Low Chromosome Number Research Articles

Characterization of chromosome structures of Falconinae (Falconidae, Falconiformes, Aves) by chromosome painting and delineation of chromosome rearrangements during their differentiation

Karyotypes of most bird species are characterized by around 2n = 80 chromosomes, comprising 7-10 pairs of large- and medium-sized macrochromosomes including sex chromosomes and numerous morphologically indistinguishable microchromosomes. The Falconinae of the Falconiformes has a different karyotype from the typical avian karyotype in low chromosome numbers, little size difference between macrochromosomes and a smaller number of microchromosomes. To characterize chromosome structures of Falconinae and to delineate the chromosome rearrangements that occurred in this subfamily, we conducted comparative chromosome painting with chicken chromosomes 1-9 and Z probes and microchromosome-specific probes, and chromosome mapping of the 18S-28S rRNA genes and telomeric (TTAGGG)( n ) sequences for common kestrel (Falco tinnunculus) (2n = 52), peregrine falcon (Falco peregrinus) (2n = 50) and merlin (Falco columbarius) (2n = 40). F. tinnunculus had the highest number of chromosomes and was considered to retain the ancestral karyotype of Falconinae; one and six centric fusions might have occurred in macrochromosomes of F. peregrinus and F. columbarius, respectively. Tandem fusions of microchromosomes to macrochromosomes and between microchromosomes were also frequently observed, and chromosomal locations of the rRNA genes ranged from two to seven pairs of chromosomes. These karyotypic features of Falconinae were relatively different from those of Accipitridae, indicating that the drastic chromosome rearrangements occurred independently in the lineages of Accipitridae and Falconinae.

The litter size in chromosomally polymorphic blue foxes.

Makinen, A. and Lohi, O. 1987. The litter size in chromosomally polymorphic blue foxes. —Hereditas 107:115–119. Lund, Sweden. ISSN 0018–0661. Received December 10, 1986 About 50 % of the Finnish farm bred blue foxes have a Robertsonian translocation in a heterozygous form, whereas the distributions of the homozygous form 2n = 48 and the 2 n = 50 karyotype with two acrocentric autosome pairs seem to be nearly equal. The effect on fertility exerted by the heterozygous Robertsonian translocation was studied on the material from a blue fox farm in Finland during four years. It is concluded that there is a tendency to litter size reduction in mating groups 2n = 49 compared to the 2n = 48 and 2n = 50 mating groups. In this investigation, the 2n = 48 chromosome constitution in parental blue fox groups has every year had a slight tendency to increase the litter size. In addition, the segregation of the karyotypes within the litters of the parental 2n = 49 mating groups is in favour of the 2n = 48 karyotype. Hence, an evolutional tendency towards lower chromosome number without any acrocentric autosomes seems to be indicated.

Evolution in Carex L. sect. Spirostachyae (Cyperaceae): A molecular and cytogenetic approach

Carex sect. Spirostachyae comprises 25 species displaying the centre of diversity in Eurasia. Phylogenetic analysis of the ITS nrDNA region of 20 species of sect. Spirostachyae, six species of sect. Ceratocystis, five species of sect. Elatae, and eight outgroup species reveals that neither sect. Spirostachyae nor sect. Elatae is monophyletic. With the exclusion of Carex cretica, the 19 species of sect. Spirostachyae studied form a clade with the five species of tropical-subtropical sect. Elatae. Taxonomy of the core Spirostachyae is not only mostly in agreement with our phylogenetic hypothesis, but also with ecological and new cytogenetic results. Two main groups with different chromosome numbers and edaphic preferences are identified in the core Spirostachyae. One includes primarily acidophilous species with high chromosome numbers (2 n=(64)68–84), whereas the other one includes mainly basophilous species with lower chromosome numbers (2 n=60–74(75)). Chromosome-number variation is extremely different in the core Spirostachyae, showing great stability in some widespread species (e.g. Carex extensa) but an active chromosome evolution – faster chromosomal rearrangements, fusion and fission events than ITS nucleotide substitutions – in more restricted species (e.g. Carex troodi). Biogeography of the two amphiatlantic pairs of species reveals two independent colonizations of South America from the European continent. The geographical barrier of the Strait of Gibraltar has played different roles in the course of evolution of this section, acting as an effective barrier to gene flow in one case ( Carex helodes) but as a limited barrier or recent separation in two others ( Carex distans, Carex punctata).

