Contributions to the Cytotaxonomy of the Commelinaceae. Gibasis linearis and its allies

Species of the Gibasis linearis alliance collected in Mexico in 1976 are shown to have a chromosome constitution of x = 6, but x = 5 has also been found in some populations of G. rhodantha and G. speciosa. These two basic numbers are associated with distinctive karyotypes, 2M + 4A and 3M + 2A respectively, which show a Robertsonian relationship with each other. The existence of 2n = 22 in G. speciosa , combining both basic numbers at the amphidiploid level provides evidence of pairing between metacentrics and acrocentrics in such a way as to substantiate the view that fusion or fission of chromosomes is responsible for the modification of basic number. This survey provides a basis for other studies which will determine the chromosome relationships of the species irrespective of chromosome number in this family.     

Contributions to the Cytotaxonomy of the Commelinaceae. Gibasis linearis and its allies

Species of the Gibasis linearis alliance collected in Mexico in 1976 are shown to have a chromosome constitution of x = 6, but x = 5 has also been found in some populations of G. rhodantha and G. speciosa. These two basic numbers are associated with distinctive karyotypes, 2M + 4A and 3M + 2A respectively, which show a Robertsonian relationship with each other. The existence of 2n = 22 in G. speciosa , combining both basic numbers at the amphidiploid level provides evidence of pairing between metacentrics and acrocentrics in such a way as to substantiate the view that fusion or fission of chromosomes is responsible for the modification of basic number. This survey provides a basis for other studies which will determine the chromosome relationships of the species irrespective of chromosome number in this family.     

Mauritius type black rats with peculiar karyotypes derived from robertsonian fission of small metacentrics

All seventeen black rats collected from Mauritius Island were characterized by having many extra small acrocentric autosomes. Their basic karyotype was of Oceanian type, because of the presence of the large metacentric M₁ and M₂ pairs, but chromosome numbers in 13 specimens among them were 42, those of 3 specimens 43, and those of the remaining one specimen 44. Although the Oceanian type rat had 2 small acrocentric autosomes (pair no. 13), 16 Mauritius rats had 10 small acrocentrics, and the remaining one had 8 small acrocentrics. Comparative karyotype analysis between Oceanian and Mauritius type rats showed that the extra small acrocentrics found in Mauritius rats were due to Robertsonian fission of small metacentric pairs no. 14 and 18 of the original Oceanian type rat. Only one rat with 8 small acrocentrics showed the heteromorphic pair no. 18 consisting of one metacentric and two acrocentrics. The large metacentric M₁ chromosome in 13 of 17 rats examined showed homologous pair, but two of them were heteromorphic by involving one metacentric M₁ and two acrocentrics. In the remaining two rats M₁ chromosome was not observed, but acrocentric pairs no. 4 and 7 were included. These acrocentrics were also suggested to be originated from Robertsonian fission of the large metacentric M₁ chromosome. Robertsonian fission seemed to be one of the important mechanism found in karyotype evolution.     

The karyology of the Common shrew, Sorex araneus Linné, 1758 (Insectivora, Soricidae) in southwestern Germany

Presented is the karyotype of Sorex araneus from 4 trapping sites in southwestern Germany. From this species nearly 20 chromosomal races have so far been described. In the study area autosomal numbers of 2n_a= 22–24 were recorded. The characteristical metacentrics jl, hi, gm, kr and the acrocentrics n, o, p, q were identified by G-banding. The element kr shows Robertsonian polymorphism. The metacentrics only allow a classification of the studied populations as chromosomal race “Vaud” from Switzerland. The postglacial recolonization and the possible presence of other chromosomal races in the central and northern parts of Germany are briefly discussed. Different selection pressures act on metacentrics and acrocentrics in central populations of a chromosomal race in contrast to those living in contact zones of different chromosomal races. It is suggested that the smaller autosomal arms are subject to weaker selection pressure to be fixed as metacentrics.     

