Two permanent linear chains of sex chromosomes in Neotermes fulvescens and karyotypes of two other neotropical Kalotermitidae species (Insecta, Isoptera)

Genome ◽  
1995 ◽  
Vol 38 (5) ◽  
pp. 958-967 ◽  
Author(s):  
Vanderlei Geraldo Martins ◽  
Alejo Mesa
Keyword(s):  
Sex Chromosomes ◽  
Diploid Number ◽  
Linear Chain ◽  
Neotropical Region ◽  
Male Meiosis ◽  
The Other ◽  
South American ◽  
Y Chromosomes ◽  
Linear Chains ◽  
Males And Females

Meiosis and (or) mitosis of males and females of Cryptotermes brevis, Eucryptotermes wheeleri, and Neotermes fulvescens, all of them from the neotropical region, were analyzed. Cryptotermes brevis showed a similar karyotype to that obtained by other authors for specimens of the neartic and Australian regions (2n = 36 for females and 2n = 37 for males, with XX and XYY sex mechanisms, respectively). Eucryptotermes wheeleri, the only species that has been described in this genus, showed the lowest number of chromosomes reported for Isoptera (2n = 22) until now. The male meiosis of this species presents a linear chain of six sex chromosomes, three of them being X and three of them Y chromosomes. Neotermes fulvescens showed a diploid number of 40 for males and 42 for females and, in the first male meiosis, two linear chains of chromosomes, both related to sex. One of the chains, named A, presented nine chromosomes and the other, named B, seven chromosomes. Hypotheses to explain these mechanisms are formulated in this paper and putative ancestral relationships with other species of Kalotermitidae are presented.Key words: termite, Neotermes, two linear chains, translocations, South American.

Pattern of X-Y chromosome pairing in the Taiwan vole, Microtus kikuchii

Genome ◽  
2001 ◽  
Vol 44 (1) ◽  
pp. 27-31 ◽  
Author(s):  
K Mekada ◽  
M Harada ◽  
L K Lin ◽  
K Koyasu ◽  
P M Borodin ◽  
...  
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Sex Chromosomes ◽  
Meiotic Prophase ◽  
Organizer Region ◽  
Nucleolar Organizer Region ◽  
Nucleolar Organizer ◽  
The Other ◽  
Banding Patterns ◽  
Y Chromosomes

Pairing of X and Y chromosomes at meiotic prophase and the G- and C-banding patterns and nucleolar organizer region (NOR) distribution were analyzed in Microtus kikuchii. M. kikuchii is closely related to M. oeconomus and M. montebelli, karyologically and systematically. The formation of a synaptonemal complex between the X and Y chromosomes at pachytene and end-to-end association at diakinesis – metaphase I are only observed in three species in the genus Microtus; M. kikuchii, M. oeconomus, and M. montebelli. All the other species that have been studied so far have had asynaptic X–Y chromosomes. These data confirm that M. kikuchii, M. oeconomus, and M. montebelli are very closely related, and support the separation of asynaptic and synaptic groups on the phylogenetic tree.Key words: Microtus kikuchii, Microtus phylogeny, karyotype, synaptic sex chromosomes, synaptonemal complex.

Y chromosome specific markers and the evolution of dioecy in the genus Silene

Genome ◽  
1998 ◽  
Vol 41 (2) ◽  
pp. 141-147 ◽  
Author(s):  
Y Hi Zhang ◽  
Veronica S Stilio ◽  
Farah Rehman ◽  
Amy Avery ◽  
David Mulcahy ◽  
...  
Keyword(s):  
Y Chromosome ◽  
Sex Chromosomes ◽  
Silene Latifolia ◽  
Dioecious Species ◽  
Sequence Characterized Amplified Region ◽  
Y Chromosomes ◽  
Heteromorphic Sex Chromosomes ◽  
Males And Females ◽  
Genus Silene ◽  
Evolution Of Dioecy

