The supernumerary segment system of Stethophyma

Three species of the genus Stethophyma have been cytologically examined and all three show variation both for supernumerary heterochromatic segments and for the distribution of standard heterochromatin among the autosomes. The European species, S. grossum, for example, shows considerable interpopulation variation for standard heterochromatin while two of the populations, from Spain and Austria, show supernumerary segment polymorphism. The segments are located interstitially on the S₁₁ chromosome but occupy different positions in the different populations. — In all species, the presence of the extra heterochromatic segments increases the mean chiasma frequency. Moreover, the influence of the segments upon mean chiasma frequency is different in different populations and in different species. In the Spanish population, the increase is both intra- and interchromosomal whereas in Austria the influence of the segment is completely interchromosomal. — In the American species, S. gracile and S. lineatum, where supernumerary heterochromatic segments are carried on both S₁₀ and S₁₁ chromosomes, the effect on chiasma frequency shows a dosage relationship, an increase in the number of segments per individual being correlated with an increase in mean chiasma frequency. It is suggested that the interstitial segments found in all species have originated by direct duplication of chromosome material. By contrast the terminal segments in S. lineatum and S. gracile may be derived by translocation from a B-chromosome since such a chromosome has been found in one individual of the former species. — The variation in segment structure and the distribution of standard heterochromatin, among the European species of S. grossum suggests that these systems have evolved independently in different populations.On educational leave from the Forest Research Laboratory, Fredericton, N. B. Canada.     

Meiotic effects of supernumerary heterochromatin in Heteropternis obscurella

The endemic Australian grasshopper Heteropternis obscurella shows considerable variation in respect of both chromosome structure and chromosome behaviour. The structural differences depend upon different patterns of heterochromatin distribution as revealed by C-banding. These involve differences between populations in respect of polytypic variation in the size of paracentromeric C-bands and differences within populations in respect of polymorphisms both for terminal blocks of heterochromatin in autosomes 3 to 8 and a large proximal block of heterochromatin in autosome 7. The behavioural differences stem in part from genotypically determined variation in the chiasma distribution pattern which is markedly localised in a majority of populations but more randomly distributed in populations from the south of Western Australia. Behavioural differences also arise as secondary consequences of the presence of those heterochromatic blocks which occur as polymorphisms. The distal blocks on autosomes 5, 6, 7 and 8 lead to a redistribution of chiasmata to more proximal sites while the proximal block on 7 leads to the virtual abolition of chiasma formation in that bivalent and its replacement by a non-chiasmate mechanism of segregation. This depends upon a persistent proximal heterochromatic association between the pairing partners. The presence of distal C-blocks on bivalents 3 to 8 gives rise to persistent pseudomultiples, formed as a result of heterochromatic associations between these blocks. Such pseudomultiples involve any two or three of these six bivalents, provided they carry distal blocks, and their frequency rises dramatically in the presence of the proximal heterochromatic block on chromosome 7.     

Polymorphism involving heterochromatic segments in Metrioptera brachyptera

A complex pattern of polymorphism involving terminal heterochromatic segments on L₃ and L₄ chromosomes has been uncovered in eight populations of Metrioptera brachyptera. There are individuals in every population which carry reduced segments on one or both L₄'s. In six populations, enlarged heterochromatic segments have been encountered on the L₃ chromosomes in some individuals. The L₄ system is almost certainly stable although the frequency of L₄ karyotypes does not conform to a Hardy-Weinberg distribution in all populations. Stability of the L₃ polymorphism could not be ascertained. A reduction of L₄ heterochromatin leads to a significant rise both in mean cell chiasma frequency and between cell variance. The effect on chiasma frequency is transchromosomal. The normal pattern of strict chiasma localisation tends to be disrupted in germ lines which include modified L₄ chromosomes. There is a reduction in the number of proximal and distal chiasmata and an increase in the frequency of interstitial ones. It is proposed that the standard L₄ heterochromatin may function in conserving heterozygosity and promoting uniformity between parent and offspring. Partial removal may lead to an effective increase in recombination and produce a greater diversity of genotypes for selection to act upon.     

