Cytogenetic studies on <Emphasis Type="Italic">Metasequoia glyptostroboides</Emphasis>, a living fossil species

The chromosome morphology and meiotic pairing behavior in the pollen mother cells (PMCs) of Metasequoia glyptostroboides were investigated. The results showed that: (1) The chromosome number of the PMCs was 2n=22. (2) The PMCs developed in the successive manner, and the nucleoids in the dynamic development were similar to those of the other gymnosperms. (3) At prophase, most of the chromosomes were unable to be identified distinctively because the chromosomes were long and tangled together. The chromosome segments were paired non-synchronously. At pachytene, the interstitial or terminal regions of some bivalents did not form synapsis and the paired chromosomes showed difference in sizes, indicating that there were structure differences between the homologous chromosomes. (4) At diakinesis, the ring bivalents showed complicated configurations due to the differences in location and number of chiasmata. In addition, there were cross-linked bivalents. (5) At metaphase I, the chromosome configuration of each cell was 8.2II ⁰ + 1.1II + 1.3II ⁺ + 0.8I. Most of the chromosomes were ring bivalents, but some were cross-linked bivalents, rod bivalents, or univalents. (6) 15\% PMCs at anaphase I and 22\% PMCs at anaphase II presented chromosome bridges, chromosome fragments, micronuclei, and lagging chromosomes. Twenty seven percent microspores finally moved into one to three micronuclei. Twenty five percent pollens were abortive. The results indicated that the observed individual of M. glyptostroboideswas probably a parpcentric inversion heterozygote, and there were structural and behavioral differences between the homologous chromosomes. The chromosomal aberration of M. glyptostroboidesmay play an important role in the evolution of this relict species, which is known as a living fossil. Further evidence is needed to test whether the differences between homologous chromosomes were due to hybridization.     

The induction of orientational instability and bivalent interlocking at meiosis

The administration of 40° C heat-treatments was found to induce bivalent orientational instability and interlocking at male meiosis in the locust Locusta migratoria. Only the longest members of the complement showed orientational instability and these usually possessed single distally sited chiasmata, with near-maximal intercentromeric distances. An effect on the stability of spindle fibre microtubule association, or attachment to the chromosome, is considered to be a possible explanation of the behaviour found. Bipolar orientation was generally achieved prior to anaphase I so that chromosome segregation was usually normal. Diamphitelic bivalents provided the most common exception to this rule. They sometimes lagged at anaphase, with the separation of half-bivalents and the production of structures indistinguishable from lagging univalents. The bivalent interlocking also involved the longest members of the complement. Most combinations of rod/rod, rod/ring and ring/ring types of interlocking were found. Usually only two bivalents were interlocked in any one cell, although occasionally three were found interlocked. All types appeared to involve an effect on the regulation of chromosome pairing, although at least one of the cells found showed interlocking caused by the metaphase orientational instability. In most cells, interlocked bivalents showed stable orientation and this usually involved the unipolar orientation of each bivalent's two centromeres. Such configurations provide concrete support for the importance of physical tension in the maintenance of metaphase orientational stability. They lead to double non-disjunction at anaphase I. Interlocked bivalents showed normal congression to a mid-equatorial position with no tendency for the re-adjustment of arm ratios to equalise centromere distances from the poles. This behaviour is discussed in relation to spindle fibre dynamics and it is concluded that no hypothesis of congression currently available can satisfactorily explain all that we know of the behaviour of univalents, bivalents, multivalents and interlocked bivalents.     

Meiotic chromosome structure. Kinetochores and chromatid cores in standard and B chromosomes of Arcyptera fusca (Orthoptera) revealed by silver staining.

