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T Ashley

Publications and source records attributed to T Ashley.

At least 55 records · Page 3Linked to original sources
PubMed1993

A "hot spot" of recombination coincides with an interstitial telomeric sequence in the Armenian hamster.

The chromosomes of male Armenian hamsters (Cricetulus migratorius) exhibit highly localized terminal and interstitial chiasmata. An interstitial telomeric sequence detected by in situ hybridization was clearly visible at the primary constriction of a large metacentric in both mitotic and meiotic chromosomes. This telomeric sequence was the site of a chiasma in 69% of all 58 diakinesis/metaphase I cells examined. The frequency of meiotic exchange at this site was therefore 34.5%, an extraordinary "hot spot" of recombination. Subsequent chiasma interference can be assumed to reduce recombination and tighten linkage along both arms of male hamster chromosomes. These observations suggest that telomere-promoted recombination may represent a second pathway of recombination, mechanistically different from the more heterodispersed process of meiotic exchange.

Animals↗
PubMed1990

Prediction of mammalian meiotic synaptic and recombinational behavior of inversion heterozygotes based on mitotic breakpoint data and the possible evolutionary consequences.

It has been suggested (Ashley, 1988) that it is possible to predict the meiotic behavior of chromosome aberrations of higher vertebrates based on the position of their breakpoints relative to mitotic band pattern. Evidence supporting this hypothesis and details of the expected synaptic, recombinational, and evolutionary effects of inversion with breakpoints in R-vs. G-bands are elaborated in the current paper.

Animals↗
PubMed1990

Correlation between meiotic behavior and breakpoints with respect to G-bands in two X-4 mouse translocations: T(X;4)7R1 and T(X;4)8R1.

The meiotic synaptic behavior of male mice heterozygous for one of two X-4 translocations was examined to test a recently advanced hypothesis (Ashley, 1988) suggesting that it is possible to predict the synaptic behavior (nonhomologous vs. homologous) and recombinational parameters (suppression vs. nonsuppression of crossing-over) of a chromosome aberration from mitotic G-band breakpoint data. The hypothesis was based on prior observations of synaptic behavior in a series of X-autosome translocations in mice. The breakpoints of the translocation T(X;4)7R1 are both in G-light bands. As predicted by the hypothesis, synapsis was restricted to homology. In contrast, one breakpoint of the translocation T(X;4)8R1 lies in a "stippled" band of the standard diagrams of Nesbitt and Francke (1981). As predicted (Ashley, 1988), "stippled" bands are shown here to synapse nonhomologously, i.e., they behave as "G-dark." The linkage data, as they relate to the synaptic data and the predictions of the hypothesis, are also discussed.

Animals↗
PubMed1990

Axial shortening during pachynema unrelated to nonhomologous synapsis.

The pachytene behavior of chromosomes participating in quadrivalent formation in male mice heterozygous for T(X;4)7Rl or T(X;4)8Rl was analyzed in electron micrographs of microspread spermatocytes. In each population of nuclei from the translocation heterozygotes, the longest 4X axes were approximately the proportional length expected from the respective contributions of the 4 and the X estimated from breakpoint positions in mitotic chromosomes. However, the 4X axis of these translocation quadrivalents undergoes extensive shortening. In both R7 and R8 the shortest 4X axis observed in the population of nuclei was approximately the length of the normal 4 axis. This equalization of axial lengths suggests that there may be an interchromosomal interaction between synapsed chromosomes. In R8, axial shortening of the 4X occurs as pachynema progresses. In both translocations, shortening is accompanied by twisting of the 4X around the 4. Both axial shortening and twists are characteristics exhibited by chromosomal axes of unequal length as part of the meiotic phenomenon described as "synaptic adjustment" (Moses, 1977). Synaptic adjustment involves, in addition, nonhomologous synapsis, which is delayed until the latter part of pachynema. However, axial shortening in R7 and R8 is not accompanied by nonhomologous synapsis. In R7, nonhomologous synapsis does not occur; in R8, it is confined to quadrivalents in which the 4X axis is near its maximum length (i.e., early). This behavior suggests that axial shortening and nonhomologous synapsis during the progression of pachynema (previously considered collectively under the term "synaptic adjustment") are not necessarily coupled events.

Animals↗
PubMed1989

The behavior during pachynema of a normal and an inverted Y chromosome in Microtus agrestis.