The role of chromosome rearrangements in the evolution of mole voles of the genus Ellobius (Rodentia,Mammalia)

Modern mole voles of the genus Ellobius are characterized by species-specific features of autosomes and sex chromosomes. Owing to the use of the Zoo-FISH method, the nomenclature of chromosomes was refined and nonhomologous Robertsonian translocations indistinguishable by G-staining were identified for Ellobius tancrei, which is a species with a wide chromosome variation of the Robertsonian type. The electron-microscopic analysis of synaptonemal complexes in F₁ hybrids of forms with 2n = 50 and 2n = 48 revealed the formation of a closed SC-pentavalent composed of three metacentrics with monobrachial homology and two acrocentrics. Segregation of chromosomes of such complex systems is impeded by disturbances in the nucleus architecture leading to the formation of unbalanced gametes and to a dramatic reduction in fertility of hybrids. Our data support the hypothesis that the formation of monobrachial homologous metacentric chromosomes can be considered as a way of chromosomal speciation.     

Synaptonemal complex analysis of heteromorphic trivalents in Lemur hybrids

Synaptonemal complexes (SCs) in surface spread pachytene spermatocytes of Lemur resemble those in other mammals and are of two types: metacentric (or submetacentric) and acrocentric, with a very short second arm. In autosomal SC and mitotic karyotypes of Lemur fulvus (2n=60) a 11 proportionality in relative length is observed as in other mammals. In an intraspecific lemur hybrid (2n=55) obtained by mating L. fulvus rufus (2n=60) x L. fulvus collaris (2n=51), G-band patterns show that 10 single acrocentric mitotic chromosomes correspond to the arms of 5 single metacentrics, implying homology. It is inferred that the metacentrics have evolved by centric (Robertsonian) fusion of the acrocentrics. In the SC karyotype of the hybrid all SCs are normal except for five which have the configurations expected of metacentric-acrocentric trivalents. Similarly, in L. f. collaris (2n= 51), with one unpaired metacentric and two unpaired acrocentrics, one such SC trivalent is present in the complement. In an SC trivalent, each of the acrocentric long axes is synapsed with an arm of the metacentric axis, confirming the homology predicted from banding similarities. At late zygotene, the acrocentric short arms, which are non-homologous, are the last to pair, demonstrating that synapsis of the homologous arms occurs first. At later pachytene the acrocentric short arms are fully synapsed, producing a short SC side arm. This subsequent non-homologous synapsis is taken to be an instance of the synaptic adjustment phenomenon which has been shown to lead to non-homologous synapsis in a duplication and several inversions in the mouse. The kinetochore of the metacentric is the same size as those of the acrocentrics, and thus is unlikely to have arisen by true centromeric fusion, but rather by a translocation. The kinetochores of the acrocentrics always lie together on the same side of the metacentric kinetochore (cis configuration), implying a single pairing face on the metacentric axis. The observed trivalent configuration may well constitute a prerequisite for proper meiotic disjunction in metacentric-acrocentric heterozygotes. Such a mechanism is consistent with fertility regularly observed in such hybrid lemurs.     

Chromosomes of the caryophyllidean tapeworm Glaridacris laruei

The chromosomes of the monozoic tapeworm Glaridacris laruei, from 4 locations in New York State, were studied in leucobasic fuchsin stained squashes of testes and vitelline cells. The diploid chromosome number is 16. Metaphase figures from vitelline cells consist of 3 pairs of metacentrics (“V's”), 4 pairs of acrocentrics (“rods”), and 1 pair of submetacentrics (“J's”). The complement is characterized by a pair of metacentrics 9 μm long, representing 11.5% of the total chromosome length. The shortest are acrocentrics, 2–4 μm long. Meiosis was observed only in spermatogenesis, which proceeds as usual with normal sperm formed after 2 meiotic divisions. Colchicine pretreatment did not facilitate analysis of chromosomes. The scarcity of cell division in 2 populations of G. laruei suggests a possible mitotic rhythm or temperature effect on cell division. Similarities were observed between the the complements of G. laruei and Hunterella nodulosa (2n = 14). A theoretical idiogram, constructed from that of G. laruei, closely resembles H. nodulosa, indicating that there may be a close cytological relationship between these phenotypically different caryophyllids. An idiogram and photographs of chromosomes supplement the paper.     