The behaviour of two chromosome structures in silver-stained chromosomes was analyzed through the first meiotic division in spermatocytes of the acridoid species Arcyptera fusca. Results showed that at diakinesis kinetochores and chromatid cores are individualized while they associate in bivalents of metaphase I; only kinetochores and distal core spots associate in the sex chromosome. Metaphase I is characterized by morphological and localization changes of both kinetochores and cores which define the onset of anaphase I. These changes analyzed in both autosomes and in the sex chromosome allow us to distinguish among three different substages in metaphase I spermatocytes. B chromosomes may be present as univalents, bivalents, or trivalents. Metaphase I B univalents are characterized by separated cores except at their distal ends and individualized and flat sister kinetochores. At anaphase I sister kinetochores of lagging B chromatids remain connected through a silver-stained strand. The behaviour of cores and kinetochores of B bivalents is identical with that found in the autosomal bivalents. The differences in the morphology of kinetochores of every chromosome shown by B trivalents at metaphase I may be related to the balanced forces acting on the multivalent. The results show dramatic changes in chromosome organization of bivalents during metaphase I. These changes suggest that chromatid cores are not involved in the maintenance of bivalents. Moreover, the changes in morphology of kinetochores are independent of the stage of meiosis but correlate with the kind of division (amphitelic-syntelic) that chromosomes undergo.     

Segregation of the amphitelically attached univalent X chromosome in the spittlebug <Emphasis Type="Italic">Philaenus spumarius</Emphasis>

In meiosis I, homologous chromosomes combine to form bivalents, which align on the metaphase plate. Homologous chromosomes then separate in anaphase I. Univalent sex chromosomes, on the other hand, are unable to segregate in the same way as homologous chromosomes of bivalents due to their lack of a homologous pairing partner in meiosis I. Here, we studied univalent segregation in a Hemipteran insect: the spittlebug Philaenus spumarius. We determined the chromosome number and sex determination mechanism in our population of P. spumarius and showed that, in male meiosis I, there is a univalent X chromosome. We discovered that the univalent X chromosome in primary spermatocytes forms an amphitelic attachment to the spindle and aligns on the metaphase plate with the autosomes. Interestingly, the X chromosome remains at spindle midzone long after the autosomes have separated. In late anaphase I, the X chromosome initiates movement towards one spindle pole. This movement appears to be correlated with a loss of microtubule connections between the kinetochore of one chromatid and its associated spindle pole.     

THE QUESTION OF POST-REDUCTION IN SPHAGNUM

The 19 spatially distinct chromosomal units at first meiotic metaphase in sporophytically diploid species of Sphagnum have usually been considered to be bivalents, but one investigator (Sorsa, 1956) has interpreted them as chromosomes from dissociated bivalents and meiosis as post-reductional. The present studies on diploid S. squarrosum (Pers.) Crome establish the chromosome number on the basis of the following evidence: there are in addition to m-chromosomes, 19 pairs of chromosomes in early prophase, 19 bivalents at diakinesis, 19 chromosomes in each of the two sets at second metaphase, 19 daughter chromosomes in each of the four sets at late second anaphase, and 19 chromosomes in gametophytic mitoses. The 19 bodies at first meiotic metaphase in diploid species are true bivalents in loose secondary association, which has led to their erroneous interpretation as chromosomes of dissociated bivalents. The gametic chromosome number in sporophytically diploid Sphagnum is therefore, without doubt, n = 19, and this evidence negates the claim for post-reduction in Sphagnum.     

Cytological studies on meiosis and male gametophyte development in autotetraploid cucumber

With improved staining and chromosome preparation techniques, meiosis of pollen mother cells (PMCs) and male gametophyte development in autotetraploid cucumber (Cucumis sativus L.) was studied to understand the correlation between chromosomes behaviour and fertility. Various chromosome configurations, e.g. multivalent, quadrivalents, trivalents, bivalents and univalents were observed in most PMCs at metaphase I. Lagging chromosomes were frequently observed at anaphase in both meiotic divisions. In addition, chromosomes segregations were not synchronous and equal in some PMCs during anaphase II and telophase II. Dyads, triads, tetrads with micronuclei and polyads were observed at tetrad stage, and the frequencies of normal tetrad with four microcytes were only 55.4 %. The frequency of abnormal behaviour in each stage of meiosis was counted, and the average value was 37.2 %. The normal meiotic process could be accomplished to form the microspore tetrads via simultaneous cytokinesis. Most microspores could develop into fertile gametophytes with 2 cells and 3 germ pores through the following stages: single-nucleus early stage, single-nucleus late stage and 2-celled stage. The frequency of abnormalities was low during the process of male gametophyte development. The germination rate of pollen grains was 46.9 %. These results suggested that abnormal meiosis in PMCs was the reason for low pollen fertility in the autotetraploid cucumber.     