Sex determination in plants has been most thoroughly investigated in Silene latifolia, a dioecious species possessing heteromorphic sex chromosomes. We have identified several new Y chromosome linked RAPD markers and converted these to more reliable sequence characterized amplified region (SCAR) markers by cloning the RAPD fragments and developing longer primers. Of the primer pairs for seven SCARs, five amplify a single, unique fragment from the DNA of male S. latifolia. Two sets of primers also amplify additional fragments common to males and females. Homology between the X and Y chromosomes is sufficient to allow the amplification of fragments from females under less stringent PCR conditions. Five of the SCARs also distinguish between the sexes of closely related dioecious taxa of the section Elisanthe, but not between the sexes of distantly related dioecious species. These markers will be useful for continued investigations into the evolution of sex, phylogenetic relationships among taxa, and population dynamics of sex ratios in the genus Silene.Key words: Melandrium, RAPDs, sex chromosomes, SCARs.

scholarly journals Sexually dimorphic recombination can facilitate the establishment of sexually antagonistic polymorphisms in guppies

2018 ◽  
Author(s):  
Roberta Bergero ◽  
Jim Gardner ◽  
Beth Bader ◽  
Lengxob Yong ◽  
Deborah Charlesworth
Keyword(s):  
Sex Chromosomes ◽  
Poecilia Reticulata ◽  
Common Ancestor ◽  
Sex Chromosome ◽  
Empirical Support ◽  
Male Meiosis ◽  
Sexually Dimorphic ◽  
Sex Linkage ◽  
Recombination Suppression ◽  
Males And Females

Summary/AbstractRecombination suppression between sex chromosomes is often stated to evolve in response to polymorphisms for mutations that affect fitness of males and females in opposite directions (sexually antagonistic, or SA, mutations), but direct empirical support is lacking. The sex chromosomes of the fish Poecilia reticulata (the guppy) carry SA polymorphisms, making them excellent for testing this hypothesis for the evolution of sex linkage. We resequenced genomes of male and female guppies and, unexpectedly, found that variants on the sex chromosome indicate no extensive region with fully sex-linked genotypes, though many variants show strong evidence for partial sex linkage. We present genetic mapping results that help understand the evolution of the guppy sex chromosome pair. We find very different distributions of crossing over in the two sexes, with recombination events in male meiosis detected only at the tips of the chromosomes. The guppy may exemplify a route for sex chromosome evolution in which low recombination in males, likely evolved in a common ancestor, has facilitated the establishment of sexually antagonistic polymorphisms.

Sex Chromosome Translocations

2018 ◽  
Author(s):  
R. J McKinlay Gardner ◽  
David J Amor
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Transcriptional Silencing ◽  
The Other ◽  
X Chromosomes ◽  
Chromosome Form ◽  
Chromosome Translocations ◽  
Y Chromosomes ◽  
Autosomal Translocation

The sex chromosomes (gonosomes) are different, and sex chromosome translocations need to be considered separately from translocations between autosomes. A sex chromosome can engage in translocation with an autosome, with the other sex chromosome, or even with its homolog. The qualities of the sex chromosomes have unique implications in terms of the genetic functioning of gonosome-autosome translocations. This chapter acknowledges the specific peculiarities that the sex chromosomes imply: the X being subject to transcriptional silencing; and the very small Y gene complement being confined largely to sex-determining loci. It reviews translocations between sex chromosomes and autosomes; between X and Y chromosomes; and even the very rare circumstance of between X chromosomes and between Y chromosomes. The differences in assessing risk, according to chromosome form, in comparison with the autosomal translocation, are reviewed, and the biology behind these differences is discussed.

