Cytological, genetic and evolutionary functions of chiasmata based on chiasma graph analysis.

The nature of the chiasma as a cytological parameter for analysing cross-over was reexamined quantitatively by an improved chiasma graph method. It was reconfirmed in Mus platythrix (n =13) that interstitial chiasmata at diakinesis are distributed randomly and almost uniformly along bivalents except for the centromere and telomere regions. The size of these chiasma blank regions was consistently 0.8% of the total length of haploid autosomes in all chromosomes. There was a minimum value of chiasma interference distance between two adjacent chiasmata, which was constantly 1.8% in all chromosomes. The chiasma frequency at diakinesis was 20.1+/-2. 0 by the conventional method including terminal chiasmata. However, the primed in situ labeling technique revealed that terminal chiasmata were mostly telomere-telomere associations. From these data and also from recent molecular data we concluded that the terminal chiasma is cytologically functional for ensuring the normal disjunction of bivalents at anaphase I, but genetically non-functional for shuffling genes. The chiasma frequency excluding terminal chiasmata was 14.6+/-1.8. Reexamination of the chiasma frequency of 106 animal species revealed that the chiasma frequency increased linearly in proportion to the haploid chromosome number in spite of remarkable difference in their genome size. The increase in chiasma frequency would be evolution-adaptive, because gene shuffling is expected to be accelerated in species with high chromosome numbers.     

Data and theory for a revised chiasma map of man

Summary Chiasma maps appropriate to chiasma conservation and terminalization are derived from new data on chiasma distributions and high-resolution banding. Here detailed data for arms with and without a terminal chiasma and improved estimates of mapping parameters are given. Utility of chiasma maps is limited by uncertainty about the nature and extent of chiasma movement. These results are being integrated with genetic data and physical assignments.This work was supported by grant GM 17173 from the U.S. National Institutes of Health. We are grateful to M. Hulten for unpublished data     

Cyclic variation of chiasma frequency and distribution in Podarcis sicula (Reptilia: Lacertidae)

The seasonal variations of chiasma frequency and distribution have been studied in the lizard: Podareis sicula. In this species, as in Phyllodactylus (King & Hayman, Chromosoma 69: 131–154, 1978), chiasma frequencies vary following a definite annual cycle, and clearly different trends are shown by interstitial and terminal chiasmata.A comparison between these seasonal chiasma frequency variations and those of environmental temperature shows the existence of a clear correlation between these two parameters. However, this correlation is different in the two types of chiasmata, and may be different within the same type of chiasma depending on the period of the year.A more significant correlation is observed between chiasma cycles and annual variations of the haematic levels of sexual steroid hormones. In particular we observe a highly significant correlation between interstitial chiasma frequencies and testosterone concentration. A less precise correlation between terminal chiasma frequencies and estradiol concentration is also observed.In Podarcis, as in Phyllodactylus, the sperm that will be used for fertilization derive from the spermatocytes showing the highest rate of interstitial chiasmata. This supports the hypothesis that the cyclic variations in interstitial chiasma frequencies represent a mechanism to ensure an adequate level of variability in a given population. The above mentioned correlation between chiasma frequencies and steroia hormone concentrations suggests that the seasonal chiasma cycles are controlled by the same environmental and hormonal factors regulating the spermatogenetic cycle.     

Son-sire-regression based heritability estimates of chiasma frequency, using T70H mouse translocation heterozygotes, and the relation between univalence, chiasma frequency and sperm production.

T(1;13)70H/+ translocation heretozygous mice were used for assessing heritability values for chiasma frequencies and the epididymal sperm count. The chiasma frequency estimates were based on 15 son-sire pairs, the translocation heterozygotes being maintained in a Swiss random-bred genetic background. The chiasma frequencies were scored separately for the T70H/+ derived multivalent, specific pairing segments within the multivalent and the remaining bivalents. Chiasma counts within these specified parts of the genome were positively correlated. The heritability estimates, significantly greater than zero, ranged from 0.78-0.98, depending on the chromosome segments included. These results indicate a strong genetic control on a cellular basis for the formation of chiasmata in the mouse. Despite significantly positive correlations and regressions between the various chiasma frequencies and the sperm count (for which 29 pairs of observations were available), no significant heritability estimate for the sperm count was obtained. The relation between the chiasma frequency and the sperm count was weakest when the chiasma count was confined to a region of the translocation-caused multivalent in which the absence of a chiasma almost always resulted in the production of an univalent. This indicates that in the translocation heterozygotes used, the overall chiasma frequency has a greater predictive value for the sperm count than autosomal univalence alone.     