Banding pattern analysis of polymorphic karyotypes in the black rat by a new differential staining technique

Polymorphic karyotypes of black rats (Rattus rattus) collected in Japan, Australia and India were analysed by a new differential staining technique by which banding patterns in the metaphase chromosomes are revealed. The technique consists in two steps: immersion of slides in a mixture of 2 x SSC and 0.1% (w/v) SDS (sodium dodecyl sulfate) for a few seconds at room temperature, and staining in Giemsa. By this treatment characteristic banding patterns were obtained in each chromosome pair. From the banding pattern analysis, subtelocentric pairs No. 1 and 9, which are polymorphic in respect to the acrocentrics and the subtelocentrics, were proven to have originated by pericentric inversion in the acrocentrics. The origin of two large metacentrics observed in Australian and Indian black rats was confirmed to have been developed by Robertsonian fusion of the acrocentrics No. 4 and 7 and No. 11 and 12 present in the Asian type black rat.Contribution No. 873 from the National Institute of Genetics, Japan. Supported by a grant-in-aid from the Ministry of Education of Japan (Nos. 92159 and 92332).     

Cytogenetic control of a hybrid zone between two <Emphasis Type="Italic">Sorex araneus</Emphasis> chromosome races before breeding season

Two chromosome races of common shrew, Moscow and Seliger, differ in the arm combination in 11 diagnostic chromosomes (Robertsonian metacentrics/acrocentrics). Homozygotes of both pure races, simple Robertsonian heterozygotes of Seliger race, and complex heterozygotes (F₁ hybrids) were detected in the found earlier hybrid zone of these races, in the spring before the breeding season. The g/o heterozygote was first discovered in race Seliger, whose chromosome formula typically contains acrocentrics g and o. The m/q heterozygote was recorded for the second time. Meiosis was studied in 16 males representing five detected karyotypic categories. No abnormal in pairing of homologs in either sex trivalent common for the species (XY1Y2) or autosome trivalents (g/o and m/q) was detected at diakinesis-metaphase I. Two hybrids displayed a theoretically expected and unimpaired meiotic configuration in a form of a very long chain comprising 11 monobrachial homologs (g/gm/mq/qp/pr/rk/ki/ih/hn/no/o). The results are discussed in terms of hypotheses on fertility of complex heterozygotes and limited gene flow in hybrid zone.     

The role of chromosome rearrangements in evolution of mole voles of genus Ellobius (Rodentia, Mammalia)

Modern mole voles of the genus Ellobius are characterized by species-specific features of autosomes and sex chromosomes. Owing to the use of the Zoo-FISH method, the nomenclature of chromosomes was refined and nonhomologous Robertsonian translocations indistinguishable by G-staining were identified for Ellobius tancrei, which is a species with a wide chromosome variation of the Robertsonian type. The electron-microscopic analysis of synaptonemal complexes in F1 hybrids of forms with 2n = 50 and 2n = 48 revealed the formation of a closed SC-pentavalent composed of three metacentrics with monobrachial homology and two acrocentrics. Segregation of chromosomes of such complex systems is impeded by disturbances in the nucleus architecture leding to the formation of unbalanced gametes and to a dramatic reduction in fertility of hybrids. Our data support the hypothesis that the formation of monobrachial homologous metacentric chromosomes can be considered as a way of chromosomal speciation.     

