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.     

Phylogeography of the Russian flying squirrel (Pteromys volans): implication of refugia theory in arboreal small mammal of Eurasia

A phylogeographical study of the Russian (Siberian) flying squirrel (Pteromys volans) was carried out using the complete mitochondrial (mt) cytochrome b gene sequences with special reference to the refugia theory for the arboreal traits of this species. We examined 31 specimens from 24 localities, resulting in 28 haplotypes. One breeding specimen with a unique haplotype from Hokkaido, Japan was included in the phylogenetic analysis. There were three mtDNA lineages: Hokkaido, Far Eastern, and northern Eurasia. Divergence data among lineages demonstrated that the Hokkaido group separated from the other groups during the Holsteinian interglacial. The phylogeographical pattern of P. volans is different from that previously reported for terrestrial rodents associated with treeless habitats. Unlike grasslands, forests decreased during glaciation and moved southward because of the cold and arid environmental conditions. The glacial refugia of P. volans would have been associated with forest dynamics in the Pleistocene.     

B chromosomes of the Podisma sapporensis Shir. (Orthoptera, Acrididae) analysed by chromosome microdissection and FISH

The analysis of the distribution of repetitive DNA of the B chromosomes of Podisma sapporensis in the A and B chromosomes of the natural populations and in A chromosomes of three other species of the Podismini grasshoppers were made. DNA-libraries of the B chromosome and the euchromatic segment of the A chromosome of P. sapporensis were generated by meiotic chromosome microdissection followed by degenerated oligonucleotide primed polymerase chain reaction (DOP-PCR). Paints based on these DNA-libraries were used for FISH analysis to detect localization of homologous sequences in A and B chromosomes of P. sapporensis from different natural populations. On the basis of the FISH analysis the authors suggest that evolution of the B chromosomes in Podisma sapporensis was associated mainly with the insertions of "alien DNA sequences" into ancestral A chromosome and their further amplification. The number of initial sites of amplifications differed in the different Bs, the distance between these sites also varying. Karyotype evolution in P. sapporensis was associated partly with the insertion of "alien DNA sequences" into pericentromeric chromosomal regions. Insertion into the small short arms of the acrocentric chromosomes followed, with the DNA amplification leading to the formation of the additional C-heterochromatic arms or euchromatic-like regions of different size.     

Effect of a rye B chromosome and its segments on homoeologous pairing in hybrids between common wheat and Aegilops variabilis

Rye B chromosomes, which are supernumerary chromosomes dispensable for the host but increase in number by non-disjunction after meiosis, have been reported to affect meiotic homoeologous pairing in wheat-rye hybrids. The effect of a rye B chromosome (B) and its segments (B-9 and B-10) on homoeologous pairing was studied in hybrids between common wheat (2n=42) and Aegilops variabilis (2n=28), with reference to the Ph1 gene located on wheat chromosome 5B. The B-9 and B-10 chromosomes are derived from reciprocal translocations between a wheat and the B chromosomes, and the former had the B pericentromeric segment and the latter had the B distal segment. Both the B and B-9 chromosomes suppressed homoeologous pairing when chromosome 5B was absent. On the other hand, the B-9 and B-10 chromosomes promoted homoeologous pairing when 5B was present. On pairing suppression, B-9 had a greater effect in one dose than in two doses, and B-9 had a greater effect than B-10 had in one dose. These results suggested that the effect of the B chromosomes on homoeologous pairing was not confined to a specific region and that the intensity of the effect varied depending on the presence or absence of 5B and also on the segment and dose of the B chromosome. The mean chiasma frequency (10.23) in a hybrid (2n=36) possessing 5B and one B-9 was considerably higher than that (2.78) of a hybrid (2n=35) possessing 5B alone, and was comparable with that (14.09) of a hybrid (2n=34) lacking 5B. This fact suggested that the B chromosome or its segment can be used in introducing alien genes into wheat by inducing homoeologous pairing between wheat and alien chromosome.     

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.     