The pachytene behavior of the chromosomes of Microtus agrestis (L.) (Rodentia, Arvicolidae) males carrying either the standard, or the pericentrically inverted Lund Y chromosome have been examined by electron microscopy of microspread spermatocytes. There is no synapsis between the X and either the standard or the Lund Y chromosomes during any substage of pachynema. Since synapsis is generally considered a prerequisite for crossing over, there appears to be no opportunity for crossover or chiasma formation between the X and Y in this species. The G-, C- and NOR-banded mitotic karyotypes of animals carrying the standard and Lund Y are also presented.

Animals↗
PubMed1989

Absence of synapsis during pachynema of the normal sized sex chromosomes of Microtus arvalis.

The pachytene behavior of the chromosomes of males of Microtus arvalis (Pall.) (Rodentia, Arvicolidae) was examined by electron microscopy in microspread preparations of spermatocytes. There was no synapsis between the axes of these two chromosomes during this period. Since synapsis is universally considered a prerequisite for crossing over and chiasmata formation, disjunction of the sex chromosomes in this species prerequisite for crossing over and chiasmata formation, disjunction of the sex chromosomes in this species must be presumed to be achiasmatic. Unlike previously examined species with no synapsis or crossing over between the X and Y, the sex chromosomes of M. arvalis are of normal size: the X chromosome is of an "original" X size and the Y is a small acrocentric. C-band studies of M. arvalis mitotic metaphase reveal no blocks of heterochromatin on the sex chromosomes. The implications of these findings are discussed.

Animals↗
PubMed1988

G-band position effects on meiotic synapsis and crossing over.

An examination of synaptic data from a series of X-autosome translocations and crossover data from an extensive series of autosome-autosome translocations and autosomal inversions in mice has lead to the development of a hypothesis which predicts synaptic and recombinational behavior of chromosomal aberrations during meiosis. This hypothesis predicts that in heterozygotes for chromosomal rearrangements that meiotically align G-light chromatin with G-light chromatin lack of homology will be recognized. If homologous synapsis cannot proceed, synaptonemal complex formation will cease and there will be no physical suppression of crossing over in such rearrangements. However, if a chromosomal rearrangement aligns G-light chromatin with G-dark chromatin at the time of synapsis, lack of homology will not be recognized and synaptonemal complex formation will proceed nonhomologously through the G-dark chromatin. Crossing over will be physically suppressed in this region and this suppression of crossing over will be confined to the chromosome in which the G-light chromatin is nonhomologously synapsed with G-dark chromatin. When G-light chromatin is once again aligned with G-light chromatin, lack of homology again will be recognized and either homologous synapsis will be reinitiated (as in an inversion loop), or will cease altogether (as in some translocations). Unlike the previously described "synaptic adjustment", this nonhomologous synapsis of G-light with G-dark chromatin appears to compete with homologous synapsis during early pachynema.

Animals↗
PubMed1987

Nonhomologous synapsis of the XY during early pachynema in In(X)1H male mice.

It has been previously supposed that meiotic synapsis is restricted to homology during early, but not late pachynema. The synaptic behavior of an inverted X chromosome, In(X)1H as reflected in the synaptonemal complexes of the sex chromosomes has been examined in microspread spermatocytes by electron microscopy and evidence of extensive nonhomologous synapsis between the X and Y during early pachynema has been obtained.

Animals↗
PubMed1986

A new type of nonhomologous synapsis in T(X;4)1R1 translocation male mice.

The synaptonemal complexes of T(X;4)1R1 (abbreviated R1) translocation heterozygotes have been examined by electron microscopy and compared with those of two X-7 translocations: R5 and R6. The X chromosome breakpoint of R1 is estimated to lie between 78 and 82% from the proximal end of the X, in the same general region as the R5 and R6 breakpoints. The position of the autosomal breakpoint of R1, like that of R6, is about 30% from the proximal end of the respective autosome. R1 is also similar to R6 in that there is extensive nonhomologous synapsis both in quadrivalents and heteromorphic bivalents. We have recently found that the location of breakpoints with respect to the position of the G-bands appears to be related to the synaptic behavior seen in translocation heterozygotes. If both breaks of a reciprocal translocation lie in G-light bands, as was the case with R5, synapsis is confined to homology. However, if one break lies in or immediately adjacent to a G-dark band, there is nonhomologous synapsis, as occurs with R1 and R6. Comparison of the synaptic behavior of R1 with R5 and R6 leads to the conclusion that this G-band-related nonhomologous synapsis is of a different type than the "synaptic adjustment" phenomenon that has been described by Moses (1977a). This G-band-related nonhomologous synapsis is not substage-specific, but competes with homologous synapsis during zygotene-early pachytene.