Meiosis in Drosophila melanogaster

Individual bivalents or chromosomes have been identified in Drosophila melanogaster spermatocytes at metaphase I, anaphase I, metaphase II and anaphase II in electron micrographs of serial sections. Identification was based on a combination of chromosome volume analysis, bivalent topology, and kinetochore position. — Kinetochore microtubule numbers have been obtained for the identified chromosomes at all four meiotic stages. Average numbers in D. melanogaster are relatively low compared to reported numbers of other higher eukaryotes. There are no differences in kinetochore microtubule numbers within a stage despite a large (approximately tenfold) difference in chromosome volume between the largest and the smallest chromosome. A comparison between the two meiotic metaphases (metaphase I and metaphase II) reveals that metaphase I kinetochores possess twice as many microtubules as metaphase II kinetochores. — Other microtubules in addition to those that end on or penetrate the kinetochore are found in the vicinity of the kinetochore. These microtubules penetrate the chromosome rather than the kinetochore proper and are more numerous at metaphase I than at the other division stages.     

Meiotic studies in Acanonicus hahni (Stål) (Coreidae,Heteroptera) I. Behaviour of univalents in desynaptic individuals

Male meiosis was studied in a population of Acanonicus hahni (Stål), and nine of the sixteen individuals analyzed showed desynapsis. The frequency of univalents varied from one to seven percent in eight of them, while in the ninth the percentage of cells with univalents was higher (12%). The univalents auto-orientate at metaphase I in the center of the ring formed by autosomal bivalents and divide equationally at anaphase I; at metaphase II they show touch-and-go pairing, and lie in the center of the ring of autosomes.A desynaptic origin of the univalents is proposed, and the arrangement of the chromosomes in the first and second metaphase plate in the normal and desynaptic individuals is compared and discussed. The meiotic characteristics of these desynaptic individuals are also compared with those described in other insects with holocentric and monocentric chromosomes. It is suggested that any achiasmatic chromosome, whether a univalent, m or sex chromosome, will induce the formation of a ring and with some or all of them lying in its centre.     

Meiotic behavior of an unequal bivalent in the grasshopper Calliptamus palaestinensis Bdhr.

Summary Unequal bivalents were found in two of four populations of the short horned grasshopper, Calliptamus palaestinensis bdhr. sampled in Israel.The inequality of the homologues was due to an extra segment which was heterochromatic and apparently terminal. Pairing configurations at pachytene and position of chiasmata at later stages revealed however that the extra segment was interstitial, and the long member terminated in a minute segment homologous to the terminal part of its normal partner. The percentage of reductional divisions at anaphase I corresponded well with the percentage of terminal chiasmata (i.e. distal to the extra segment) observed at diakinesis.The assumption of an interstitial position of the extra segment would explain the previously puzzling examples of unequal bivalents in Orthoptera whose reductional divisions have not been readily accounted for otherwise.     

Further studies on polyploid amphibians (Ceratophrydidawe)

Odontophrynus cultripes Reinhardt and Lutken, 1862 has 22 chromosomes in its diploid complement. Spermatocyte I contained 11 ring bivalents and metaphase II exhibited 11 chromosomes. Odontophrynus americanus (Duméril and Bibron) 1882 has 44 chromosomes in somatic as well as germ cells, these can be sorted into 11 groups of homologues. Metaphase I showed varying numbers of quadrivalents and metaphase II exhibited 22 dyads. Ceratophrys dorsata Wied., 1824 has 104 chromosomes in somatic and germ cells; these 104 chromosomes comprise 8 each of 13 kinds of homologues. The spermatocyte I contained ring octovalents and other multivalents, and metaphase II 52 chromosomes. The above findings indicate that evolution by polyploidization occurred in South American frogs belonging to the family Ceratophrydidae.This work was supported by a grant (GM-14577-01) from the National Institute of General Medical Sciences U. S. Public Health Service.     