Supernumerary segments in five species of grasshoppers (Orthoptera: Acridoidea)

Supernumerary segments have been observed in five species of grasshoppers: Calliptamus barbarus, Oedipoda fuscocincta, Acrotylus insubricus, Omocestus raymondi and Chorthippus ariasi. In four cases they are located in the S-chromosomes, but in A. insubricus they are carried by the megameric pair (M₉). In C. barbarus and O. fuscocincta we have observed non-homologous association during diplotene between the extra segments and the X-chromosome. The supernumerary segments of these two species are distally located. However, in anaphase-I the unequal bivalents divide reductionally in 30% and 20% of the cells, respectively. Finally, the supernumerary segments of C. barbarus do not produce any effect on mean chiasma frequency, but they decrease significantly the between-cell variance of chiasmata in males carrying them.     

Karyotype,heterochromatin content and meiotic features ofPoecilocera picta (Orthoptera,Acrididae)

Cytological study of three distinctly separated populations ofPoecilocera picta revealed a chromosome number of 2N = 18 + XO/ XX. Except for the hemizygosity of a procentric heterochromatic block in the M₆ pair of the Bangalore population, the basic karyotype of the three populations is markedly similar. The autosomal karyotype formula is 2Lt + 4Mt + 1 Mst + 2S st and the telocentric X chromosome is the longest of the complement. All bivalents at pachytene carried procentric heterochromatic blocks. The M₄ is the nucleolus organiser with the NOR region situated interstitially but proximal to the centromere. About 11 μm (4%) of the total (290 μm) autosomal pachytene complement is heterochromatic; a major portion of it is contributed by the S₉ pair which is mostly heterochromatic. Chiasmata are localized proximally and distally and in the S₉ pair their formation is confined to the short procentric euchromatic segment of the long arm. Female meiosis did not reveal any chromomere pattern at pachytene and, unlike in the male, the sex bivalent in the female is indistinguishable from the autosomal bivalents. G- and C-banding patterns in males showed procentric bands in all the chromosomes. In addition there are eight telomeric and two interstitial bands which are C negative. The S₉ pair showed only two bands. The G-banding pattern of the sex chromosome in meiosis showed only a centric band while the heterochromatic body of the facultatively heterochromatic X remained G negative.     

Karyotype differences in the crenaticeps-group of Atractomorpha (orthoptera,acridoidea, pyrgomorphidae)

The four known species of the crenaticeps-group of the genus Atractomorpha have 2n ()=18+X0. All members of the complement are rod-chromosomes and the smallest autosome (no. 9) is megameric. The four species have similar amounts of euchromatin but differ markedly in the amount of heterochromatin present in their genomes. In A. similis, A. crenaticeps and the unnamed species, Species-1, there are distinct proximal segments of heterochromatin in the eight large autosomes. In A. similis these chromosomes also have prominent distal segments of heterochromatin. The fourth species, A. australis, has no visible heterochromatin in its eight large autosomes except for a small segment at the proximal end of autosome 4. In all four species, the heterochromatic segments influence chiasma frequency and chiasma position. Moreover the overall chiasma frequency is lowest in A. similis with most heterochromatin and highest in A. australis with least heterochromatin.     

Spontaneous chromosome mutations in Truxaline grasshoppers

Three distinct mutant conditions are described in single male individuals from three species of short horn grasshopper. Of these, one is an entire germ line mutant of Myrmeleotettix maculatus, heterozygous for a centric fusion between single M₄ and M₅ telocentric chromosomes. In contrast, the remaining two mutants are present in mosaic form. One is heterozygous for an L₁-M₄ interchange in Omocestus viridulus, the other tetrasomic for the M₄ chromosome in Chorthippus parallelus which in addition is characterised by the inclusion of a supernumerary heterochromatic segment on one S₈ homologue. Centric fusion in Myrmehotettix maculatus has neither disturbed the chiasma potential of the elements constituting the fusion multiple nor, has it apparently influenced the production of balanced gametes. The pattern of chiasma formation in the L₁-M₄ interchange multiple lends support to the contention that the process of chiasma formation originates near the distal end of chromosome arms in Omocestus viridulus. There is no interaction between the two mutant conditions of tetrasomy and the presence of supernumerary segments in Chorthippus parallelus. Moreover, because of the precocious nature of two of the four M₄ homologues there is little tendency to form multivalents. The two M₄ bivalents share a similar mean chiasma frequency.     