Meiotic drive favors Robertsonian metacentric chromosomes in the common shrew (Sorex araneus, Insectivora, mammalia)

Meiotic drive has attracted much interest because it concerns the robustness of Mendelian segregation and its genetic and evolutionary stability. We studied chromosomal meiotic drive in the common shrew (Sorex araneus, Insectivora, Mammalia), which exhibits one of the most remarkable chromosomal polymorphisms within mammalian species. The open question of the evolutionary success of metacentric chromosomes (Robertsonian fusions) versus acrocentrics in the common shrew prompted us to test whether a segregation distortion in favor of metacentrics is present in female and/or male meiosis. Performing crosses under controlled laboratory conditions with animals from natural populations, we found a clear trend toward a segregation distortion in favor of metacentrics during male meiosis, two chromosome combinations (gm and jl) being significantly preferred over their acrocentric homologs. Apart for one Robertsonian fusion (hi), this trend was absent in female meiosis. We propose a model based on recombination events between twin acrocentrics to explain the difference in transmission ratios of the same metacentric in different sexes and unequal drive of particular metacentrics in the same sex. Pooled data for female and male meiosis revealed a trend toward stronger segregation distortion for larger metacentrics. This is partially in agreement with the frequency of metacentrics occurring in natural populations of a chromosome race showing a high degree of chromosomal polymorphism.     

Complex sex chromosome system in Eigenmannia sp. (Pisces,Gymnotiformes)

Chromosomes of Eigenmannia sp. (7 males and 15 females) collected from the Tietê River in Botucatu (SP, Brazil) were examined from gill, kidney and testicular cells. The diploid chromosome number in males was 2n=31 and in females, 2n=32. In both sexes the number of chromosomal arms was 40. The difference in diploid number was due to the fusion of two acrocentrics. Mitotic and meiotic studies suggested that one of the fused acrocentrics was the Y chromosome. The sex-determining mechanism in Eigenmannia sp. could therefore be XX, AA in the female and X, \-YA A in the males. One of the males presented 2n=30 chromosomes due to the occurrence of another fusion of acrocentrics. C-banding analysis of the mitotic chromosomes revealed constitutive heterochromatin in the centromeric regions of all acrocentrics. However, small metacentrics were C-band negative. The YA chromosome is C-band negative except for a small amount of heterochromatin in the centromeric region. The nucleolar organizer region as identified by Ag-staining is present in the interstitial region of chromosome pair No. 10.     

Factors Affecting Recognition and Disjunction of Chromosomes at Distributive Pairing in Female DROSOPHILA MELANOGASTER. I. Total Length VS. Arm Length

The behavior of a compound metacentric fourth chromosome (see PDF) has been examined to determine whether arm length or total length is the basis for recognition in distributive pairing. Recognition was judged by the frequency with which the (see PDF) nondisjoined from a series of X duplications (Dp), ranging in size from ≤ 0.3 to > 4 times the size of a single fourth chromosome. Dp, (see PDF) nondisjunction was measured in the absence and in the presence of a competitor, a compound metacentric X. In both situations, total length and not arm length, was found to confer the characteristic recognition property to the (see PDF). A comparison of Dp, (see PDF) nondisjunction curves for both the noncompetitive and competitive situations with analogous Dp, 4 curves previously obtained, show the Dp, (see PDF) curves to be similar in shape to those obtained earlier but displaced one unit to the right, corresponding precisely to the difference in size between the (see PDF) and the 4. Rules governing chromosome recognition for acrocentrics were found completely applicable to metacentrics; disjunctive behavior of metacentrics differed from that of acrocentrics in that two arms conferred on a chromosome the capacity to act as the intermediate of a trivalent when size no longer warranted this attribute. This capacity, itself, is size-dependent.     