Cytology of inbreds and f 1 hybrids of pearl millet

Summary The meiotic behaviour of chromosomes was studied in four inbred lines and their F ₁ hybrids of P. typhoides. The inbred lines showed a decrease in mean chiasma frequency when compared with the population plants, but differed from one another in their mean chiasma frequencies. Together with the decrease in mean chiasma frequency the inbreds showed variation in mean chiasma frequencies. The inbred lines showed a number of meiotic abnormalities such as extra chromosomes, extra fragments, desynapsis, persistent nucleoli and differential condensation of chromosomes. The F ₁ hybrids of these inbreds exhibited heterosis for chiasma frequency. All the F ₁'s had mean chiasma frequencies higher than the means of the respective participating parents. The F ₁'s, however, differed in the degree of heterosis exhibited. In the F ₁ hybrids, the variation in mean chiasma frequency, both between plants and between PMC's within plants, was significantly lower than that of the inbred lines. The effect of environment was studied in the inbred lines and their F ₁ hybrids. The mean chiasma frequencies of the inbred lines were significantly lower, and the variation in mean chiasma frequencies was greater, in the stress season. The mean chiasma frequencies of F ₁'s did not show any significant differences between the two seasons. The F ₁'s exhibited less variation in mean chiasma frequency than the inbred lines, showing that F ₁'s were developmentally more stable. The F ₁'s did not show any meiotic abnormalities in either season.     

Relationships between frequency,localization and errors in chiasma formation in desynaptic rye

Four inbred lines of rye (Secale cereale) and the F₁ and F₂ from the cross between two of them have been studied. The results indicate that the genotypes used show variation in chiasma frequency, chiasma error frequency and chiasma localization. Significant correlations between these characters have been found: as chiasma frequency decreases both chiasma error frequency and distal localization increase. These correlations lead us to the assumption that these anomalies are in fact secondary effects of the failure of some preconditions for exchange. It is suggested that one such exchange precondition may be effective pairing.     

The control of chiasma distribution in the locust,Schistocerca gregaria (Forskål)

Chiasma distribution at diplotene in Schistocerca gregaria males can be taken to indicate the positions at which crossing over occurred prior to diplotene since chiasma terminalisation is entirely absent. Analysis of chiasma frequency and position leads to a model for the mechanism controlling distribution which has three main components. — i) The bivalents vary in length between cells due to unknown factors and increase in bivalent length leads to an increase in chiasma frequency. — ii) Within bivalents chiasma initiation is sequential from telomere to centromere with the first chiasma usually forming close to the telomere. — iii) Interference operates with the same polarity and determines a distance within which crossing over is precluded.     

The effect of B chromosome number on chiasma frequency within and between individuals of Gibasis linearis (Commelinaceae)

Meiotic analysis of 21 plants from a single population of Gibasis linearis which contained from 0 to 6 apparently identical B chromosomes showed that the mean chiasma frequencies were significantly higher with increasing numbers of Bs. It was also found that those meiotic cells of a 5B plant which contained fewer than five B chromosomes showed a marked fall in chiasma frequency, demonstrating that the influence of B chromosomes on chiasma formation in A chromosomes acts at a cellular rather than a whole-anther level.     

Meiotic chromosomes of green frogs (Rana esculenta complex) of the Ukraine territory

In this work meiotic chromosomes of R. ridibunda, R. lessonae and their hybrid form R. esculenta of the Ukraine territory are described for the first time. These chromosomes are connected in diakinesis more often by two chiasma, rarely by one or three chiasma in 13 bivalents. Bivalents with one chiasma in R. ridibunda are typical only for large bivalents, in R. lessonae only for small ones. Three chiasma in parental species are typical only for small bivalents. In the hybrid form R. esculenta chromosomes with two, one and three chiasma are typical both for large bivalents, and for small ones. In the hybrid form (R. esculenta) chiasma frequency noticeably decreases, comparatively with parental species that, possibly, specifies the aberration of normal meiosis realization. The chiasma frequencies of the hybrid form of the eastern and the southern parts of Ukraine are almost the same, but the types of chromosomes are different in such regions. In the eastern region chromosomes of the hybrid form are represented by two or one chiasma, in the southern region by two, one or three chiasma.     

Influence of B-chromosomes on meiosis in pearl millet

B-chromosome behaviour and the effects of B's on the endophenotype were studied in the third back-cross progeny of a cross between non-B and B-carrying parents ofPennisetum typhoides Stapf et Hubb. In the experimental material a regular increase in B-chromosome chiasma frequency and an increase in the variation of mean chiasma frequency with increased number of B's was observed. When four or more B-chromosomes were present quadrivalents occurred more frequently. In these respects the experimental material differed from the B-carrying parent. B's had no effect on the mean chiasma frequency of A-chromosomes when present in numbers of up to and including four but when present in numbers of more than four had a depressing effect. The variation of the mean chiasma frequency of the A-chromosomes increased with increasing number of B's. No correlation was observed between A-chromosome chiasma frequencies and B-chromosome chiasma frequencies. In the experimental material B's when present in larger numbers i.e. more than four had deleterious effects on A-chromosome behaviour and on fertility. In the effects of B's on the endophenotypic characters the experimental material differed from the B-carrying parent. It is suggested that the behaviour and effects of B's on the endophenotypic characters are the result of interaction between the A-chromosome genotype and the B-chromosomes.     