Sex Chromosomes and Psychosis

1988 ◽  
Vol 153 (5) ◽  
pp. 675-683 ◽  
Author(s):  
T. J. Crow
Keyword(s):  
Sex Chromosomes ◽  
Distal Segment ◽  
Depressive Illness ◽  
Male Meiosis ◽  
High Rate ◽  
Pseudoautosomal Region ◽  
Psychiatric Disease ◽  
Same Sex ◽  
Y Chromosomes ◽  
Gender Influences

Although the incidence of the recurrent psychoses (bipolar affective illness and schizophrenia) in the two sexes is approximately equal, gender influences a number of aspects of major psychiatric disease: unipolar depressive illness is twice as common in females, onset of schizophrenia is earlier and outcome is worse in males, and pairs of psychotic first-degree relatives are more often than expected of the same sex. In addition, sex chromosomal aneuploidies (e.g. XXY and XXX) are more frequent in patients with psychosis. Some of these findings can be explained if there is a major locus of predisposition to psychiatric disease in the ‘pseudoautosomal’ region of the sex chromosomes – that distal segment of the short arms in which there is genetic exchange between X and Y chromosomes at male meiosis. A gene located here would be transmitted in an autosomal manner, but would be passed above chance expectation to children of the same sex when inherited through a male. In that this segment of the sex chromosomes is subject to a high rate of recombination (which could generate new mutations), and may include determinants of brain lateralisation, it appears that the pseudoautosomal region could carry the genes which predispose to the major psychoses.

Pattern of X–Y chromosome pairing in the Japanese field vole, Microtus montebelli

Genome ◽  
1997 ◽  
Vol 40 (6) ◽  
pp. 829-833 ◽  
Author(s):  
P. M. Borodin ◽  
M. B. Rogatcheva ◽  
K. Koyasu ◽  
K. Fukuta ◽  
K. Mekada ◽  
...  
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Chromosomal Evolution ◽  
The Other ◽  
Field Vole ◽  
Y Chromosomes ◽  
The One ◽  
Ancestral Type

Pairing of X and Y chromosomes at meiotic prophase in males of Microtus montebelli was analyzed. The sex chromosomes form a synaptonemal complex at pachytene and end-to-end association at diakinesis – metaphase I in two species of the genus Microtus (M. montebelli and M. oeconomus) only, while they do not pair at all in the other species of this genus that have been studied so far. These data confirm that M. montebelli and M. oeconomus are very closely related in their origin. It is suggested that the sex chromosomes of M. montebelli and M. oeconomus display the ancestral type of X–Y pairing. The lack of X–Y pairing in most species of Microtus appeared after the split in lineage that led to M. oeconomus and M. montebelli on the one hand and the remaining species on the other.Key words: Microtus montebelli, arvicoline phylogeny, synaptic sex chromosome, synaptonemal complex, chromosomal evolution.

HOMOGAMETIC HETEROSIS IN CROSSBREEDING EXPERIMENTS WITH SHEEP

1970 ◽  
Vol 50 (2) ◽  
pp. 377-384 ◽  
Author(s):  
M. H. FAHMY
Keyword(s):  
Birth Weight ◽  
Sex Chromosomes ◽  
Good Evidence ◽  
Weaning Weight ◽  
Y Chromosomes ◽  
Males And Females ◽  
The Difference ◽  
Breed Crosses ◽  
Daily Gain

Data from two crossbreeding experiments with sheep were analyzed to test the difference in heterosis between males and females in the F1, backcross, and three-breed crosses. The characters studied were birth and weaning weights and preweaning daily gain. In the F1 no marked differences in heterosis in weaning weight and preweaning gain were observed between sexes while in birth weight the two experiments gave conflicting results. In backcrosses and the three-breed crosses, females showed higher heterosis than males in the three characters studied. The ratios of heterosis in males to that in females did not support the hypothesis that differences between sexes in heterosis are due to the action of the sex chromosomes. The results of the two experiments suggested a possible interaction between the X and Y chromosomes of different breeds. The results in general did not give good evidence of homogametic heterosis in crossbreeding experiments with sheep.

scholarly journals Sex chromosomes, sex ratios and sex gaps in longevity in plants