蜘蛛的B染色体研究——Ⅰ.武汉地区粽管巢蛛的B染色体(蜘蛛目:管巢蛛科)

首次发现武汉地区粽管巢蛛胚胎细胞中存在B染色体,观察数目为1～28条,B染色体数目从有丝分裂晚前期到中期逐渐减少,在非整倍体细胞中,随着A染色体的减少逐渐增多。B染色体形态稳定;大多数为等臂染色体,少数具亚端着丝点和端着丝点;外观上明显小于A染色体。     

Evolution of a complex B-chromosome polymorphism in the grasshopper Eyprepocnemis plorans

B-chromosome systems in several Spanish natural populations of Eyprepocnemis plorans are reported. The geographical distributions of the fourteen types of B chromosomes, which were classified according to size, C-banding pattern, and meiotic behaviour, are described. The results indicate a common origin for most types and a possible independent origin for a few secondary B variants. The origin and mechanisms of evolution of this B chromosome polymorphism are discussed.     

大林姬鼠的核型与B染色体研究

采用骨髓染色体制片法 ,对分布于吉林长白山、山东泰山和陕西秦岭的大林姬鼠的染色体组型、C -带、G -带和减数分裂的染色体行为进行了观察分析。发现 3个地区标本的染色体数目存在着显著差异。东北标本的 2n =48～ 51 ,A组染色体为 48条 ,均由端着丝粒染色体组成 ,同时具有 1～ 3条B染色体 ,其形态为中着丝粒染色体 ;山东标本的 2n =53～ 62 ,A染色体同样为 48条端着丝粒染色体组成 ,具 5～ 1 4条B染色体 ,其中 1条为较大的中着丝粒染色体 ,其余为小的中着丝粒和点状染色体。秦岭标本 2n =48～ 49,A染色体为 48条端着丝粒染色体 ,具 1条形态很小的端着丝粒B染色体。3地标本的B染色体均存在个体间和个体内变异。长白山标本B染色体的细胞克隆数目为 1～ 2 ,泰山标本为 1～ 3。在 3地标本中 ,中着丝粒B染色体呈现C -带阴性 ,点状B染色体呈中度深染。通过对减数分裂的观察 ,多数B染色体是以单价体的形式存在。中国长白山种群的B染色体数目和形态与朝鲜种群相似。与欧洲种群存在着显著差异。泰山种群的B染色体数目和形态与朝鲜种群及欧洲种群均存在显著差异。泰山种群与秦岭标本同属华北亚种 ,但它们的B染色体形态和数目差别很大。     

Comparative FISH analysis of distribution of B chromosome repetitive DNA in A an d B chromosomes in two subspecies of Podisma sapporensis (Orthoptera, Acrididae)

FISH analysis of B chromosome repetitive DNA distribution in A and B chromosomes of two subspecies of Podisma sapporensis (P. s. sapporensis and P. s. krylonensis) was performed. In the B chromosomes, C-positive regions contained homologous DNA repeats present also in some C-positive A chromosome regions. Most C-negative regions contained DNA repeats characteristic of A chromosome euchromatic regions. The two subspecies analyzed differed in the location of A chromosome regions enriched with repeats homologous to repeats of B chromosomes. The only common region enriched with these B chromosome repeats in both subspecies was the X chromosome pericentromeric region. The origin of B chromosomes in P. sapporensis is discussed.     

B chromosome variation in Euphydryas colon (Lepidoptera: Nymphalidae)

Cytogenetic analysis of an Idaho population of the checkerspot butterfly, Euphydryas colon, has revealed considerable inter- and intra-individual variation in chromosome number which turns out to be a classic case of B chromosome variation. The basic chromosome complement of the species is n (, )=31. The A chromosomes were aligned equatorially at mitotic metaphase and metaphase II, and axially at metaphase I, indicating a restriction of centric activity at the first meiotic division. No failure of pairing between homologous A chromosomes was observed and, although a marked asynchrony of chromatid separation was found to be characteristic of mitotic telophase and telophase II, the frequency of macrospermatid formation was low. The B chromosomes were at least partly heterochromatic but exhibited some variation in both pycnosity and size. Mitotically stable B-containing individuals showed a preponderance of unpaired Bs at first metaphase and these divided at either first or second anaphase. The presence of Bs was associated with a heightened production of abnormal spermatids particularly in individuals with high numbers of B chromosomes. Among the 25 individuals sampled, 21 carried from 1–6 B chromosomes, and of these 14 were mitotically stable. In all 7 unstable individuals the mean number of B chromosomes per cell exceeded the modal number. Assuming that the modal number represents the zygotic number, these results suggest that a mechanism to boost the number of B chromosomes exists in males of E. colon.     