The supernumerary segment system of Stethophyma

Three species of the genus Stethophyma carry supernumerary heterochromatic segments. The European species, S. grossa, has segments located close to the centromere on the S₁₁ chromosome pair, while the North American species, S. lineatum and S. gracile, have both interstitial and terminal segments on the S₁₀ and S₁₁ chromosomes. The latter species show a high degree of segment variation between individuals and the interstitial segments also show variation in size. The presence of segments on the S₁₀ and S₁₁ chromosomes, whether homozygous or heterozygous, modifies the pattern of chiasma distribution in these chromosomes when compared with that found in the basic homozygotes. When interstitial, they also lead to a high frequency of ring bivalents.Two points suggest that interstitially located supernumerary segments may prove to be more common than has previously been accepted. Firstly, combined equational and reductional segregation in unequal bivalents is only otherwise explicable in terms of chiasma formation in a short arm. Secondly the rod chromosomes of many Acridids may well be telocentric as in the case under study.It is proposed that these segments have arisen through a process of duplication with no evidence of interchromosomal movement.On educational leave from the Forest Research Laboratory, Canadian Forestry Service, Fredericton, New Brunswick, Canada.     

Cytogenetic studies on Chorthippus jucundus (Fisch.) (Orthoptera) III. The meiotic consequences of a spontaneous centric fusion

A spontaneous structural heterozygote originated from a centric fusion involving two acrocentric autosomes (M₅ and S₈) in a male Chorthippus jucundus (2n=16+X) was tested for the effects on chiasmata characteristics and the role that these could play in metaphase-I orientation of the trivalent. Results show non-existence of inter- or intra-chromosomal effects on chiasma frequency when compared with standard individuals, and displacement of the single chiasma on the S₈ to a distal position while no significant change is appreciated in the M₅ chiasma distribution. The presence of two chiasmata on the M₅ and one on the S₈ always induces a linear orientation of the trivalent. However, when two chiasmata are present (one on each chromosome) and independently of their location on each arm (proximal, interstitial of distal) any of the possible orientations (linear or convergent) can be attained. The frequency of linear orientation is higher than that expected at random in the resulting trivalent during metaphase-I and the rate of reorientation is very low.The meitotic behaviour of such a trivalent is discussed taking into account the already mentioned aspects together with the size of the fused element.     

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.     

Parallel polymorphism for supernumerary segments inChorthippus parallelus (zetterstedt)

A complex and parallel pattern of polymorphism for heterochromatic supernumerary segments in the M₇ and S₈ chromosomes has been found in 14 populations of the meadow grasshopperChorthippus parallelus. Nine distinct karyotype classes for these two chromosome pairs occur though they are not equally represented in different populations. Populations differ also with respect to the frequency of supernumerary segments they contain. In all populations the presence of supernumerary segments leads to a significant elevation of mean cell chiasma frequency compared to individuals from the same population lacking such segments. The extent of the effect appears to differ in different populations. The observed frequencies of S₈ karyotypes conform to the expectations of a Hardy-Weinberg distribution. Those of the M₇, however, do not, and in all but one of the 14 populations there is a significant excess of homokaryotypes. In the Ashurst population 26% of the individuals sampled were characterised by germ-line polysomy for the M₄ chromosome, either in the form of entire tetrasomics or more usually as mosaics ranging from tri- to hepta-somics. In all these polysomics the M₄ chromosomes in excess of two were regularly heteropycnotic at first meiotic prophase from zygotene to diakinesis. As a consequence of this multivalents are rare. Extra M₄ chromosomes do not modify the chiasma characteristics of the other chromosomes in the complement. Nor do they modify the action of the supernumerary segments in any way.     