The chiasma-inducing pheromone of locusts

To the two quantitative criteria for phase transformation of locusts, viz. nymphal colour and adult morphometric ratios, the change in chiasma frequencies during meiosis in the male can now be added: gregarization or swarming induces an increase in chiasma formation. The atmosphere around crowded locusts contains a pheromone which is absorbed and causes a reactive haemolymph in locust hoppers. This haemolymph may be injected into solitarious hoppers or nymphs to induce increased chiasma formation. Certain solvents like risella oil and dimethyl sulphoxide will extract the pheromone from such an atmosphere, and bio-assays with these extracts have been demonstrated to be chiasma-inducing. Such extracts are, however, not chiasma-inducing in the albino mutant, but the haemolymph from crowded normal-coloured hoppers is reactive in the albino hopper. In addition the albino mutant is solitaria-like in both morphometric ratios and chiasma frequencies. These data indicate a relationship between the melanization cycle and chiasma induction: the previously postulated melanin-inducing pheromone and this chiasma-inducing pheromone are probably identical. On the other hand, this pheromone of nymphs and the sex-maturation pheromone of adults are not identical, although the latter may be a modified form of the other. The effect of the nymphal pheromone on adult morphometric ratios is not clear although some correlation has been shown to exist between raised chiasma frequencies in treated solitaries and advances towards gregaria ratios. It may be that in this pheromone we have, what may be called, a gregarizing principle.     

Age trends in human chiasma frequencies and recombination fractions. I. Chiasma frequencies.

Chiasma frequency data on 183 males were subjected to an analysis of covariance. There appeared to be little or no linear trend in chiasma frequency with age. This conclusion was supported by a detailed analysis of chiasma frequencies for each autosome from 21 males. There were, however, significant differences among investigators in reported mean chiasma frequencies.     

Formation of chiasmata in the synchronous meiotic cycle of Lilium longiflorum

The results of treatment of meiotic cells of Lilium longiflorum by cycloheximide at the time of chiasma initiation and formation suggest that in the sequential phases of nuclear development, complete chiasma suppression resulting in achiasmate cells is attained prior to a quantitative reduction of chiasma frequency. Reduction of chiasma frequency and complete suppression are believed to be based on two different mechanisms.     

The control of chiasma distribution in rye

The chiasma conditions have been extensively analysed in two contrasting rye genotypes, one showing a normal and regular pattern of chiasma distribution and the other showing a highly abnormal and asymmetrical pattern of chiasma distribution. The analyses show that the pattern of chiasma distribution in the abnormal genotype conforms to the statistical expectations of randomness, and this is interpreted as being due to a breakdown of the processes which govern the distribution of chiasmata in normal rye genotypes. On the basis of these findings it is proposed that two independent and fundamentally different control systems are involved in the maintenance of efficient chiasma conditions in rye. One of these controls simply gives competence for chiasma formation, the other control system is evidently concerned with regulating the distribution of chiasmata. Analysis of two trisomic genotypes reveals that the conclusions relating to large samples of bivalents are also applicable to particular identifiable chromosomes. The results of brceding tests involving the two contrasting genotypes show that the control of chiasma distribution in rye has a complex genetic basis.This investigation was started while the author was in receipt of an Agricultural Research Council studentship at the Agricultural Botany Department, University College of Wales, Aberystwyth.     

Asynapsis in Lolium perenne

Eighteen plants displaying varying degrees of asynapsis ranging from weak to very strong were found among four out of six populations of Lolium perenne L. (2n=14) which had been subjected to three cycles of directional phenotypic selection for productivity of green material. No plants were found displaying univalents in the original generation but the incidence increased with cycles of selection, indicating the genetic control and differential distribution of asynaptic genes among these populations. — The analysis of univalents and chiasma frequency of pollen mother cells (PMC) of six partially asynaptic plants chosen for detailed study revealed that univalents occurred throughout all PMC chiasma classes irrespective of chiasma frequency, but the higher the chiasma frequency of any PMC the less the likelihood of univalents occurring. The relationship between chiasma frequency and univalent frequency per PMC per plant was negative. — Mean chiasma frequency per bivalent increased for the asynaptic cells in comparison with the normal in both the weak and medium asynaptic groups which was explained by the availability of additional chiasmata for redistribution.     