Animals↗
PubMed1983

Synaptonemal complex analysis of X-7 translocations in male mice: R2 and R6 quadrivalents.

Synaptonemal complexes of surface-spread spermatocytes of mice heterozygous for reciprocal translocations R2 or R6 between the X-chromosome and chromosome 7 were examined by light and electron microscopy (EM). Measurements of the lengths of all chromosome axes involved in the translocation configurations and of the extent of synapsis were used to calculate the position of the break points of the two translocations. The breaks for R2 were determined to be at 62% of the 7 as measured from the centromere, and at 27% of the X. Quadrivalents were formed almost exclusively. The break points for R6 were calculated to be at 30% of the 7 as measured from the centromere, and at 75% of the X. Although in R6 the break in the X lies within the potential pairing region of the sex chromosomes, univalent Ys were rarely observed (6%). The EM sample of 76 nuclei contained: 42% quadrivalents, 52% heteromorphic bivalents, 4% trivalent plus Y univalent, and 2% X7-7 bivalent plus two univalents (7X and Y). Nonhomologous synapsis occurred in the quadrivalents of both R2 and R6. In R6 nonhomologous synapsis of the X portion of the 7X with the 7 involved up to 14% of the length of the 7. Methods are discussed for determining the position of the break points in the presence of nonhomologous synapsis. It is proposed that the high percentage of bivalents is due to premature desynapsis of the 7X from the 7 and that the X portion of the 7X axis confers its property of premature desynapsis on that portion of the 7 to which it is attached.

Animals↗
PubMed1983

Nonhomologous synapsis of the sex chromosomes in the heteromorphic bivalents of two X-7 translocations in male mice: R5 and R6.

Electron microscopy of pachytene nuclei of mice heterozygous for either of two reciprocal X-7 translocations (R5 or R6) revealed a high frequency of heteromorphic bivalents involving the translocated chromosomes. In both translocations the break was in the proximal third of the 7 and the distal third of the X, but the R5 breaks were closer to the 7 centromere and X telomere than the R6 breaks. In both translocations the 7 frequently synapsed nonhomologously with the X7. In R5 the part of the X to which the 7 synapsed may include a region that synapses with the Y in normal mice. However, in R6 the 7 synapsed with a portion of the X that never synapses with the Y (Synapsis was clearly in the "differentiated" region). In both translocations the Y synapsed maximally with the X portion of the 7X in those nuclei in which there was nonhomologous synapsis of the 7 with the X7. The Y occasionally synapsed nonhomologously with the 7 portion of the 7X. The behavior of the bivalents suggests that the autosomal portions of the 7X and X7 may alter the behavior of the sex-chromosome portions. Both the nonhomologous synapsis of the Y with the 7X and the timing of events during pachytene have led us to question the "homology" between the X and Y in this species.

Animals↗
PubMed1983

Comparison of chromosome associations in human lymphocytes arrested by colcemid, nocodazole, or cycloheximide.

The method of "generalized distances" was applied to compare the effects on homologous interchromosomal distances of colcemid, the routinely used tubulin inhibitor with the effects of two other metaphase arrestants: nocodazole, also a tubulin inhibitor and cycloheximide, an inhibitor of protein synthesis which preserves somatic association. More homologous pairs were associated in the cycloheximide treatment than in the other two procedures; however, while several chromosomes which tend to lie toward the center of the metaphase plate showed somatic association in the various treatments, we found no evidence for somatic association of the larger, more peripherally located chromosomes in human cells in any of our treatments (chromosome pair 7 excepted in the colcemid sample).

Benzimidazoles↗
PubMed1982

Synaptonemal complex analysis of X-7 translocations in male mice. I. R3 and R5 quadrivalents.