Chromosome polymorphism in the ant,Pheidole nodus

A survey of chromosome polymorphism was made in populations of Pheidole nodus (Hymenoptera, Formicidae). A total of 1,666 males were collected from 11 localities in Japn. Four polymorphic karyotypes were observed: (1) n = 17 with 4 metacentrics (abbreviated as 4M), (2) n = 18(3M), (3) n = 19(2M) and (4) n = 20(1M). These differences are due to the Robertsonian type rearrangement. The karyotype 18(3M) is found in all the populations examined, but the others are more or less localized in their distribution. The 17(4M) appears mainly in Shikoku and the northern Kyushu populations, 19(2M) along the Pacific coast of Honshu, Shikoku and Kyushu, and 20(1M) in the eastern part of Honshu and Shikoku. This distribution pattern indicates that 18(3M) is the oldest, 19(2M) and 20(1M) are derived from 18(3M) by centric fission, and 17(4M) by centric fusion. The most probable mechanism of karyotype evolution in this species is considered to be the centric fission.     

Cytogenetic characterization of two species of Frieseomelitta Ihering, 1912 (Hymenoptera, Apidae, Meliponini)

The cytogenetic analysis of Frieseomelitta dispar and F. francoi revealed the chromosome numbers 2n = 30 and n = 15 and a karyotypic formula 2K = 4M+2M(t)+4A+20A(M). The number of chromosomes observed was consistent with those reported for other Frieseomelitta species. The occurrence of the M(t) chromosome and other features of the karyotype formulae suggest a close relationship between F. dispar, F. francoi and F. varia. Nevertheless, it was possible to differentiate the karyotypes of the species by DAPI/CMA(3) staining, which revealed GC-rich regions on two chromosome pairs of F. dispar: one acrocentric and one pseudoacrocentric. In F. francoi, the same kinds of regions were observed on a pair of metacentrics and on a pair of acrocentrics. Our analysis also confirmed the chromosome number conservation in Frieseomelitta and suggests that infrequent pericentric inversion could constitute a synapomorphy for the group including F. dispar, F. francoi, and F. varia.     

Variation and Evolution in the Karyotype of Lycoris (Amaryllidaceae) V. Chromosomal Variation in L. sanguinea Maxim.

Abstract In 554 bulbs from 38 populations of Lycoris sanguinea , several chromosomal variations have been discovered. Most of the bulbs have a common karyotype consisting of 22 acrocentric ( A ) chromosomes. Though their frequencies are low, some rearranged chromosomes which are aberrant have been found. The aberrants are as follows: 1. Subtelocentrics ( ST ); 2. Telocentrics ( T' ); 3. Metacentrics ( M' ); 4. Very small acrocentrics (a); 5. Very small metacentrics (m); 6. Acentric fragments ( Ac ); and 7. Dicentrics ( Di ) chromosome. All can be easily suspected to be derived from A s. Some aberrations of the satellite chromosomes have been observed also. In addition, a new karyotype composed of 2n=32=31 A + 1 M' chromosomes has been found.     

Chromosomal variation and evolution in Lycoris (Amaryllidaceae) I. Intraspecific variation in the karyotype of Lycoris chinensis Traub

In 188 bulbs from five populations of Lycoris chinensis from Anhui province, China, several chromosomal variations have been discovered. Although their frequencies are low, some rearranged chromosomes which are aberrant have been found. The aberrants are: (1) small metacentrics (m′); (2) submetacentrics (sm); (3) subtelocentrics (st); (4) acrocentrics (t); and (5) satellite chromosomes (SAT). All can be easily suspected as being derived from telocentric chromosomes (T type chromosomes). Some individuals having one or more B chromosomes have been found, and intrapopulational variation of B chromosomes in number has also been observed. Because of having B chromosome, L. chinensis has some different chromosome complement numbers: 2n?=?16, 2n?=?16?+?1B, 2n?=?16?+?2B, 2n?=?16?+?3B, and 2n?=?16?+?5B. In addition, a new triploid karyotype composed of 3n?=?24?=?9m?+?11t(2SAT)?+?4T chromosomes has been found. Vegetative propagation is an efficient means of perpetuating the aberrant chromosomes and the triploids.     