Die intraspezifische Variabilität des heterochromatischen Armes eines Chromosoms bei der GattungCarabus L. (Coleoptera)

The chromosome complement ofC. auronitens Fabr. is 2n _♂=26+XY. One autosomal pair—called A-chromosomes—is relatively long.A-chromosomes consist of a euchromatic and a heterochromatic arm. Labelling of mitotic chromosomes with³H-thymidine shows that replication of the heterochromatic arm continues when it has ended in the euchromatic arm. In males and females the length of the heterochromatic arm varies intraindividually. In 47 of 99 males the heterochromatic arms were heteromorphic. Calculations of the quotient length of the euchromatic/length of the heterochromatic arm have shown that at least 6 different types of the A-chromosome exist. These types differ from each other in the number of heterochromatic sections separated by constrictions. The longest heterochromatic arm observed consisted of 8 such sections. The genetic significance of the heterochromatin in the genus ofCarabus is at present unknown (Zusammenfassung see p.305).      

The localization of “ordinary” sex-linked genes in section 20 of the polytene X chromosome of Drosophila melanogaster

A cytogenetic procedure is described whereby a combination of polytene chromosome analysis and complementation mapping has permitted the unequivocal localization of ordinary sex-linked genes (those not covered by the Y-chromosome) in Section 20, the most proximal region of Bridges' (1938) map of the polytene X-chromosome. Thus far, eleven functional units in Section 20 distal to the bobbed locus, but none proximal, have been resolved. We suggest that the polytenized portion of Section 20, which heretofore has traditionally been considered as heterochromatic, corresponds, in fact, with the euchromatic portion of the mitotic X-chromosome.     

Cytogenetic studies of the Australian rodent,Uromys caudimaculatus,a species showing extensive heterochromatin variation

The Australian rodent, Uromys caudimaculatus, consists of two chromosome races, a) The Southern Race is characterized by the possession of two to twelve B-chromosomes. These vary considerably in size, morphology, and C- and G-banding characteristics, they behave as univalent at meiosis and are inherited in a random manner, b) The Northern Race lacks Bchromosomes, but possesses large blocks of distal C-positive heterochromatin on between 18 and 28 of the 46 chromosomes. The C-blocks may be entirely G-positive, entirely G-negative, or G-banded, suggesting heterogeneity within the C-blocks. There is extensive variation both between and within populations of the northern race in the number and size of the distal heterochromatic blocks. There is no apparent difference between the races in chiasma frequency. The northern race does have a much higher proportion of interstitial versus distal chiasmata, although it is probable that this is merely a reflection of lack of crossing over in the heterochromatic blocks rather than an actual shift of chiasma localisation within the euchromatin. Despite the extensive differences between the races in the amount and organization of constitutive heterochromatin, hybrids show no abnormalities at meiosis and they are fully fertile.     

Regional control of nondisjunction of the B chromosome in maize

Control of nondisjunction in the maize B chromosome was studied using a set of B-10 translocations. The study focused on the possible effect of the proximal region of the B long arm. The experimental procedure utilized a combination of a 10^B chromosome from one translocation with a B¹⁰ from another translocation. The breakpoints of the two translocations were so located that combination of the two elements created a deletion in the proximal region of the B chromosome, but no deletion in chromosome 10. Two different types of deletions were established; one involved a portion of the euchromatic region and the other the entire heterochromatic portion comprising the distal half of the B long arm, except for the small euchromatic tip. Deletion of the heterochromatic portion did not exert any effect on nondisjunction. Deletions of different portions of the euchromatic region produce different responses. Some deletions resulted in typical B nondisjunctional activity; others resulted in the disappearance of this activity. It is concluded that a region within the euchromatic portion of the chromosome is critical for the nondisjunction of B chromosomes. Among 22 translocations with breakpoints in the euchromatic regions, three were proximal to the critical region, 16 were distal and the position of three others was not determined.     

