 52. These cytotypes differ by five Rb fusions, four centromeric shifts accompanied by heterochromatin deletion, one paracentric inversion, and the Y-chromosome reorganization. Among 149 specimens studied, 82 were hybrids with 64 different karyotypes ranging in diploid numbers from 2n = 50 to 2n = 60. Nine hybrid specimens were mosaics for the chromosome numbers due to occurrence of cell lines with different Robertsonian chromosome arrangements, and six specimens possessed variable number of B-chromosomes. Mosaicism of B-chromosomes was found also in meiotic cells however chromatid breaks and abnormal chromosome pairing during meiosis occurred very rarely. All these results imply some local genomic instability resulting in the spontaneous process of reversible Rb fusions.     

Spontaneous and induced chromosome aberrations in the bone marrow cells of different strains of mice during aging

Sensitivity of bone marrow cell chromosomes to alkylating agent thiophosphamide and to gamma-irradiation has been studied in the course of ageing in 101/H, A/He, CBA, BALB/c and C57BL/6 mice. The effects of both the kinds of mutagenic treatment and of the genotype of the animals on the age-dependent changes in sensitivity of bone marrow cell chromosomes were found. Following gamma-irradiation under our experimental conditions, no variation in the output of chromosomal aberrations was observed between the strains studied. Following thiophosphamide treatment, aged mice of strains 101/H, A/He and CBA showed an increased chromosome instability as compared to young ones. In C57BL/6 mice the level of induced chromosome aberrations was found to be age-independent. Following thiophosphamide treatment, cells with multiple chromosome lesions were found in the bone marrow. The higher instability of aged animals in some strains was mainly due to a sharp increase in the number of such cells. In the intact mice of all the strains studied no age-dependent increase in the number of cells showing structural chromosome aberrations was observed, while accumulation of aneuploid cells varied with genotype.     

Orthovanadate increased the frequency of aneuploid mouse sperm without micronucleus induction in mouse bone marrow erythrocytes at the same dose level

The objective of the current study was to investigate the ability of orthovanadate to induce aneuploidy in mouse sperm and micronuclei in mouse bone marrow cells at the same dose levels. The BrdU-incorporation assay was performed to test if the chemical treatment altered the duration of the meiotic divisions. It was found that orthovanadate (25mg/kg bw) treatment did not cause meiotic delay. To determine the frequencies of hyperhaploid and diploid sperm, male mice were treated by intraperitoneal (i.p.) injection with 5, 15 or 25mg/kg bw orthovanadate and sperm were sampled from the Caudae epididymes 22 days later. Fluorescence in situ hybridization (FISH) was performed with DNA-probes for chromosomes 8, X or Y. Significant increases in the frequencies of total hyperhaploid sperm (p<0.01) were found with 15 and 25mg/kg bw orthovanadate, indicating induced non-disjunction during male meiosis. The dose-response was described best by a linear equation. Orthovanadate did not significantly increase the frequencies of diploid sperm at any of the three doses tested, indicating that no complete meiotic arrest occurred. Orthovanadate was investigated also by the micronucleus test at i.p. doses of 1, 5, 15 or 25mg/kg bw, followed by bone marrow sampling 24h after treatment. None of the orthovanadate doses caused a significant increase in the rates of micronuclei (MN). Since the results show that orthovanadate induced non-disjunction during male meiosis without an accompanying induction of MN in bone marrow erythrocytes under the present experimental conditions and doses, it is concluded that male germ cells (meiosis) are more sensitive to the aneugenic effects of orthovanadate than somatic cells (mitosis). However, induction of micronuclei was reported in the literature with orthovanadate, vanadylsulfate and ammonium metavanadate, which contradicts the notion that vanadium compounds might be unique germ cell aneugens.     

The B-chromosome system of Hypochoeris maculata

Populations of Hypochoeris maculata (Compositae) over a wide area of Europe contain a small proportion of individuals with mitoticallystable B-chromosomes. The telocentric Bs are about one sixth the length of the smallest A-chromosome and are heterochromatic. Offspring grown from seeds of natural populations have one or at most two B-chromosomes although plants with up to five Bs have been produced in experiment. The Bs rarely pair during meiotic prophase and the univalents usually undergo centric division at anaphase I. Despite lagging, the Bs are rarely lost during male meiosis. The inheritance of the B-chromosomes differs between the two sides with accumulation in the egg and random inheritance or loss on the pollen side. Although meiotic drive may play some part in the maintenance of the B-polymorphism there is a strict upper limit on the number of Bs in natural populations.     

B-chromosome systems in the pocket mouse,Perognathus baileyi: Meiosis and C-band studies

The heterochromatin characteristics and meiotic behavior of the B-chromosome system of the pocket mouse, Perognathus baileyi, are described. B-chromosomes are associated both with a meiotic accumulation mechanism and with an increase in average chiasma frequency in the A-chromosome set in males. Three morphological classes of B-chromosomes are recognizable, and the mechanisms of origin of each are discussed.     

加拿大一枝黄花的核型分析及B染色体初报

对安徽蚌埠地区外来植物加拿大一枝黄花的染色体核型进行了分析。结果如下:该入侵种的染色体数为2n=50,各染色体间形态差异不明显,均为中着丝粒或近中着丝粒染色体,最长与最短染色体相对长度比为1.72,全套染色体未见随体,核型公式为2 n=50=38 m 12 sm 6 B s,核型类型为较对称的2A型。首次报道了存在于体细胞中的异于常染色体的6个B染色体,这些B染色体在不同细胞中保持恒定的数目,并讨论了B染色体的存在与加拿大一枝黄花在新生境中具有入侵性之间的关系。     

Genetic control of synapsis and recombination in Lolium amphidiploids

Homologous bivalent formation in amphidiploids of Lolium is promoted during meiosis by diploidising genes carried by A-chromosomes and by supernumerary B-chromosomes. The site and mode of action of these diploidising factors were investigated by comparing the relative frequencies of pairing configurations at meiotic prophase and metaphase I in several different hybrid genotypes. The results indicate that diploidising genes act predominatly by increasing the stringency of synapsis at early stages of meiotic prophase. By contrast, B-chromosomes appear to promote bivalent formation by ensuring that homoeologously paired chromosome segments within multivalents do not crossover. The results show that the additive effects of diploidising genes and B-chromosomes are to a certain extent separable in terms of their mode of action and timing during meiosis.     

丽纹攀蜥粗线期染色体核型及微小染色体的分析

本文以精巢、四肢骨和脊椎骨为材料,利用直接制片法制备了丽纹攀蜥（Japalura splendida）染色体标本,首次对其精巢减数分裂粗线期染色体,特别是微小染色体的长度进行了测量,描述了染色体特征,并进行了核型分析.同时与二倍体细胞染色体的核型进行了比较,发现11对微小染色体类型中包括8对中着丝粒染色体、2对端着丝粒染色体和1对点状染色体.