The effect of Actinomycin-D on chiasma frequency in Vicia faba

The effect of Actinomycin-D was studied on chiasma frequency in Vicia faba (var. Weibull's Akerabona). A significant decrease in chiasma frequency over control was observed in all cases irrespective of the time of fixation and chemical concentration. However, the maximum decrease was found in the material fixed after a recovery period of 24 hours. The decrease in chiasma frequency showed a linear relationship with time of recovery. Besides reduction in the chiasma frequency, cells showing complete failure of homologous pairing were also observed. These findings are discussed in the light of actinomycin-D action.     

Chiasma syndrome in acromegalic patients--correlation of neuroradiologic and neuroophthalmologic findings

The study evaluated neuroophthalmologic and computerized tomography (CT) findings in 100 patients with somatotrophic adenoma and clinical picture of acromegaly, who underwent transsphenoidal adenomectomy. Prior to the surgery, visual field was normal in 77 patients. The diameter of adenoma in these patients ranged from 8 to 30 mm on CT, and the average value was 13.5 mm. Various kinds of visual field disturbances were present in 23 patients. The diameter of their adenomas ranged between 18 to 35 mm, with the average of 24.7 mm. Compared to visual field defects, CT findings of suprasellar adenoma extension were better correlated with chiasma syndrome (p < 0.001). All patients with suprasellar mass greater than 10 mm had chiasma syndrome. Degenerative adenoma changes (hemorrhagic necrosis), which precipitate abrupt increase in size of the tumor, were more frequently seen in patients with chiasma syndrome. The incidence of chiasma syndrome directly correlates with the degree of suprasellar extension of the tumor.     

Chiasmata and variability in Lolium and Festuca populations

There are significant differences in mean pollen mother cell chiasma frequencies between populations within Lolium perenne, L. multiflorum and Festuca pratensis. The differences are genotypically controlled. With low chiasma frequencies the chiasmata are distally located. With increasing chiasma frequency the frequency of chiasmata in interstitial segments increases. Shorter lived populations have higher chiasma frequencies than the more perennial. — The higher the chiasma frequency of a population the lower the phenotypic and genetic variance for characters under polygenic control, such as flowering time, and the less effective also is the response to selection for such characters. These observations are interpreted on the premise that high chiasma frequencies are instrumental in the breaking up of supergene sequences in interstitial chromosome segments.     

Chiasma frequency,distribution and interference maps of mouse autosomes

Chiasma frequencies were analysed and chiasma positions measured in diakinesis/metaphase I autosomal bivalents from oocytes and spermatocytes of F₁ hybrid C3H/HeH×101/H mice. Twenty chromosome size ranks, including the presumptive X bivalent, could be distinguished in oocytes, and nineteen autosomal ranks plus the XY pair spermatocytes. Overall, mean cell chiasma frequencies of the two sexes did not differ significantly once the contribution of the presumptive X bivalent and the XY pair were taken into account. Sex related differences in chiasma distribution patterns were evident, however. In monochiasmate bivalents, the chiasma was most commonly located interstitially in oocytes while in spermatocytes it could be either interstitial or distal. In dichiasmate bivalents, the chiasmata tended to be more centrally located in oocytes than in spermatocytes. Minimum inter-chiasma distances did not appear to show any great variation in chromosome pairs of different sizes, however, mean inter-chiasma distances did increase with the bivalent length. The minimum-inter chiasma distance data suggest that chiasma interference is complete over a chromosomal segment equating to approximately 60 Mb. Measurement of the positions of chiasmata along chromosome arms open up the possibility of producing chiasma-based genetic maps for all the autosomes of the mouse.     

Chiasma-based genetic map of the mouse X chromosome

The X chromosome pair was identified in diakinesis/metaphase I stage mouse oocytes using a repeat sequence DNA probe and fluorescence in situ hybridisation. Chiasma positions along the X bivalent were measured in 57 oocytes from 4 females. Overall, our observations showed that while there were no obvious hotspots for chiasma formation along the X chromosome, there was a tendency to favour the distal end. Minimum inter-chiasma distances were substantial indicating the occurrence of strong genetic interference. Estimates of both genetic distances and recombination fractions for any interval along the chromosome can be calculated from the chiasma data. The average chiasma frequency for the X bivalent was 1.37 giving an estimated total genetic map length of 68.5 cM. In general, the pattern of chiasma distribution along the X chromosome resembled that anticipated from recombination distances in published consensus linkage maps. There were, however, some intriguing differences between the two approaches. The reason for these discrepancies are unknown but may be related to lack of precision in cytogenetic mapping of loci, inter-strain and/or interspecies differences in the genetic controls over the distribution of crossover events. One advantage of the chiasma analysis approach is its suitability for investigating these problems.