The first karyotype study in palpigrades, a primitive order of arachnids (Arachnida: Palpigradi)

Chromosomes of palpigrades (Arachnida: Palpigradi), a rare arachnid order with numerous primitive characters, were studied for the first time. We analysed two species of the genus Eukoenenia, namely E. spelaea and E. mirabilis. Their karyotypes are uniform, consisting of a low number of tiny chromosomes that decrease gradually in size. Study of the palpigrade karyotype did not reveal morphologically differentiated sex chromosomes. Analysis of E. spelaea showed that constitutive heterochromatin is scarce, GC-rich, and restricted mostly to presumed centromeric regions. Meiosis is remarkable for the presence of a short diffuse stage and prominent nucleolar activity. During prophase I, nuclei contain a large nucleolus. Prominent knob at the end of one bivalent formed by constitutive heterochromatin is associated to the nucleolus by an adjacent NOR. Presence of a nucleolus-like body at male prophase II suggests activity of NOR also during beginning of the second meiotic division. The data suggest acrocentric morphology of palpigrade chromosomes. Palpigrades do not display holocentric chromosomes which appear to be apomorphic features of a number of arachnid groups. These are: acariform mites, buthid scorpions, and spiders of the superfamily Dysderoidea. Therefore, cytogenetic data do not support a close relationship of palpigrades and acariform mites as suggested previously.

Direction of karyotype evolution in the bug family Nabidae (Heteroptera): New evidence from 18S rDNA analysis

The bug family Nabidae (Heteroptera) includes taxa showing either a low chromosome number 2n = 16 + XY or high chromosome numbers 2n = 26 or 32 + XY. In order to reveal the direction of karyotype evolution in the family, a molecular phy- logeny of the family was created to reveal the taxon closest to the ancestral type and hence the ancestral karyotype. The phylogeny was based on a partial sequence of the 18S rDNA gene of both high and low chromosome number species belonging to the subfami- lies Prostemmatinae and Nabinae. Phylogeny created by the Neighbour Joining method separated the subfamilies, Prostemmatinae and Nabinae, which form sister groups at the base of this phylogenetic tree, as well as within the Nabinae, tribes Nabini and Arach- nocorini. Combining karyosystematic data with the phylogeny of the family indicated that the ancestral karyotype was a high chro- mosome number, consisting of 2n = 32 + XY. During the course of evolution changes have occurred both in meiotic behaviour of the sex chromosomes and in the number of autosomes. The direction of karyotype evolution was from a high to low autosome number. Abrupt decreases in the number of autosomes have occurred twice; firstly when the tribe Arachnocorini differentiated from the main stem in the subfamily Nabinae and secondly within the tribe Nabini, when within the genus Nabis 2n = 16 + XY species diverged from the 2n = 32 + XY species. A scheme of the sequence of events in karyotype evolution during the evolution of the Nabidae is presented.

Intra- and intergenomic homology of B-genome chromosomes in trigenomic combinations of the cultivated Brassica species revealed by GISH analysis

Intragenomic chromosome homology in the B genome of Brassica nigra and their homoeology with the chromosomes of the A-genome of B. rapa and C-genome of B. oleracea was investigated in triploids (ABC, n = 27) of different origins obtained following hybridizations between natural B. napus (AACC, 2n = 38) x B. nigra (BB, 2n = 16) [AC.B], synthetic B. napus x B. nigra [A.C.B] and B. carinata (BBCC, 2n = 34) x B. rapa (AA, 2n = 20) [BC.A]. A relatively high percentage of pollen mother cells (PMCs) with at least one B-genome chromosome paired allosyndetically with A/C chromosomes was evident in all three combinations. A maximum of three B-genome chromosomes undergoing allosyndesis per cell was observed in AC.B and A.C.B combinations. A maximum of two autosyndetic bivalents within the B genome appeared at diakinesis in all combinations. The accurate analyses of auto- and allo-syndetic pairing for B genome in trigenomic combinations provided further evidence for the hypothesis that the three basic diploid genomes of the cultivated Brassica species evolved from one common ancestral genome with a lower chromosome number. The results showed that Brassica diploids may not be ancient polyploids but may have undergone chromosomal duplications instead of whole-genome duplication. The relevance of these results along with genetic changes of progenitor genomes which occurred during the evolution of Brassica polyploids is discussed.

