The B-chromosome in the karyotype of Tetrix tenuicornis (Sahlb.) (Tetrigidae: Orthoptera)

B-chromosomes were observed in a Polish natural population of Tetrix tenuicornis. Three males showed a mitotically unstable and probably acrocentric B-chromosome, similar in size to the sex chromosome. In one specimen two forms of the B-chromosome occurred in various combinations (i.e. 6A+X; 6A+B; A; 6A+X+B; 6A+X+2B).     

B-chromosome behaviour in Phaulacridium vittatum

Nine individuals of Phaulacridium vittatum in a single population sample of 1250 males collected at Crookwell, N. S.W. contained a single supernumerary chromosome. One further individual had two B-chromosomes. The supernumerary in question was larger than any of the standard set and was distinguishable from them at all stages of mitosis and meiosis. Like the X-univalent the B-chromosome was heteropycnotic at the onset of meiosis but differed from it in size, structure and behaviour. During first prophase single supernumeraries were frequently associated with the X in a non-homologous fashion as a consequence of their precocity. All such associations lapsed before first metaphase and the X and the B moved at random with respect to one another at first anaphase. In the one individual with two supernumeraries the two B-chromosomes showed regular pairing and segregated in a conventional manner. In all these respects the Crookwell supernumerary differed markedly from a morphologically identical B-chromosome present in a population of the same species from Hobart, Tasmania studied by Jackson and Cheung in 1967. Whether these differences in the behaviour of the B-chromosome in the two populations determines the higher frequency of the supernumerary in Hobart (11.3%) as compared with Crookwell (0.8%) remains to be resolved.     

Interpopulation variation in the satellite DNA from grasshoppers with B-chromosomes

When run on a CsCl gradient the DNA from individuals containing B-chromosomes reveals a satellite peak in addition to the main DNA peak found in individuals without B-chromosomes. This was shown in several populations of grasshoppers. This B-chromosome DNA contains 28% repeated and 72% unique sequences as determined by hydroxyapatite chromatography. This was shown to be the case in two of the populations. The really surprising observation was that the repeated nucleotide sequences of the B-chromosome DNA have no apparent homology in this single species of grasshopper. This was demonstrated by the lack of hybridisation between labelled C-RNA transcribed from one B-chromosome DNA and the DNA from the B-chromosome peak from another population. This lack of homology was also suggested by density differences between B-chromosome satellites in CsCl gradients. Furthermore, there was no sequence homology between the satellite (B-chromosome) DNA and the main peak (nuclear) DNA.     

The cytogenetic structure of Tasmanian populations of Phaulacridium vittatum

In 8 out of 20 Tasmanian populations of Phaulacridium vittatum from 0.3-11.0 percent of the males carried a single supernumerary chromosome. In such males the X and B univalents are both heteropycnotic at first prophase of male meiosis and associate with another in a non-homolgous manner in about two-thirds of the diplotene cells examined. In all 56 B-containing individuals studied, however, these associations lapse by first metaphase and the X and the B move at random with respect to one another at first anaphase. The supernumerary in this species is stable and only 5 of the 56 individuals with supernumeraries showed evidence of B-chromosome non-disjunction in the pre-meiotic mitoses. Since there was no other evidence for the loss or gain of supernumeraries in the male line it is clear that B-transmission is regular in the males of this species. There were significant differences between population with respect to mean cell chiasma frequency but there was no significant effect of the B-chromosome on this metric. Additionally a comparison of mean cell chiasma frequency in follicles with and without supernumeraries from a mosaic individual shows no significant difference.     

Segregation-distortion in the B-chromosome system ofTettigidea lateralis (say) (Orthoptera: Tetrigidae)

A marginal population ofTettigidea lateralis was found to be polymorphic with respect to a large, mitotically stable supernumerary (B) chromosome. Male and female individuals may carry one or two B-chromosomes. In the male sex the frequency of individuals with one B was 33.8% whereas that of 2B-carriers was 2.9 %. A comparison with a small sample of female individuals suggests similar frequencies of B-chromosome carriers in the two sexes. The pycnocity cycle of the B's is virtually identical to that of the X chromosome which is always distinguishable by virtue of its larger size and other structural details. Persistent heterochromatic associations between the B and the X, which may last until metaphaseanaphase I, lead to a preferential migration of the B with the X to the same pole in male carriers of a single supernumerary. This distortional segregation of the B-chromosome may produce a differential transmission of the supernumerary to the two sexes if the various types of gametes are equally functional. Achiasmate, persistent B-B associations in 2B individuals can also cause segregation-distortion. The two supernumeraries segregate to the same pole in approximately 1/3 of the spermatocytes, but their poleward movement relative to that of the X is random. Both –B and +B individuals show only a single chiasma per individual bivalent. However, the presence of a single B raises very significantly the frequency at which the chiasma forms at the extreme distal ends of the L₁-L₂ and M₃-M₄ autosomes. The effect on recombination exerted by the supernumeraries and the possible implications of the segregation-distortion system ofT. lateralis are discussed in the light of recent studies on comparable B-chromosome polymorphisms.Research supported by N.R.C. of Canada.     