Co-segregation of sex chromosomes in the male black widow spider <Emphasis Type="Italic">Latrodectus mactans</Emphasis> (Araneae,Theridiidae)

During meiosis I, homologous chromosomes join together to form bivalents. Through trial and error, bivalents achieve stable bipolar orientations (attachments) on the spindle that eventually allow the segregation of homologous chromosomes to opposite poles. Bipolar orientations are stable through tension generated by poleward forces to opposite poles. Unipolar orientations lack tension and are stereotypically not stable. The behavior of sex chromosomes during meiosis I in the male black widow spider Latrodectus mactans (Araneae, Theridiidae) challenges the principles governing such a scenario. We found that male L. mactans has two distinct X chromosomes, X₁ and X₂. The X chromosomes join together to form a connection that is present in prometaphase I but is lost during metaphase I, before the autosomes disjoin at anaphase I. We found that both X chromosomes form stable unipolar orientations to the same pole that assure their co-segregation at anaphase I. Using micromanipulation, immunofluorescence microscopy, and electron microscopy, we studied this unusual chromosome behavior to explain how it may fit the current dogma of chromosome distribution during cell division.     

Centromere orientation,reorientation, and segregation in an interchange quadrivalent during anther development in pearl millet

Prometaphase I orientation, reorientation and anaphase I segregational behaviour of a chain-forming interchange quadrivalent involving one of the long chromosomes and the long arm of the seventh (nucleolar) chromosome was studied during anther development in pearl millet. The data obtained from 34 anthers showed that by early prometaphase I about 90% of the bivalents have attained stable bipolar orientation but about 48% of the quadrivalents are mal-oriented. There seems to be an interaction between bivalents and quadrivalents during mal-orientation and reorientation. The mal-oriented bivalents reoriented before the quadrivalents. For quadrivalent mal-orientation four types, 4/0, 3/1, 2/1/1/1 and 2/2 (adjacent 1), were distinguished in addition to the regular types, adjacent 2 and alternate. Based on their potential to reorient, the order of the mal-oriented quadrivalent types was 4/0 > 3/1 > 2/1/1; 2/2 led to anaphase I disjunction as for an adjacent 1 segregation. The data from 36 anthers at anaphase I showed alternate segregation of chromosomes in nearly 50% of pollen mother cells (PMCs) up to a developmental index of about 65. In late anthers about 35% PMCs showed alternate segregation. This suggests that the PMCs that reached metaphase I later had more adjacent 2 orientations since mal-oriented configurations delay meiotic development, and implies preferential reorientation behaviour of the maloriented quadrivalent types.     

Involvement of chromatid cohesiveness at the centromere and chromosome arms in meiotic chromosome segregation: A cytological approach

Kinetochores and chromatid cores of meiotic chromosomes of the grasshopper species Arcyptera fusca and Eyprepocnemis plorans were differentially silver stained to analyse the possible involvement of both structures in chromatid cohesiveness and meiotic chromosome segregation. Special attention was paid to the behaviour of these structures in the univalent sex chromosome, and in B univalents with different orientations during the first meiotic division. It was observed that while sister chromatid of univalents are associated at metaphase I, chromatid cores are individualised independently of their orientation. We think that cohesive proteins on the inner surface of sister chromatids, and not the chromatid cores, are involved in the chromatid cohesiveness that maintains associated sister chromatids of bivalents and univalents until anaphase I. At anaphase I sister chromatids of amphitelically oriented B univalents or spontaneous autosomal univalents separate but do not reach the poles because they remain connected at the centromere by a long strand which can be visualized by silver staining, that joins stretched sister kinetochores. This strand is normally observed between sister kinetochores of half-bivalents at metaphase II and early anaphase II. We suggest that certain centromere proteins that form the silver-stainable strand assure chromosome integrity until metaphase II. These cohesive centromere proteins would be released or modified during anaphase II to allow normal chromatid segregation. Failure of this process during the first meiotic division could lead to the lagging of amphitelically oriented univalents. Based on our results we propose a model of meiotic chromosome segregation. During mitosis the cohesive proteins located at the centromere and chromosome arms are released during the same cellular division. During meiosis those proteins must be sequentially inactivated, i.e. those situated on the inner surface of the chromatids must be eliminated during the first meiotic division while those located at the centromere must be released during the second meiotic division.by D.P. Bazett-Jones     