Karyotype characterization and ZZ/ZW sex chromosome heteromorphism in two species of the catfish genus Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from the Amazon basin

We present karyotypic characteristics and report on the occurrence of ZZ/ZW sex chromosomes in Ancistrus ranunculus (rio Xingu) and Ancistrus sp. "Piagaçu" (rio Purus), of the Brazilian Amazon. Ancistrus ranunculus has a modal number of 2n=48 chromosomes, a fundamental number (FN) of 82 for both sexes, and the karyotypic formula was 20m+8sm+6st+14a for males and 19m+9sm+6st+14a for females. Ancistrus sp. "Piagaçu" presented 2n=52 chromosomes, FN= 78 for males and FN= 79 for females. The karyotypic formula was 16m+8sm+2st+26a for males and 16m+9sm+2st+25a for females. The high number of acrocentric chromosomes in karyotype of Ancistrus sp. "Piagaçu" differs from the majority of Ancistrini genera studied so far, and may have resulted from pericentric inversions and translocations. The lower number of chromosomes in A. ranunculus indicates that centric fusions also occurred in the evolution of Ancistrus karyotypes. We conclude that karyotypic characteristics and the presence of sex chromosomes can constitute important cytotaxonomic markers to identify cryptic species of Ancistrus. However, sex chromosomes apparently arose independently within the genus and thus do not constitute a reliable character to analyze phylogenetic relations among Ancistrus species.

Karyotypic variability in rat kangaroo cell lines cultivated on fibronectin-coated surface

Numerical and structural karyotypic variability was investigated in the NBL-3-17 and NBL-3-11 “markerless” rat kangaroo kidney cell lines cultivated on a fibronectin-coated surface. For the NBL-3-17 cell line grown on a fibronectin-coated surface for periods of 1, 2, 4 and 8 days, the chromosome number distribution changed. These changes involved a significant decrease in the frequency of cells with the modal chromosome number and an increase in the frequency of cells with a lower chromosome number. Many new additional structural variants of the karyotype (SVK) appeared. The observed alterations seem to be due to the predominant adhesion of cells with a lower chromosome number, disturbances of the mitotic apparatus and selection for SVK adapted to the changes in culture conditions. Detachment of cells from the fibronectin-coated surface followed by 5 days cultivation on a hydrophilic surface restored the control cell distribution. For the NBL-3-11 cell line cultured on the fibronectin-coated surface for 1, 2, 4 and 8 days, the numerical karyotypic variability did not change compared to control variants. For the NBL-3-17 cell line grown on a fibronectin-coated surface for 1, 2, 4 and 8 days, the frequency of chromosomal aberrations also did not change relatively to the control. In the NBL-3-11 cell line, the frequency of chromosomal aberrations under the same conditions significantly increased, mainly due to chromosome and chromatid breaks and dicentrics (telomeric associations). The differences in the numerical and structural karyotypic variability between NBL-3-17 (hypotriploid) and NBL-3-11 (hypodiploid) cell lines cultivated on fibronectin are discussed. It is assumed that the observed differences in the karyotypic variability between these cell lines were determined by the specific karyotypic structure of the NBL-3-11 cell line and the altered gene expression of the NBL-3-17 hypotriploid cell line caused by increased doses of certain functioning genes.