The B-chromosome system of myrmeleotettix maculatus (thunb.)

It is established that in populations of Myrmeleotettix maculatus with B-chromosomes these chromosomes occur at stable frequencies and are present to the same extent in both the males and the females of the same population. It is also established that the B-chromosome content of a population is positively correlated with its chiasma frequency and that, within a population, individuals with single B-chromosomes tend to have higher chiasma frequencies than individuals lacking B-chromosomes. Since this effect is not increased by the addition of further supernumeraries it is argued that selection operates in favour of individuals with single B-chromosomes. Finally it is shown that the level of B-chromosomes in a population is related to temperature and especially to rainfall so that B-chromosomes are absent from populations in climatically stringent environments.     

Stability of the population variants of the B-chromosome system in the East-Asian mouse Apodemus peninsulae from the Baikal region and Northern Mongolia

Analysis of the B-chromosome frequency and morphotypes in 160 mice Apodemus peninsulae from 17 localities of the Baikal region, Northern Mongolia, Trans-Baikalia, and the Russian Far East showed that the mice were from five geographical populations. The interpopulation difference was determined by variations of 0?C4 macro B chromosomes and 0?C11 micro B chromosomes. The B-chromosome number and morphotypes proved to be stable over the past 30 years in the geographical populations under study.     

B-chromosome evolution

B chromosomes are extra chromosomes to the standard complement that occur in many organisms. They can originate in a number of ways including derivation from autosomes and sex chromosomes in intra- and interspecies crosses. Their subsequent molecular evolution resembles that of univalent sex chromosomes, which involves gene silencing, heterochromatinization and the accumulation of repetitive DNA and transposons. B-chromosome frequencies in populations result from a balance between their transmission rates and their effects on host fitness. Their long-term evolution is considered to be the outcome of selection on the host genome to eliminate B chromosomes or suppress their effects and on the B chromosome's ability to escape through the generation of new variants. Because B chromosomes interact with the standard chromosomes, they can play an important role in genome evolution and may be useful for studying molecular evolutionary processes.     

Variable transmission rates of a B-chromosome in Myrmeleotettix maculatus (Thunb.) (Acrididae: Orthoptera)

Karyotype comparisons of both parents and progeny from single pair matings in the grasshopper Myrmeleotettix maculatus have shown that there is an accumulation of the large mitotically stable B-chromosome when transmitted through the female. This is presumed to result from a preferential segregation of univalent B-chromosomes at the first division of female meiosis and occurs irrespective of whether the B's are odd or even in number. In the male there is a loss of B-chromosomes. This loss does not appear to be due simply to the lagging and elimination of B-chromosomes in meiosis but probably involves sperm formation or function. When the balance of the gain and loss after one generation is calculated, it shows large overall accumulation in crosses involving individuals from a population in Wales, and a slight loss in individuals from a population in East Anglia. Such differences in transmission rates may be responsible for differences in B-frequency between populations. Since the B-chromosome frequency of these two populations has remained stable over five years, possible forces in the maintenance of the equilibria are examined. Females with B-chromosomes produce more aneuploid embryos than 0B females, but neither this cause of inviability nor general embryo mortality seem sufficient to produce an equilibrium situation. It is necessary to postulate that progeny with more than 2B chromosomes are inviable in order to approach equilibria. The presence of B-chromosomes in females has also led to the formation of polyploid embryos. The possible involvement of repetitive DNA in the formation of unreduced egg nuclei and preferential segregation is discussed.     