Identification of complexes in a spontaneous triploid Rhoeo spathacea

A ring-of-12 chromosomes at meiosis is characteristic of diploid Rhoeo. Each arm has been assigned a letter in accordance with the segmental interchange theory. Adjacent distribution at anaphase I results in nonviable spores while alternate distribution results in only two types of spores, both viable. Each of these two types has six chromosomes which are collectively either an or a complex. The chromosome complement of a diploid contains one of each. A theoretical diakinesis configuration in the spontaneous triploid Rhoeo is a ring with six bivalents alternating with six univalents. Among the twelve connecting positions, Position D is diagnostic in the triploid. If the complex is in duplicate, two short arms and a long arm are connected at Position D, and Univalent cD is attached to two bivalents by their short arms. In contrast, if the complex is in duplicate, two long arms and a short arm are connected at Position D, and Univalent Dd is attached to two bivalents by their long arms. Squashed preparations of PMC stained with acetocarmine were used. Among a larger number of triploid metaphase I cells studied, 53 had identifiable chromosomes. In four of the 53, all 18 chromosomes were identified. Chiasma failures in these four PMC were distributed at random among the 12 positions, and at random relative to arm length. The unique features predicted in the presence of an extra complex were observed. Root tip karyotypes had only four (rather than five) large metacentrics. It is concluded that the chromosome complement of the triploid consists of two complexes and one complex. Implications for the balanced lethal mechanism are discussed.This paper represents part of a dissertation submitted in partial fulfillment of the requirements for a Ph. D. degree in genetics at The Ohio State University, Columbus, Ohio, USA.     

Chromosome systems in the eriococcidae (Coccoidea Homoptera)

Spermatogenesis is described in two eriococcid species and the observations are compared to those previously reported. In Gossyparia spuria the diploid chromosome number is 28 in both males and females. In the female all the chromosomes are euchromatic. In most male tissues 14 of the chromosomes are euchromatic (E) and 14 are heterochromatic (H). Prior to the first meiotic division in males the number of H chromosomes was reduced. During prophase I all the cells showed 14 E chromosomes and from 1 to over 9 H chromosomes. The range of chromosome numbers in metaphase I was similar to that in prophase I. All the chromosomes divided in anaphase I, and, following differential uncoiling at interkinesis, the E and H groups of chromosomes segregated from each other at anaphase II. Only the E groups formed sperm. The presence of a variable number of H chromosomes and a haploid number of E chromosomes in spermatogenesis suggested the presence of the multiple-D variant of the Comstockiella chromosome system. In this system some of the H chromosomes become euchromatic prior to prophase I of spermatogenesis and pair with their E homologues. All the remaining H chromosomes are thus univalents, while among the E elements, some are univalents and the rest are bivalents. The observed reduction in the number of H chromosomes in the first meiotic division which was previously attributed to pairing among the H chromosomes, is now interpreted to be the result of the return of some of the H chromosomes to a euchromatic state and to their subsequent pairing with their E homologues. Spermatogenesis in Eriococcus araucariae was similar to that of G. spuria except that the reduction in the number of H chromosomes was not as extensive. The chromosome systems of the two species are compared to those of other eriococcids and the differences are briefly discussed.Supported by grant GB1585 from the National Science Foundation, Washington, D. C.     

Inversion heterozygosity and sub-chromatid exchange in Agave stricta

A plant of Agave stricta Salm. (2n=60) has a bimodal complement of 10 L, 4 M and 46 S chromosomes. It is heterozygous for a paracentric inversion which involves the middle third of the long arm of one of the L chromosomes. It produces at anaphase I bridges and fragments and also loops and fragments, both single and double. Breakage and reunion at the sub-chromatid and at the chromatid level produce side-arm bridges and bridges and fragments respectively at anaphase I. A method is given, based on chiasma frequency, which will in certain cases of inversion heterozygosity provide a reasonable estimate of the position and the length in genetic map units of an inverted segment with respect to the whole chromatid arm.     