Karyomorphological Studies of Four Species of Japanese Scleria (Cyperaceae)

Four species of Japanese Scleria were used for karyomorphological studies. Chromosome numbers of S. mikawana (2n=20) and S. levis (2n=48) were determined for the first time. Our finding of 2n=30 for S. parvula and 2n=48 for S. terrestris differs from those of previous studies. Two major groups were identified in the genus Scleria by karyomorphological data: (1) low chromosome numbers and x=5, (2) high chromosome numbers (2n=48). These karyomorphological data support the taxonomical treatment of 2 sections by Ohwi (1944). The high chromosome numbers may arise by polyploidy of low chromosome numbers because chromosome sizes were almost equal in both. Therefore, chromosomal evolution in the genus Scleria may be caused by polyploidy, rather than aneuploidy.

Development of Bovine Nuclear Transfer Embryos Using Life-span Extended Donor Cells Transfected with Foreign Gene

This study was performed to determine the developmental potentials of nuclear transfer (NT) embryos using life-span extended cells transfected with a foreign gene as donor cells. A life-span extended bovine embryonic fibroblast cell line was transfected with an expression vector in which the human type II collagen (BOMAR) and ear fibroblasts were used as a donor cell. Cytogenetic analysis was performed to analyze the chromosomal abnormality of donor cells. The fusion rate of 1.8 kV/cm for given twice was significantly higher than that of other groups (p given once compared to other groups (p40 passages) had a lower number of chromosomes; however, fresh granulosa cell (GC) and BOMAR groups cultured less than 20 passages had normal chromosome numbers. Both >40 passages BOMAR groups had numerous obscure debris in metaphase spreads. The transfected foreign gene was expressed in all BOMAR groups, but not in the GC group. Based on these results, the lower developmental potential of NT embryos using life-span extended donor cells transfected with a foreign gene might be a cause of chromosomal abnormality in donor cells.

Chromosome counts in the genusAlchemilla (Rosaceae) from SW Europe

This paper presents the results of a karyological analysis of 14 species ofAlchemilla L. collected from SW Europe (Spain and French Pyrenees). About 75% of the analyzed species have chromosome numbers 2n = 95–136. A few species have lower chromosome numbers. The chromosome numbers of 13 species are presented for the first time.

Molecular Phylogeny of Cryptocercus Wood-roaches Based on Mitochondrial COII and 16S Sequences, and Chromosome Numbers in Palearctic Representatives

Woodroaches of the genus Cryptocercus are subsocial and xylophagous cockroaches, distributed in North America and Asia. Studies on male chromosome number in Nearctic species have shown that diploid numbers vary from 2n=37 to 2n=47; numbers from Palearctic species were heretofore unknown. Two hypotheses have been proposed to explain the varying number of chromosomes among Nearctic species: the serial reduction hypothesis, and the parallel scenario. We performed phylogenetic analyses of the COII gene in these species and found evidence for the topology (47(45(43(39,37), which is congruent with the serial reduction hypothesis. We also determined chromosome numbers for the first time in Palearctic species, and found Cryptocercus primarius and Cryptocercus relictus to have relatively low chromosome numbers (2n=17-21) compared to their Nearctic relatives. Finally, our study determined the phylogenetic position of Cryptocercus primarius among other Asian taxa.

Karyotype characterization of Trigona fulviventris Guérin, 1835 (Hymenoptera, Meliponini) by C banding and fluorochrome staining: report of a new chromosome number in the genus

Although many species of the genus Trigona have been taxonomically described, cytogenetic studies of these species are still rare. The aim of the present study was to obtain cytogenetic data by conventional staining, C banding and fluorochrome staining for the karyotype characterization of the species Trigona fulviventris. Cytogenetic analysis revealed that this species possesses a diploid chromosome number of 2n = 32, different from most other species of this genus studied so far. This variation was probably due to the centric fusion in a higher numbered ancestral karyotype, this fusion producing the large metacentric chromosome pair and the lower chromosome number observed in Trigona fulviventris. Heterochromatin was detected in the pericentromeric region of the first chromosome pair and in one of the arms of the remaining pairs. Base-specific fluorochrome staining with 4'-6-diamidino-2-phenylindole (DAPI) showed that the heterochromatin was rich in AT base pairs (DAPI+) except for pair 13, which was chromomycin A3 (CMA3) positive indicating an excess of GC base pairs. Our data also suggests that there was variation in heterochromatin base composition.