Phyletic hot spots for B chromosomes in angiosperms

We determined whether supernumerary B chromosomes were nonrandomly distributed among major angiosperm lineages and among lineages within families, as well as the identity of lineages with unusually high B-chromosome frequencies (hot spots). The incidence of B chromosomes for each taxon was gathered from databases showing species with and without these chromosomes (among species with known chromosome numbers). Heterogeneity was found at all ranks above the species level. About 8% of monocots had B chromosomes versus 3% for eudicots; they were rare in nonmonocot basal angiosperms. Significant heterogeneity in B-chromosome frequency occurred among related orders, families within orders, and major taxa within families. There were many B-chromosome hot spots, including Liliales and Commelinales at the order level. At the family level, there was a trend suggesting that B-chromosome frequencies are positively correlated with genome size.     

Host recombination is dependent on the degree of parasitism

Parasites and hosts are involved in a continuous coevolutionary process leading to genetic changes in both counterparts. To understand this process, it is necessary to track host responses, one of which could be an increase in sex and recombination, such as is proposed by the Red Queen hypothesis. In this theoretical framework, the inducible recombination hypothesis states that B-chromosomes (genome parasites that prosper in natural populations of many living beings) elicit an increase in host chiasma frequency that is favoured by natural selection because it increases the proportion of recombinant progeny, some of which could be resistant to both B-chromosome effects and B-accumulation in the germline. We have found a clear parallelism between host recombination and the evolutionary status of the B-chromosome polymorphism, which provides explicit evidence for inducible recombination and strong support for the Red Queen hypothesis.     

A Preliminary Observation on B-Chromosomes of Regal lily

The authors have observed t he karyotypes of the Regal Lily with B-chromosome and without B-chromosomes as well as their Giemsa C-bands. The results show that the karyotypes with B-chromosomes are not obviously different from those without B- chromosomes. B-chromosome is additional and all of them are heterochromatization. But segregation of B-chromosome at anaphase Ⅰ and Ⅱ in meiosis is irregular, and about half of the pollen grains contain B-chromosomes. In the progenies by open pollination the segre, gation of 0B and lB appear in the ratio near 1:1 and the offsprings with 2B-chromosomes only average 2.6 percent.     

B chromosome ancestry revealed by histone genes in the migratory locust

In addition to the standard set of chromosomes (A), about 15% of eukaryote genomes carry B chromosomes. In most cases, B chromosomes behave as genomic parasites being detrimental for the individuals carrying them and prospering in natural populations because of transmission advantages (drive). B chromosomes are mostly made up of repetitive DNA sequences, especially ribosomal DNA (rDNA), satellite DNA and mobile elements. In only two cases have B chromosomes been shown to carry protein-coding genes. Although some B chromosomes seem to have derived from interspecific hybridisation, the most likely source of B chromosomes is the host genome itself, but the specific A chromosome being the B ancestor has not been identified in any B-containing species. Here, we provide strong evidence for B chromosome ancestry in the migratory locust, based on the location of genes for the H3 and H4 histones in the B chromosome and a single A chromosome pair (i.e. the eighth in order of decreasing size). The high DNA sequence similarity of A and B chromosome H3–H4 genes supports B-origin from chromosome 8. The higher variation shown by B sequences, compared to A sequences, suggests that B chromosome sequences are most likely inactive and thus less subjected to purifying selection. Estimates of time of divergence for histone genes from A and B chromosomes suggest that B chromosomes are quite old (>750,000 years), showing the B-chromosome ability to persist in natural populations for long periods of time.     

The nature and behaviour of supernumerary chromosomes in the rhizirideum group of the genus Allium

Individuals at various levels of ploidy in three species of Allium (angulosum, nutans and senescens) contain a morphologically uniform B-chromosome. This supernumerary is different in character from other B-types recorded for the genus. In diploids the B divides at second anaphase so that 50% of the pollen grains transmit it. The level of transmission is lower in the pollen of polyploids and still lower on the female side where pre-meiotic elimination occurs in both diploids and polyploids. Despite this, and although no effect of the B could be discerned on germination, all plants examined possessed the B-chromosome.This paper was prepared in the Department of Genetics, University of Birmingham while the author was a recipient of a British Council Scholarship.     

The conflict between natural and artificial selection in finite populations

Summary A single locus model of the interaction between natural selection and artificial selection for a quantitative character in a finite population, assuming heterozygote superiority in natural fitness but additive action on the character, has been studied using transition probability matrices.If natural selection is strong enough to create a selection plateau in which genetic variance declines relatively slowly, then the total response to artificial selection prior to the plateau will be much less than that expected in the absence of natural selection, and the half-life of response will be shorter. Such a plateau is likely to have a large proportion, if not all, of the original genetic variance still present. In selection programmes using laboratory animals, it seems likely that the homozygote favoured by artificial selection must be very unfit before such a plateau will occur. A significant decrease in population fitness as a result of artificial selection does not necessarily imply that the metric character is an important adaptive character.These implications of this model of natural selection are very similar to those derived by James (1962) for the optimum model of natural selection. In fact, there seems to be no aspect of the observable response to artificial selection that would enable anyone to distinguish between these two models of natural selection.     