Sex chromosome evolution in fish: the formation of the neo-Y chromosome in Eigenmannia (Gymnotiformes)

Chromosomes of a species of Eigenmannia presenting a X₁X₁X₂X₂:X₁X₂Y sex chromosome system, resulting from a Y-autosome Robertsonian translocation, were analyzed using the C-banding technique, chromomycin A₃ (CMA₃) and mithramycin (MM) staining and in situ digestion by the restriction endonuclease AluI. A comparison of the metacentric Y chromosome of males with the corresponding acrocentrics in females indicated that a C-band-positive, CMA₃/MM-fluorescent and AluI digestion-resistant region had been lost during the process of translocation, resulting in a diminution of heterochromatin in the males. It is hypothesized that the presence of a smaller amount of G+C-rich heterochromatin in the sex chromosomes of the heteromorphic sex when compared with the homomorphic sex may be associated with the sex determination mechanism in this species and may be a more widely occurring phenomenon in fish with differentiated sex chromosomes than was initially thought. Received: 1 April 1999; in revised form: 16 October 1999 / Accepted: 4 December 1999     

Heteromorphic sex chromosomes of lizardfish (Synodontidae): focus on the ZZ-ZW1W2 system in Trachinocephalus myops

The karyotype and DNA content of four lizardfish species (family Synodontidae), that is, Saurida elongata, Synodus ulae, Synodus hoshinonis and Trachinocephalus myops, were analyzed. The karyotype of T. myops significantly differed from that of the other three species having diploid chromosome number of 48 with mainly acrocentric chromosomes and the ZZ-ZW sex chromosome system. The chromosome number of male T. myops was 2n=26, while that of female T. myops was 2n=27. The karyotype consisted of 11 pairs of metacentrics, one pair of acrocentrics and, in addition, two large metacentrics in the male and a single large metacentric, a distinctly small subtelocentric and a microchromosome in the female. C-banding demonstrated that in the female the subtelocentric chromosome and the microchromosome were heterochromatic. The karyotype of T. myops was thought to be derived from a 48 chromosome type synodontid fish through the involvement of Robertsonian rearrangement; the rearrangement of the sex chromosomes proceeded during karyotype evolution. Among the chromosomes, the large metacentrics were determined to be neo-Z (a fusion of the original Z and an autosome), the microchromosomes the W₁ (originally W), and the subtelocentric chromosomes the W₂ (derived from an autosome pair). The miniaturization of W₁ and W₂ chromosomes and their heterochromatinization suggested that sex chromosomes in this species have been already highly differentiated. The findings on DNA content implied that the karyotype of T. myops evolved by centric fusion events without loss in DNA amount.     

Cosegregation of Robertsonian metacentric chromosomes in the first meiotic division of multiple heterozygous male mice as revealed by FISH analysis of spermatocyte II metaphases

Contrasting results (random segregation or cosegregation of isomorphic chromosomes) have been reported up to now on the segregation pattern of Robertsonian metacentric chromosomes of Mus musculus domesticus in multiple heterozygotes, using different approaches (karyotypical analysis of the progeny or of second meiotic metaphases). In the present contribution data are presented based on FISH (Fluorescence In Situ Hybridisation) analysis with telomeric probes, which allowed us to distinguish metacentric chromosomes from pairs of acrocentric chromosomes with their centromeric regions close to each other. Probes were hybridized to DAPI stained metaphases of spermatocytes II of mice heterozygous for two, three or four Robertsonian metacentrics in an all-acrocentric background, the karyotype of which has been reconstructed starting from laboratory strains. Isomorphic chromosomes tend to cosegregate (metacentrics with metacentrics, acrocentrics with acrocentrics); the values found for cosegregation have a clear even if moderate effect on the reproductive isolation caused by underdominant chromosomal rearrangements.