Plantago ovata: genetic diversity, cultivation, utilization and chemistry

Plantago ovatais the cultivated and economically important species in the monotypic genusPlantago. P. ovatais a short-stemmed annual herb, 10–45 cm tall. The species is generally an in-breeder. The seed husk of this plant is commonly called Psyllium or Isabgol (in Hindi), which is a very effective laxative. Other usages of Isabgol are in ice cream making, cosmetics, printing and finishing. The intake of husk also reduces blood cholesterol levels. Isabgol is commercially very important as its export earns India foreign exchange worth INR 2.5 billion (US$1=44 INR). The plant is cultivated on a large scale in western India. In Gujarat, it is cultivated in about 144,000 ha of land, yielding 720 kg/ha.P. ovatahas a narrow genetic base, and the lack of variability is on account of low chromosome number, small chromosome size, presence of high heterochromatin in the chromosomes, low chiasmata frequency and low recombination index. The genome size of the species is ∼500 Mb. Different breeding methods, namely selection, hybridization, induced mutations, polyploidy and tissue culture, have been used for genetic improvement of this plant. Except selections, which have led to isolation of a few varieties, the results of other methods have not been encouraging.P. ovatahas about 200 wild allies, some of which are medicinally important. These wild species constitute a rich resource of important genes, which if transferred to cultivated species could revolutionize the production of Isabgol. The present paper highlights various aspects of genetic diversity, cultivation and utilization of this important medicinal plant, and suggests the prospects of genetic manipulation.

Molecular cytogenetic characterization of parental genomes in the partial amphidiploid Triticum aestivum x Thinopyrum ponticum

The wheat line PF 839197 and six hybrid derivatives from a cross between PF 839197 and Thinopyrum ponticum were cytologically characterized by fluorescent in situ hybridization (FISH). Probes for the 5S and 45S rDNA genes (pTa794 and pTa71, respectively), a highly repetitive rye sequence (pSc119.2), the synthetic oligonucleotide (AAG)5, and total genomic DNA from Th. ponticum and rye were used. In the wheat line, a 1RS.1BL translocation was revealed by the labeling patterns produced with pSc119.2 and (AAG)5, and confirmed by genomic in situ hybridization (GISH) using rye genomic DNA as a probe. Analyses of partial amphiploids confirmed previous results indicating mitotic instability, with a tendency to stabilize at 2n = 42 or 56. GISH with Th. ponticum genomic DNA showed that in one hybrid derivative, with lower chromosome numbers (2n = 42-45), chromosomes were not labeled, whereas in the hybrids with 2n = 48-56 up to 14 chromosomes were labeled. These data suggest that the original chromosome set of these hybrids was 2n = 56, and that chromosomes from both genomes were lost by mitotic instability. FISH using the rDNA probes and GISH with Thinopyrum genomic DNA suggested that cells with 2n = 56 contained an entire wheat genome plus two monoploid chromosome sets of Th. ponticum.

Life history evolution and genome size in subtribe Oncidiinae (Orchidaceae).

Within Oncidiinae, there are several groups of species that are effectively annuals, and we wished to see if these species had smaller genome sizes than average for the subtribe. Fifty-four genome size estimates (50 of which are new) for species in subtribe Oncidiinae (Orchidaceae) were examined for the first time in a phylogenetic context to evaluate hypotheses concerning genome sizes and life history traits. Within the limits of still relatively sparse sampling, the species that are effectively annuals do appear to have smaller genome sizes than average. However, the genome sizes of their immediate sister group are also small, indicating that changes in genome size preceded the change in life history traits. Genome sizes and chromosome numbers also do not correlate; some slowly growing species have lower chromosome numbers but large genomes and vice versa. Based on a survey of the literature on orchids, it is also clear that epiphytic species have smaller genome sizes than do terrestrial species, which could be an effect of different water relations or the fact that most terrestrial orchids are geophytic or have distinct growth and dormancy phases.

Low chromosome number angiosperms

Plant with very low chromosome number are of interest for the analysis of the structure of chromosome and chromatin organization. Many studies have been carried out on the evolution of the karyotyp...