Chromosome elimination in Paspalum subciliatum (Notata group)

 This paper reports the occurrence of chromosome elimination during microsporogenesis in a Brazilian accession of Paspalum subciliatum. The accession was tetraploid (2n=4x=40) and meiosis was normal until diakinesis, with 20 regularly distributed bivalents. Starting at metaphase I, meiosis was very peculiar. In this phase, while ten bivalents were clustered in the equatorial plate, the other ten were still dispersed in the cytoplasm. In anaphase I the chromosomes showed different abilities to migrate to the poles. While one genome reached the poles in telophase I, the laggard was in metaphase or anaphase and was engulfed by extra nuclei. In the second division, behavior was the same. Our results show clear asynchrony in cell cycle, especially in some meiotic phases. Unfortunately we cannot explain the causes of the phenomenon, but this event shows once more that chromosome elimination serves as an incompatibility barrier preventing divergent genomes from coexisting in the same cellular system. The chromosome elimination affected pollen fertility but did not impair seed viability. Received: 22 April 1998 / Revision accepted: 2 September 1998     

Meiosis in Mesostoma ehrenbergii ehrenbergii (Turbellaria,Rhabdocoela)

At metaphase I of meiosis in spermatocytes of Mesostoma ehrenbergii ehrenbergii [2n=10] three bivalents and four univalents form. The same two chromosome pairs always form the univalents. Analysis of metaphase I, anaphase I and metaphase II configurations in fixed testis material suggested that the distribution of the four univalents is not a random process but the correct segregation of one member of each pair to each pole is actively achieved before the end of metaphase I. In live preparations of testis material univalents were observed to move between the poles of metaphase I cells, eventually reaching the correct segregation. All cells observed to enter anaphase I had the correct segregation of univalents. It is proposed that the univalent movement during metaphase I is directed towards obtaining the correct segregation of univalents before the cells enter anaphase.     

Meiosis in polyhaploid Hordeum: hemizygous ineffective control of diploid-like behaviour in a hexaploid?

Meiotic chromosome behaviour was studied in the hexaploid Hordeum parodii (2n=6x=42) and in six haploids (2n=3x=21) obtained from a cross between H. parodii and H. bulbosum (2n=2x=14) whereby all bulbosum chromosomes were selectively eliminated. The alloploid nature of H. parodii was evident from the exclusive bivalent formation at the hexaploid level and the low and variable number of bivalents in its haploid derivatives. In haploids, both nonhomologous (intragenomic) and homoeologous (intergenomic) chromosomes paired at prophase. Foldbacks in single chromosomes, bivalents and trivalents were observed at prophase and metaphase I. At diakinesis, the associations involved a maximum of 20 chromosomes which decreased to 12 by metaphase I. This decrease was attributed to the failure of the non-homologous associations to persist until metaphase I. A hemizygous-ineffective control for the diploid-like behaviour of the hexaploid parodii is proposed to explain the homeologous chromosome pairing in its haploid derivatives.     

Differential behaviour of chromosomes in Scilla

Conclusion While the cause of the differential behaviour is not known we can with some confidence specify the conditions affecting its consequences. In the first place particular chromosomes respond to the abnormal conditions within the cell in different ways. InScilla it was shown that long chromosomes were more frequently retarded than short ones. A specific chromosome response was also deduced byJain inLolium, from the disproportionate preponderance of unsynchronised cells with one or two advanced bivalents. This kind of specificity may or may not be simply related to length, for example the minimum requirements for condensation may be greater for longer chromosomes. There is no evidence either way. A second condition, along with the first, would certainly appear to be the spatial relations of chromosome material within the nucleus, a factor recently discussed in general terms byDarlington (1957). On this basis the abnormal cells could be regarded as containing nuclei where co-operation was restricted, uncharacteristically, over limited distances. As suggested earlier the initial cause of this is most reasonably attributed to differences in the cytoplasm, which in normal cells permits general co-operation within nuclei, but which in abnormal cells with genetically identical nuclei, does not.