The pattern of sex chromosome kinetochore phosphorylation during nonrandom segregation in a flea beetle

2000 ◽  
Vol 78 (2) ◽  
pp. 93-98
Author(s):  
Holly Kupfer ◽  
Dwayne Wise

In the flea beetle species, Alagoasa bicolor, males have two sex chromosomes, X and Y, each of which is larger than the rest of the genome combined. These large sex chromosomes do not pair at meiosis I, and are therefore not joined at metaphase I. Nevertheless, they always segregate from each other at anaphase I. As prometaphase I progresses, the unpaired X and Y undergo reorientation from a parallel to a linear configuration. Using 3F3/2, an antibody that detects the level of phosphorylation of a kinetochore protein or proteins, we have determined that this reorientation is not accompanied by a change in the level of phosphorylation of the kinetochores of either X or Y. This implies that: i) either the reorientation does not involve the loss or gain of kinetochore microtubules, or ii) if such loss or gain occurs, it does not effect a change in the tension placed on the nonrandomly segregating kinetochores, or iii) the sex chromosomes, as in some other species, have lost the ability to sense kinetochore tension changes. Evolution of nonrandom segregation may necessitate the inability of the participating chromosomes to affect the metaphase checkpoint. Key words: nonrandom segregation, sex chromosomes, kinetochores.

Genome ◽  
1987 ◽  
Vol 29 (1) ◽  
pp. 76-79 ◽  
Author(s):  
D. G. Bedo

Meiosis and mitosis was studied in males of the primitive termite Mastotermes darwiniensis, which is closely related to the Dictyoptera. In mitotic metaphase cells 98 chromosomes were found with a matching 49 bivalents at metaphase I. Mastotermes darwiniensis has a largely acrocentric karyotype with no sex-linked translocation complexes, like those found in many other termite species, or other sex chromosome differentiation. These observations suggest that ancestral termites probably had karyotypes with many small chromosomes lacking sex chromosome differentiation and that there is no connection between the evolution of sex-linked translocation complexes and eusociality. Key words: sex chromosomes, Mastotermes, termites, eusociality.


Genome ◽  
2000 ◽  
Vol 43 (3) ◽  
pp. 521-527
Author(s):  
Holly Kupfer ◽  
Dwayne Wise

We have analyzed autosome, sex chromosome, and spindle behavior in spermatocytes of the flea beetle, Alagoasa bicolor. In this species, males have very large X and Y chromosomes, which, although they are never physically connected, always segregate to opposite spindle poles at anaphase I, thus preserving the sex ratio in the next generation. We find that the sex chromosomes are partitioned to a peripheral spindle domain early in prometaphase I and that their segregation can be accounted for mainly by their reorientation from the parallel to the linear configuration, and little by chromosome-to-pole movement. Further, the behavior of the autosomes and that of the sex chromosomes seem to have little to do with each other. Spindle elongation is minimal; barely segregating the large sex chromosomes into the daughter cells at telophase I.Key words: nonrandom segregation, sex chromosomes, kinetochores.


1990 ◽  
Vol 56 (2-3) ◽  
pp. 129-133 ◽  
Author(s):  
Charles Tease

SummaryKaryotypic investigation of a phenotypically normal but sterile male mouse showed the presence of an XYY sex chromosome constitution. The synaptic behaviour of the three sex chromosomes was examined in 65 pachytene cells. The sex chromosomes formed a variety of synaptic configurations: an XYY trivalent (40%); an XY bivalent and Y univalent (38·5%); an X univalent and YY bivalent (13·8%); or X, Y, Y univalence (7·7%). There was considerable variation in the extent of synapsis and some of the associations clearly involved nonhomologous pairing. These observations have been compared with previously published information on chromosome configurations at metaphase I from other XYY males.