The clinal variability of the B-chromosome system in the East Asian mouse Apodemus peninsulae from Buryatia and Mongolia]

Karyological investigation of 22 East-Asiatic mice from different points of the North Mongolia showed the availability in all the mice from 1 to 13 B chromosomes, including from 1 to 5 middle-sized and small two-shoulder chromosomes, from 0 to 11 dot-like B chromosomes, and, seldom, 1 small acrocentric B chromosome. Nearly every mouse is characterized by its variant of B-chromosome system. Most frequent mice with 3, 4 and 8 B chromosomes were met. The comparison of the B-chromosome system variants in mice from Buryatia, Chita Province (USSR) and the North Mongolia, showed an increase in the number of B chromosomes, mainly at the expense of the number of dot-like B chromosomes, in the direction from Ulan-Ude to the south and to the east.     

Origin and molecular organization of supernumerary chromosomes of Prochilodus lineatus (Characiformes, Prochilodontidae) obtained by DNA probes

In Prochilodus lineatus B-chromosomes are visualized as reduced size extra elements identified as microchromosomes and are variable in morphology and number. We describe the specific total probe (B-chromosome probe) in P. lineatus obtained by chromosome microdissection and a whole genomic probe (genomic probe) from an individual without B-chromosome. The specific B-chromosome was scraped and processed to obtain DNA with amplification by DOP-PCR, and so did the genomic probe DNA. Fluorescence in situ hybridization using the B-chromosome probe labeled with dUTP-Tetramethyl-rhodamine and the genomic probe labeled with digoxigenin-FITC permitted to establish that in this species supernumerary chromosomes with varying number and morphology had different structure of chromatin when compared to that of the regular chromosomes or A complement, since only these extra elements were labeled in the metaphases. The present findings suggest that modifications in the chromatin structure of B-chromosomes to differentiate them from the A chromosomes could occur along their dispersion in the individuals of the population.     

Population dynamics of a selfish B chromosome neutralized by the standard genome in the grasshopper Eyprepocnemis plorans

Effects of the B chromosome polymorphism of the grasshopper Eyprepocnemis plorans were analyzed in two natural populations. Postmating sexual selection, female fertility, and survival were studied. The B chromosome lacks drive and has no detectable effects on fitness. A neutral B cannot invade a population and establish a polymorphism, but the confidence limits on our estimates cannot exclude the possibility that the polymorphism is maintained by a balance between weak drive and weak selection against individuals with two and three B's. However, other lines of evidence favor the following model of the dynamics of the B in E. plorans. In a newly invaded population, the B has substantial drive, but the evolution of drive suppressor genes in the A chromosomes neutralizes the B drive so that it becomes near-neutral and begins a random walk toward extinction by stochastic loss. Because the B is common by the time drive disappears, the random walk is likely to continue for a long time. If in the course of the random walk a variant B with greater drive appears, then it will displace the original variant, and a new cycle of drive suppression and drift to extinction occurs. A simulation model of this process suggested that the mean time to extinction is proportional to the two-thirds power of the population size; it is much less affected by subpopulation size or the number of populations in a subdivided population.     

Cytogenetics of collared lemmings (Dicrostonyx groenlandicus). II. Meiotic behavior of B chromosomes suggests a Y-chromosome origin of supernumerary chromosomes

The patterns of synapsis and chiasma formation of the B chromosomes of male collared lemmings (Dicrostonyx groenlandicus) were analyzed by light and electron microscopy and compared to expectations for various hypotheses for the intragenomic origin of supernumerary chromosomes. Pachytene analysis revealed a variety of synaptic configurations including B-chromosome univalents, bivalents and trivalents. In approximately one-half of the pachytene nuclei examined, B chromosomes were in synaptic associations with the normally unpaired portion of the Y chromosome. The B-chromosome configurations at pachynema, including those involving the Y chromosome, were maintained into diakinesis and metaphase I. The meiotic behavior of the B chromosomes was inconsistent with their derivation from centric-fusion products, isochromosome formation, small-autosome polysomy, or the X chromosome. However, the frequent synapsis and apparent recombination between B chromosomes and the Y chromosome implicate this sex chromosome as a possible source of the B chromosomes in collared lemmings.