The inter-relationship between heterochromatin distribution and chiasma distribution

The distribution of chiasmata and their relationship to the presence of fixed and polymorphic heterochromatic segments is described in seven grasshopper species. In six of these, Cryptobothrus chrysophorus, Trimerotropis bilobata, Calliptamus wattenwylianus, Arcyptera fusca, Pezotettix giorni and Acrotylus insubricus, the presence of terminally located polymorphic heterochromatic segments leads to a radical redistribution of chiasmata away from the segments to more proximal sites. Polymorphisms for proximal heterochromatic segments exist in the first three of these species and they lead to a predominance of terminally associated homologues at male meiosis. In Oxya japonica where both polymorphic and fixed blocks are present, the polymorphic blocks have a similar pronounced effect on chiasma distribution, whereas the fixed blocks have no such effect.     

Contrasting response of euchromatin and heterochromatin to translocation in polytene chromosomes of Drosophila melanogaster

Studies on Feulgen-DNA content in the polytene chromosomes of D. melanogaster T(14)w ^m258-21 heterozygotes showed that when the euchromatic region 3D₁-E₂ is located next to the heterochromatic breakpoint it contains less DNA than in the non-translocated homologue (Hartmann-Goldstein and Cowell, 1976). In contrast to the region adjacent to the breakpoint, region 3C_1–10, which contains intercalary heterochromatin, shows more DNA in the translocated than in the non-translocated chromosome. Transposition may induce morphologically euchromatic regions containing putatively underreplicated sequences to undergo additional replication cycles. Region 2E₁-3A₄, distal to 3C₁ and at some distance from the heterochromatic breakpoint is apparently unaffected. Extended replication and reduced DNA content in regions which have undergone chromosomal rearrangement could be accounted for by varying degrees of blockage of replication in individual strands of the polytene chromosome.     

18 μm replication units of chromosomal DNA fibers of differentiated cells of Pea (Pisum sativum)

A technique is presented for investigating possible early terminalisation of chiasmata, based on the analysis of labelling patterns in autoradiographs in X₂-labelled diplotene bivalents. Terminalisation is expected to produce unlabelled gaps in otherwise labelled bivalents which, given even a moderate amount of movement, is capable of resolution by this technique. The method has been evaluated using diplotene spermatocytes of Schistocerca gregaria as a test system. Very few unlabelled gaps were actually observed in X₂-labelled bivalents, in fact no more than in X₁-labelled bivalents, where chiasma terminalisation is not expected to produce gaps. Consequently it is concluded that the gaps observed are due to technical causes and that early terminalisation is an unimportant factor determining chiasma distribution in this system.     

Studies of Normal and Position-Affected Expression of ROSY Region Genes in DROSOPHILA MELANOGASTER

Transformant complementation, intragenic deletions and Northern blot analyses provide unambiguous localization of the l(3)S12 gene immediately proximal to the 5' end of the rosy locus. We have characterized an array of transformants with respect to l(3)S12 and rosy expression. The l(3)S12 gene is exceedingly sensitive to euchromatic site-specific position effects. Unlike the rosy locus, l(3)S12 is insensitive to heterochromatic position effect in rearrangements, as well as in a transformant located in heterochromatin. Cotransformants for both l(3)S12 and rosy elicit no apparent pattern of concordance with respect to euchromatic site-specific position effects. Heterochromatic-euchromatic rearrangements are examined with respect to position effects on expression of the rosy region genes l(3)12, rosy, snake and piccolo, as well as suppressor effects. Clear distinction is seen between euchromatic and heterochromatic effects.     

Pseudoterminalisation,terminalisation, and non-chiasmate modes of terminal association

Terminal associations occur commonly between meiotic homologues of the two smallest (S10, S11) chromosomes in the northern race of Cryptobothrus chrysophorus when they are either heterozygous or homozygous for distal supernumerary heterochromatic segments. A detailed examination of the origin and behaviour of these associations provides convincing evidence that they are non-chiasmate in character and so cannot be explained by either pseudoterminalisation or terminalisation. The same is true of the terminal associations involved in the persistent pseudomultiples that develop between non-homologues of Heteropternis obscurella when one or both of these carry distal heterochromatic segments. In both situations the C-bands involved in such terminal associations are entire and are never interrupted by non-banded material. In Cryptobothrus, similar associations can also develop between centromere regions when these are heterozygous or homozygous for proximal supernumerary heterochromatic segments.