Cytogenetic analysis of Ctenostomini by C-banding and rDNA localization and its relevance to the knowledge of the evolution of tiger beetles (Coleoptera: Cicindelidae)

In this work, the first cytogenetic data on Neotropical Collyrinae is provided, by way of their karyotypes, C-banding and ribosomal genes (rDNA) localization using fluorescence in situ hybridization (FISH). The two species analysed, Ctenostoma (Procephalus) ornatum ornatum (male) and Ctenostoma (Euctenostoma) rugosum (female) showed, respectively, a diploid number of 17 and 18 chromosomes. C. ornatum ornatum has a multiple sex chromosome system (n = 7 + X1X2Y), and mitotic and meiotic metaphase cells showed rDNA gene labelling in the smallest autosomal pair. In this species, no C-bands were obtained, while C. rugosum seems to exhibit centromeric and/or interstitial C-bands in almost all chromosomes. The observation of a multiple sex chromosome system in Ctenostomini ensured the appearance of this characteristic in the hypothetical ancestral of Collyrinae and Cicindelini. The subfamily Collyrinae is not uniform in what concerns diploid chromosome number and rDNA gene localization, because C. ornatum ornatum possesses a lower chromosome number and autosomal rDNA genes when compared with the other Collyrinae species studied (Neocollyris spp.). Independent events leading to the reduction in chromosome number might have taken place during the split of the Collyrinae into the tribes Ctenostomini and Collyrini.

Effect of interferon-α on chromosome abnormalities in treated chronic myelogenous leukemia patients

To investigate the relationship of chromosomal aberrations at blastic crisis (BC) in chronic myelogenous leukemia (CML), with previous therapies and with atomic bomb (AB) exposure, we studied 114 CML patients who developed BC, including 23 AB survivors in Hiroshima. In total, only 45.6% showed major-route abnormalities, which figure was far lower than those previously reported, implying possibility of geographical difference. Occurrence of major-route abnormality was not associated with either duration of chronic phase or survival time after BC. Patients treated with interferon-alpha (IFNalpha) showed lower frequency of major-route abnormalities and lower number of abnormal chromosomes than did patients treated with busulfan (Bu). The frequency of trisomy 8 was lower and monosomy 7 was higher in IFNalpha-treated than in Bu-treated patients. The frequency of unusual abnormalities at BC in IFNalpha-treated patients was indistinguishable from those in Bu-treated patients and, notably, a more common (40%) feature in IFNalpha-treated patients was no change in the cytogenetic picture. Thus, we conclude that IFNalpha action on chromosome aberration is basically quite neutral and that IFNalpha does not induce any specific aberrations, including unusual ones at BC, with an exception of deletion of chromosome 7. Atomic bomb exposure status did not make any difference in secondary abnormalities at BC.

Resistance to barley yellow dwarf virus, powdery mildew and leaf rust in wheat x Thinopyrum backcrosses

Wheat (Triticumaestivum) relatives are sources of useful genes for disease resistance. Chromosomally segregating populations of intergeneric hybrids between wheat and its distantly related species provide opportunity to study and introgress multiple disease resistance. While introgressing resistance to barley yellow dwarf virus (BYDV) from Thinopyrum into wheat, which is susceptible to BYDV, we scored powdery mildew (Erysiphaegraminis) and leaf rust (Pucciniatriticina) resistance, and chromosome numbers in second and third backcrosses (BC2 and BC3) of intergeneric hybrids of wheat with Thinopyrum ponticum and Thinopyrumintermedium. The frequency of multiple resistance to all the three diseases was low or became low when selection was applied for BYDV resistance and low chromosome numbers. Selection for fewer alien chromosomes while maintaining BYDV resistance was more effective in wheat x T. intermedium than in the wheat x T. ponticum cross. Mean chromosome numbers were significantly different in BC3 generation between BYDV resistant and susceptible plants in both crosses. Significant negative correlations between chromosome numbers and enzyme-linked immunosorbent assay (ELISA) values showed that as the critical Thinopyrum chromosome(s) were eliminated, susceptibility to BYDV increased. Results indicated that it is unlikely that genes for full resistance to all three diseases can be transferred simultaneously from Thinopyrum to wheat.