The synaptonemal complexes of surface-spread spermatocytes of mice heterozygous for one of two reciprocal translations (R3 and R5) between the X and chromosome 7 have been examined by light and electron microscopy (EM). The break points of R3 were determined to be at 70% of chromosome 7, as measured from the centromere, and at 22% of the X. Translocation quadrivalents were formed almost exclusively. The break points of R5 were at 21% of chromosome 7 as measured from the centromere, and at 83% of the X. There was little indication that the break in the X interfered with sex-chromosome synapsis between the 7X and Y. Univalent Y's were not observed in R3, and only seldom observed (8-14%) in R5. However, in contrast to R3, R5 formed quadrivalents relatively rarely (20% in the EM study of 100 nuclei), and heteromorphic bivalents of 7X-Y and X7-7 quite frequently (72%). Possible causes of this high bivalent frequency are discussed. Light-microscope (LM) analysis alone was found to be inadequate for interpreting synaptic configurations (quadrivalents vs. bivalents) in R5. The LM analysis was further complicated by the occurrence of nonhomologous synapsis in the heteromorphic bivalents of R5, a phenomenon easily recognized and interpreted in the EM portion of the study.

Animals↗
PubMed1981

Fine structure and behaviour of a pericentric inversion in the sand rat, Psammomys obesus.

In pachytene spermatocytes of the sand rat, Psammomys obesus, a long autosomal bivalent was observed, which was asynaptic for a large interstitial segment of its length in early pachytene. This bivalent also exhibited unaligned kinetochores. In late pachytene spermatocytes all autosomal bivalents were fully synapsed, but one of the shortest bivalents now possessed unaligned kinetochores. Evidence is presented in support of the proposition that the asynaptic interstitial region observed in early pachytene is due to the bivalent being heterozygous for a pericentric inversion. Using the maximum extent of homologous pairing, the break points were mapped at 26% from one end and 20% from the other. The unaligned kinetochores support the proposal that the aberration is an inversion and measurements of their positions confirm the estimated break points. In one cell a bivalent with interstitial (but no terminal) synapsis also confirms the inversion hypothesis. It is proposed that the bivalent is so small that topological considerations prevent the formation of the expected inversion loop. Evidence is also presented that complete synapsis of the bivalent during late pachytene can be attributed so 'synaptic adjustment', characterized by non-homologous synapsis (heterosynapsis). The position of the aberrant bivalent in relation to the sex chromosomes also changes during pachytene. When the bivalent is incompletely synapsed it generally associates by its ends with the ends of the sex chromosomes, but when it is non-changes during pachytene. When the bivalent is incompletely synapsed it generally associates by its ends with the ends of the sex chromosomes, but when it is non-homologously synapsed it is not associated with them.

Animals↗
PubMed1980

End association and segregation of the achiasmatic X and Y chromosomes of the sand rat, Psammomys obesus.

In Psammomys obesus there is no pairing between the X and Y chromosomes and no chiasma formation (Solari and Ashley, 1977). It is demonstrated that ends of the axial elements of the X and Y chromosomes come together during pachytene, and regularly form at least one end-to-end junction. This achiasmatic physical connection between the ends of the X and Y persists until anaphase I, thus assuring the normal distribution of the sex chromosomes observed by light microscopy. In addition, there are no differentiations of the axes of the X and Y similar to those observed in other mammalian species thus far examined, a fact that could influence chromatid cohesiveness and disjunction.

Animals↗
PubMed1979

Specific end-to-end attachment of chromosomes in Ornithogalum virens.

C-banding of nonhomologous chromosomes in haploid generative nuclei of Ornithogalum virens (n = 3) reveals a high degree of specificity with respect to end-to-end connexions. The centromeric end of chromosome 2 preferentially associates with the centromeric end of chromosome 3 and the telomeric end of chromosome 3 associates preferentially with the telomeric end of chromosome 1. This same association of nonhomologous chromosomes persists in prophase nuclei of diploid root tips. In addition, the telomeric ends of the 2 chromosome 2s are connected to one another as are the centromeric ends of the chromosome 1s. This results in a ring of chromosomes in which homologues lie opposite one another. Centromeric ends lie on one side of the nucleus and telomeric ends on the other. It is proposed that this specific association of chromosome ends reflects an order which was probably established at the preceding anaphase or telophase and which persists throughout interphase. The suggestion is made that the proximity of homologous ends and consequently homologous alignment may facilitate initiation of pairing at meiosis.

Cell Division↗