Genetics ◽  
2001 ◽  
Vol 157 (1) ◽  
pp. 273-281 ◽  
Author(s):  
John E Tomkiel ◽  
Barbara T Wakimoto ◽  
Albert Briscoe

Abstract In recombination-proficient organisms, chiasmata appear to mediate associations between homologs at metaphase of meiosis I. It is less clear how homolog associations are maintained in organisms that lack recombination, such as male Drosophila. In lieu of chiasmata and synaptonemal complexes, there must be molecules that balance poleward forces exerted across homologous centromeres. Here we describe the genetic and cytological characterization of four EMS-induced mutations in teflon (tef), a gene involved in this process in Drosophila melanogaster. All four alleles are male specific and cause meiosis I-specific nondisjunction of the autosomes. They do not measurably perturb sex chromosome segregation, suggesting that there are differences in the genetic control of autosome and sex chromosome segregation in males. Meiotic transmission of univalent chromosomes is unaffected in tef mutants, implicating the tef product in a pairing-dependent process. The segregation of translocations between sex chromosomes and autosomes is altered in tef mutants in a manner that supports this hypothesis. Consistent with these genetic observations, cytological examination of meiotic chromosomes suggests a role of tef in regulating or mediating pairing of autosomal bivalents at meiosis I. We discuss implications of this finding in regard to the evolution of heteromorphic sex chromosomes and the mechanisms that ensure chromosome disjunction in the absence of recombination.


2019 ◽  
Author(s):  
Christopher A. Hylton ◽  
Katie Hansen ◽  
Andrew Bourgeois ◽  
John E. Tomkiel

ABSTRACTTo maintain proper ploidy, haploid sex cells must undergo two subsequent meiotic divisions. During meiosis I, homologs pair and remain conjoined until segregation at anaphase. Drosophila melanogaster spermatocytes are unique in that the canonical events of meiosis I including synaptonemal complex (SC) formation, double-strand DNA breaks, and chiasmata are absent. Sex chromosomes pair at intergenic spacer sequences within the heterochromatic rDNA while euchromatin is required to pair and segregate autosomal homologies, suggesting that pairing may be limited to specific sequences. However, previous work generated from genetic segregation assays or observations of late prophase I/prometaphase I chromosome associations fail to differentiate pairing from conjunction. Here, we separately examined the capability of X euchromatin to pair and conjoin using an rDNA-deficient X and a series of Dp(1;Y) chromosomes. Genetic assays showed that duplicated X euchromatin can substitute for endogenous rDNA pairing sites. Segregation was not proportional to homology length, and pairing could be mapped to nonoverlapping sequences within a single Dp(1;Y). Using fluorescent in situ hybridization (FISH) to early prophase I spermatocytes, we showed that pairing occurred with high fidelity at all homologies tested. Pairing was unaffected by the presence of X rDNA, nor could it be explained by rDNA magnification. By comparing genetic and cytological data, we determined that centromere proximal pairings were best at segregation. Segregation was dependent on the conjunction protein Stromalin in Meiosis while the autosomal-specific Teflon was dispensable. Overall, our results suggest that pairing may occur at all homologies, but there may be sequence or positional requirements for conjunction.ARTICLE SUMMARYDrosophila males have evolved a unique system of chromosome segregation in meiosis that lacks recombination. Chromosomes pair at selected sequences suggesting that early steps of meiosis may also differ in this organism. Using Y chromosomes carrying portions of X material, we show that pairing between sex chromosomes can be mediated by sequences other than the previously identified rDNA pairing sites. We propose that pairing may simply be homology-based and may not differ from canonical meiosis observed in females. The main difference in males may be that conjunctive mechanisms that join homologs in the absence of crossovers.


2003 ◽  
Vol 83 (3) ◽  
pp. 375-384 ◽  
Author(s):  
D. L. Garner ◽  
G. E. Seidel Jr.

Development of flow cytometry for sorting mammalian sperm according to their sex chromosomes began in the late 1970s and early 1980s. This technology, which has recently been commercialized for bovine sperm, is based on the differences in DNA content between X- and Y-chromosome-bearing sperm. Under ideal conditions, 5000 live bovine sperm of each sex can be sorted per second at 90% accuracy. Pregnancy rates of 50% have been achieved routinely in well-managed heifers with sex-sorted, cryopreserved bovine sperm compared to 60–80% with unsexed control sperm. About 90% of offspring have been of the selected sex. Sorting sperm according to sex chromosome content is similarly successful in many other mammals including exotic species, but sorting efficiencies are somewhat less for sperm from some species. Key words: Mammals, sex chromosomes, flow cytometer, cell sorter, DNA content, X and Y sperm, Hoechst 33342