Karyological studies on Picea ajanensis (Lindl. et Gord.) Fisch. ex Carr. from different regions

Results of karyological study of Picea ajanensis (Lindl. et Gord.) Fisch. ex Carr examined from 13 provenances are presented. In addition to the cytotypes with typical chromosome number (2n = 24), P. ajanensis displays cytotypes with one or two B-chromosomes (2n = 24 + 1 - 2B). Among A-chromosomes, there are 8 pairs of long metacentrics and 4 pairs of shorter meta- or submetacentrics. Among B-chromosomes there are two types of chromosomes: metacentric (B1) and submetacentric (B2) ones. There are many nucleolar chromosomes. Several chromosomes have secondary constrictions. Patterns of B-chromosome distribution within P. ajanensis are have been discussed.     

Polymorphism and mosaicism of B chromosome number in Korean field mouse <Emphasis Type="Italic">Apodemus peninsulae</Emphasis> (Rodentia) in the Russian Far East

A karyotype analysis of the Apodemus peninsulae (n = 355) from 41 trapping points from the Russian Far East has allowed us to identify B chromosomes in 87.9% of the animals, 61.7% of which are mosaics. Different levels of variability in the B chromosome numbers have been studied, including both the inter- and intrapopulational, as well as intraindividual variability (mosaicism). It was found that the frequencies of the occurrence of individuals with B chromosomes and mosaicism between different population samples were not constant. The range of the modal B chromosome number variability and variation of the xB index (zero to four; on average, the xB amounted to 1.67) were studied for the first time in different samples and populations of this species. Individuals with the predominant numbers of B chromosome (as a rule, zero to two) were revealed in both groups of animals (with stable and mosaic karyotypes), but the frequency was different in geographical regions. The spectra of B chromosome variability were wider in mosaics (zero to seven) compared to animals with stable karyotypes (zero to four). The importance of this for species of the high frequency of individuals with B chromosomes and with mosaicism has been discussed. The adaptive role of the low number of B chromosomes (one to two), as well as the imbalance of the B chromosome system for the species as a whole is assumed.     

Relationship between group G chromosomes, especially chromosome 21, and the sensitivity of human cells to Coxsackie B viruses]

The R-method of differential chromosome staining by length was applied to comparative karyological studies on the culture of J 96 human cells susceptible to enteroviruses, and on the J 41 cell line derived from this culture and possessing high specific resistance to Coxsackie B viruses. Karyotype of the J 41 cell line was shown to be deprived of chromosome G21 (P less than 0.0001). The number of other chromosomes varied from cell to cell, but they are constantly present in the majority of cells of both the J 96 and J 41 cell lines. A conclusion is drawn that chromosome G21 incorporates gene(s) which controls the human cells susceptibility to Coxsackie B viruses.     

The B-chromosome system of Tettigidea lateralis (Say)

Additional samples from a discrete population of the pygmy grasshopper Tettigidea lateralis, at the periphery of the species range, have shown that the frequency of the B-chromosomes has remained stable over a two year period (30-35%), and that there is not significant difference for this metric in the two sexes. The intensity of the preferential movement of the B with the X at male first meiotic division has also remained constant in time and homogenous in different individuals. Hence it is possible that this distortional effect plays a role in the equilibrium frequency of the B in the population. The B's may possess special adaptive properties under ecologically marginal conditions, since in a number of more 'central' demes they occur at much lowere frequencies (7-9%). -Unique morphological and/or behavioral variants of the standard B were encountered in addition to distinct cases of spontaneous fragmentation of A elements. The meiotic behavior and chromatic expression of these centric fragments provide evidence on the possible origin and evolution of supernumeraries. A modified. Giemsa staining technique has been used to identify regions of centromeric (C-) hererochromatin in mitotic and meiotic chromosomes. The C-banding pattern of the X and the allocyclically similar B is compared. It suggested that the B may have originated from the X by deletion of centromeric heterochromatin. This may have affected the centromere "strength" of the nascent B leading to its preferential movement with the X at anaphase I.     

The occurrence of different Bs in Cestrum intermedium and C. strigilatum (Solanaceae) evidenced by chromosome banding

In this study, we examine the morphology, mitotic stability, meiotic behavior and the composition of heterochromatin of B chromosomes in Cestrum intermedium and C. strigilatum. The results showed that B chromosome number shows intraindividual variation in the root meristem, which seems to lead to a slight rate of B elimination in this somatic tissue. B chromosomes in both species were similar in size and shape, but differed with regard to the type, size and distribution of heterochromatin. Possible evolutionary pathways for B chromosome origin in Cestrum are discussed.     