2021 ◽  
Author(s):  
Gabriel AB Marais ◽  
Jean-Francois Lemaitre
Keyword(s):  
Sex Chromosomes ◽  
Statistical Power ◽  
Sex Chromosome ◽  
Sex Ratios ◽  
Y Chromosomes ◽  
Adult Sex Ratio ◽  
Female Longevity ◽  
Males And Females ◽  
The Relationship

In animals, males and females can display markedly different longevity (also called sex gap in longevity, SGLs). Recent work has revealed that sex chromosomes contribute to establishing these SGLs. X-hemizygosity and toxicity of the Y chromosomes are two mechanisms that have been suggested to reduce male longevity (Z-hemizygosity and W toxicity in females in ZW systems). In plants, SGLs are known to exist but the role of sex chromosomes remains to be established. Here, by using adult sex ratio as a proxy for measuring SGLs, we explored the relationship between sex chromosome and SGLs across 43 plant species. Based on the knowledge recently accumulated in animals, we specifically asked whether: (i) species with XY systems tend to have female-biased sex ratios (reduced male longevity) and species with ZW ones tend to have male-biased sex ratios (reduced female longevity), and (ii) this patterns was stronger in heteromorphic systems compared to homomorphic ones. Our results tend to support these predictions although we lack statistical power because of a small number of ZW systems and the absence of any heteromorphic ZW system in the dataset. We discuss the implications of these findings, which we hope will stimulate further research on sex-differences in lifespan and ageing across plants.

scholarly journals Sex chromosome pairing mediated by euchromatic homology in Drosophila male meiosis

2019 ◽  
Author(s):  
Christopher A. Hylton ◽  
Katie Hansen ◽  
Andrew Bourgeois ◽  
John E. Tomkiel
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Intergenic Spacer ◽  
Male Meiosis ◽  
Early Prophase ◽  
Dna Breaks ◽  
Late Prophase ◽  
Prophase I ◽  
Y Chromosomes ◽  
Meiosis I

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.

Description of immature stages and redescription of adults of Ixodes luciae Sénevet (Acari: Ixodidae)

Zootaxa ◽  
2010 ◽  
Vol 2495 (1) ◽  
pp. 53 ◽  
Author(s):  
VALERIA C. ONOFRIO ◽  
MARCELO B. LABRUNA ◽  
JOÃO LUIZ H. FACCINI ◽  
DARCI M. BARROS-BATTESTI
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
First Generation ◽  
Neotropical Region ◽  
The Other ◽  
Immature Stages ◽  
Haller's Organ ◽  
Northern Brazil ◽  
Males And Females ◽  
Scanning Electron

The tick Ixodes luciae occurs in many countries within the Neotropical region but only adult ticks have been morphologically described. Larvae and nymphs parasitize marsupials and rodents while adults are common on marsupials. A colony of I. luciae was obtained from females collected on marsupials from the State of Rondônia, Northern Brazil. After being fed on rabbits, the specimens were maintained under controlled conditions of temperature and humidity. Unfed larvae, nymphs, males and females of the first generation were cleaned and prepared for both optical and scanning electron microscopy. Ixodes luciae is closely related to Ixodes loricatus, Ixodes schulzei, and Ixodes amarali, although each species has its own array of distinctive characters. The larva of I. luciae differs from those of both I. schulzei and I. amarali in the length of the capitulum and from I. schulzei in the number of posthalleral setae in the Haller’s organ. Nymphs differ from I. amarali, I. loricatus and I. schulzei by the length of the external spur on coxae I, and from I. schulzei and I. amarali in having slender and shorter capitulum and hypostome. Males and females of I. luciae differ from the other three species by the length of the external spur on coxae I and by the scutal punctations, which are much longer and larger, respectively, in I. luciae. However, except for a few features, the chaetotaxy is the same for larvae of the four species, not only on the idiosoma (e.g. scutum with four pairs of setae), palpi and tarsus I, but also the number of porose setae within the capsule of Haller’s organ and the prehalleral setae.

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