Genome ◽  
1987 ◽  
Vol 29 (2) ◽  
pp. 319-325 ◽  
Author(s):  
Peter Luykx

Collections of colonies of the termite Incisitermes schwarzi from mangroves around the coast of Jamaica revealed six chromosomal types, all involving variations or rearrangements of the sex chromosomes. One of the types had a heteromorphic sex bivalent in which the Y chromosome was larger than the X. The other five races had complex interchange multiples: a chain of 11, a chain of 12, a ring of 12, a ring of 14, and a ring of 18 chromosomes. The situation is similar to that described previously for Kalotermes approximatus, another member of the family Kalotermitidae, in the southeastern United States. The different chromosomal types can be arranged in an evolutionary series, each step requiring an interchange or fusion between an autosome and a previously existing sex chromosome. Such polymorphic chromosome systems, containing Y-segregating elements of different evolutionary ages, may offer an unusual opportunity for studying the sequence of changes accompanying the evolution of Y chromosomes. Key words: termite, Incisitermes, sex-linkage, translocation, interchange, Jamaica.


2020 ◽  
Vol 12 (4) ◽  
pp. 243-258 ◽  
Author(s):  
Wen-Juan Ma ◽  
Fantin Carpentier ◽  
Tatiana Giraud ◽  
Michael E Hood

Abstract Degenerative mutations in non-recombining regions, such as in sex chromosomes, may lead to differential expression between alleles if mutations occur stochastically in one or the other allele. Reduced allelic expression due to degeneration has indeed been suggested to occur in various sex-chromosome systems. However, whether an association occurs between specific signatures of degeneration and differential expression between alleles has not been extensively tested, and sexual antagonism can also cause differential expression on sex chromosomes. The anther-smut fungus Microbotryum lychnidis-dioicae is ideal for testing associations between specific degenerative signatures and differential expression because 1) there are multiple evolutionary strata on the mating-type chromosomes, reflecting successive recombination suppression linked to mating-type loci; 2) separate haploid cultures of opposite mating types help identify differential expression between alleles; and 3) there is no sexual antagonism as a confounding factor accounting for differential expression. We found that differentially expressed genes were enriched in the four oldest evolutionary strata compared with other genomic compartments, and that, within compartments, several signatures of sequence degeneration were greater for differentially expressed than non-differentially expressed genes. Two particular degenerative signatures were significantly associated with lower expression levels within differentially expressed allele pairs: upstream insertion of transposable elements and mutations truncating the protein length. Other degenerative mutations associated with differential expression included nonsynonymous substitutions and altered intron or GC content. The association between differential expression and allele degeneration is relevant for a broad range of taxa where mating compatibility or sex is determined by genes located in large regions where recombination is suppressed.


2021 ◽  
pp. 1-9
Author(s):  
Chiao Kuwana ◽  
Hiroyuki Fujita ◽  
Masataka Tagami ◽  
Takanori Matsuo ◽  
Ikuo Miura

The sex chromosomes of most anuran amphibians are characterized by homomorphy in both sexes, and evolution to heteromorphy rarely occurs at the species or geographic population level. Here, we report sex chromosome heteromorphy in geographic populations of the Japanese Tago’s brown frog complex (2n = 26), comprising Rana sakuraii and R. tagoi. The sex chromosomes of R. sakuraii from the populations in western Japan were homomorphic in both sexes, whereas chromosome 7 from the populations in eastern Japan were heteromorphic in males. Chromosome 7 of R. tagoi, which is distributed close to R. sakuraii in eastern Japan, was highly similar in morphology to the Y chromosome of R. sakuraii. Based on this and on mitochondrial gene sequence analysis, we hypothesize that in the R. sakuraii populations from eastern Japan the XY heteromorphic sex chromosome system was established by the introduction of chromosome 7 from R. tagoi via interspecies hybridization. In contrast, chromosome 13 of R. tagoi from the 2 large islands in western Japan, Shikoku and Kyushu, showed a heteromorphic pattern of constitutive heterochromatin distribution in males, while this pattern was homomorphic in females. Our study reveals that sex chromosome heteromorphy evolved independently at the geographic lineage level in this species complex.


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