A microsatellite sequence from the rice blast fungus (Magnaporthe grisea) distinguishes between the centromeres of Hordeum vulgare and H. bulbosum in hybrid plants.

A TC/AG-repeat microsatellite sequence derived from the rice blast fungus (Magnaporthe grisea) hybridized to all of the centromeres of Hordeum vulgare chromosomes, but hybridized faintly or not at all to the chromosomes of Hordeum bulbosum. Using this H. vulgare centromere-specific probe, the chromosomes of four F1 hybrids between H. vulgare and H. bulbosum were analyzed. The chromosome constitution in the root tips of the hybrids was mosaic, i.e., 7 (7v, H. vulgare) and 14 (7v + 7b H. bulbosum), or 14 (7v + 7b) and 27 (14v + 13b), or 7 (7v), 14 (7v + 7b), and 27 (14v + 13b). The 27-chromosome tetraploid hybrid cells were revealed to have the NOR (nucleolus organizer region) bearing chromosome of H. bulbosum in a hemizygous state, which might indicate some role for this chromosome in the chromosome instability of the hybrid condition. The chromosomal distribution showed that the chromosomes of H. vulgare were concentric and chromosomes of H. bulbosum were peripheral in the mitotic squash. This non-random chromosome distribution and the centromere-specific repeated DNA differences in the two species were discussed in relation to H. bulbosum chromosome elimination. Meiotic chromosome analyses revealed a high frequency of homoeologous chromosome pairing in early prophase. However, this chromosome pairing did not persist until later meiotic stages and many univalents and chromosome fragments resulted. These were revealed to be H. bulbosum by fluorescence in situ hybridization (FISH) analysis with the H. vulgare centromere-specific probe. Because the chromosome segregation of H. vulgare and H. bulbosum chromosomes at anaphase I of meiosis was random, the possibility for obtaining chromosome substitution lines in diploid barley from the diploid hybrid was discussed.     

B chromosomes in Stylidium crossocephalum (Angiospermae:Stylidiaceae)

Populations of Stylidium crossocephalum contain two common types of B chromosomes, macro B chromosomes and micro B chromosomes. The macro B chromosomes are telocentric, slightly smaller than the smallest A chromosomes and mitotically unstable. They have so far been found associated with 6 of the 16 stable genomes known in S. crossocephalum, occurring in populations covering a substantial portion of the species range. Micro B chromosomes are about one third the length of the smallest A chromosome, acrocentric and show some mitotic instability. They occur associated with 3 stable genomes in populations found in the more medial regions of the species range. Both types of B chromosomes generally show regular behaviour during meiosis, although when two or more are present their pairing efficiency is reduced when compared to the A chromosomes. In addition a single very large mega chromosome was found in a single cell of one heterokaryotypic plant. Its origin although conjectural at this stage may be of relevance in understanding the origin of macro and micro B chromosomes in this species.     

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.     

18-26S rDNA在4种重楼属植物中的定位

为探讨rDNA在重楼属Paris L.中的分布规律,利用荧光原位杂交（FISH）对4种重楼属植物 的18-26S rDNA进行了定位。所有植物均为二倍体,基因组由A、B、C、D和 E5条染色体构成。（1）滇重楼P.polyphylla var.yunnanensis:2n=10=6m+4t,C和D染色体的 短臂上各有1个18-26S rDNA位点;（2）长柱重楼P.forrestii:2n=10=6m+4t,B染色体的长臂 、C和D染色体的短臂上各有1个位点;（3）五指莲P.axialis:2n=10=6m（2sat）+4t（2sat） +1-2B,C和D染色体的短臂上各有1个位点;在有1个B染色体的细胞中,B染色体没有信号点, 而有2个B染色体的细胞中,只有1个B染色体上有信号点,表明B染色体上有基因存在且其分裂 不均等;（4）大理重楼P.daliensis:2n=10=4m+2sm+2st+2t,C染色体的短臂上有1个位点。1 8-26S rDNA位点不仅出现在染色体的次缢痕上,也出现在非次缢痕位点。另外,4个种中C染 色体短臂末端均有18-26S rDNA。