The Chromosomal Basis of Sex-Differentiation in Marsupials

1989 ◽  
Vol 37 (3) ◽  
pp. 451 ◽  
Author(s):  
GB Sharman ◽  
RL Hughes ◽  
DW Cooper

Data on ten intersexual marsupials, eight of which were of known karyotype, are presented and reviewed. Three of the intersexes were known or suspected XO/XX or XO/XX/XXX, two were XXY, one was XXY/XY/XX and two were XY in sex chromosome constitution. In all three intersexes which had an XO cell line, but in which no Y chromosome was found in any cell, a small empty scrotum was found to one side of the midline or in the midline. Those which had a non-midline scrotum had mammary tissue on the opposite side and a partial or complete pouch. The intersex with the midline scrotum had no pouch or mammary glands. Unilateral or bilateral putative spermatic cords, not containing a ductus deferens, descended to the scrotum, but in all other respects the internal reproductive systems were like those of normal XX female marsupials. Intersexes with no Y chromosome were of female body size when adult. The XXY and XXY/XY/XX intersexes all had complete pouches and mammary glands and none had a scrotum. All had well developed male internal reproductive systems and undescended testis-like gonads, and were of intermediate body size. Both XY intersexes also had complete pouches and mammary glands, no scrotum, and male-type internal reproductive systems with undescended testes which were normal except for absence of post- primary spermatocyte stages of spermatogenesis. One XY intersex was fully adult and it did not differ from normal XY males of the same species in body measurements, body weight and secondary sex coloration. One of the intersexes of unknown karyotype, but of suspected XX chromosome constitution, was morphologically like the XO/XX/XXX mosaic with a centrally placed scrotum. The other, of suspected XY chromosome constitution, was essentially comparable to the XY intersexes. The data are interpreted, at the whole chromosome level, as follows. In the presence of a single active X chromosome scrotal and spermatic cord development were initiated, whereas they were inhibited in the presence of two X chromosomes. Complete scrotal development completely inhibited, and unilateral scrotal development partly inhibited, pouch and mammary gland development. The Y chromosome was responsible for primary gonadal sex and, apparently through production of MIS, eliminated the Miillerian (i.e. female) sex ducts. Development of a male type of reproductive system was dependent on presence of a Y chromosome and, apparently, androgen production from testes or testis-like gonads. At the gene level the data may be interpreted in terms of a hypothetical S or 'switch' locus, carried on the X chromosome, which induced scrotal development in single dose and a pouch and mammary glands in double dose. If this hypothesis is correct, it would explain the occurrence of incomplete X-chromosome inactivation in marsupials; complete X-inactivation is impossible in marsupials because it would leave each female with a scrotum, not a pouch.

2020 ◽  
Vol 12 (558) ◽  
pp. eaaz5677 ◽  
Author(s):  
Emily J. Davis ◽  
Lauren Broestl ◽  
Samira Abdulai-Saiku ◽  
Kurtresha Worden ◽  
Luke W. Bonham ◽  
...  

A major sex difference in Alzheimer’s disease (AD) is that men with the disease die earlier than do women. In aging and preclinical AD, men also show more cognitive deficits. Here, we show that the X chromosome affects AD-related vulnerability in mice expressing the human amyloid precursor protein (hAPP), a model of AD. XY-hAPP mice genetically modified to develop testicles or ovaries showed worse mortality and deficits than did XX-hAPP mice with either gonad, indicating a sex chromosome effect. To dissect whether the absence of a second X chromosome or the presence of a Y chromosome conferred a disadvantage on male mice, we varied sex chromosome dosage. With or without a Y chromosome, hAPP mice with one X chromosome showed worse mortality and deficits than did those with two X chromosomes. Thus, adding a second X chromosome conferred resilience to XY males and XO females. In addition, the Y chromosome, its sex-determining region Y gene (Sry), or testicular development modified mortality in hAPP mice with one X chromosome such that XY males with testicles survived longer than did XY or XO females with ovaries. Furthermore, a second X chromosome conferred resilience potentially through the candidate gene Kdm6a, which does not undergo X-linked inactivation. In humans, genetic variation in KDM6A was linked to higher brain expression and associated with less cognitive decline in aging and preclinical AD, suggesting its relevance to human brain health. Our study suggests a potential role for sex chromosomes in modulating disease vulnerability related to AD.


1961 ◽  
Vol 2 (1) ◽  
pp. 156-158 ◽  
Author(s):  
Bruce M. Cattanach

Welshons & Russell (1959) have presented data to show that the XO chromosomal constitution in the mouse is female. This conclusion was based on results of genetical tests with sex-linked markers and on chromosome counts. All XO females were matroclinous, that is, they had inherited their X-chromosome from their mother. Females of this type will arise when non-disjunction occurs in the meiotic divisions of the father and results in spermatozoa without a sex-chromosome. Alternatively, the paternal sex-chromosome may be lost from the fertilized ovum if non-disjunction of sister-chromatids occurs during the first cleavage division. This latter explanation has been urged by Ohno, Kaplan & Kinosita (1959), who found no evidence for non-disjunction of the X-and Y-chromosome in an extensive cytolosical examination of the mouse testis.


2019 ◽  
Author(s):  
Yehonatan Alcalay ◽  
Silke Fuchs ◽  
Roberto Galizi ◽  
Federica Bernardini ◽  
Roya Elaine Haghighat-Khah ◽  
...  

AbstractSynthetic sex-ratio distorters based on X-chromosome shredding are predicted to be more efficient than sterile males for population suppression of malaria mosquitoes using genetic control. X-chromosome shredding operates through the targeted elimination of X-chromosome-bearing gametes during male spermatogenesis, resulting in males that have a high fraction of male offspring. Strains harboring autosomal constructs containing a modified endonuclease I-PpoI have now been developed in the malaria mosquito Anopheles gambiae, resulting in strong sex-ratio distortion towards males. Data are being gathered for these strains for submission of regulatory dossiers for contained use and subsequent field release in West Africa. Since autosomal X-shredders are transmitted in a Mendelian fashion and can be selected against their frequency in the population is expected to decline once releases are halted. However, any unintended transfer of the X-shredder to the Y-chromosome could theoretically change these dynamics: This could lead to 100% transmission of the newly Y-linked X-shredder to the predominant male-biased offspring and its insulation from negative selection in females, resulting in its potential spread in the population and ultimately to suppression. Here, we analyze plausible mechanisms whereby an autosomal X-shredder could become linked to the Y-chromosome after release and provide data regarding its potential for activity should it become linked to the Y-chromosome. Our results strongly suggest that Y-chromosome linkage through remobilization of the transposon used for the initial genetic transformation is unlikely, and that, in the unexpected event that the X-shredder becomes linked to the Y-chromosome, expression and activity of the X-shredder would likely be inhibited by meiotic sex chromosome inactivation. We conclude that a functioning X-shredding-based Y-drive resulting from a naturally induced transposition or translocation of the transgene onto the Y-chromosome is unlikely.


2020 ◽  
Vol 12 (6) ◽  
pp. 965-977 ◽  
Author(s):  
Iulia Darolti ◽  
Alison E Wright ◽  
Judith E Mank

Abstract The loss of recombination triggers divergence between the sex chromosomes and promotes degeneration of the sex-limited chromosome. Several livebearers within the genus Poecilia share a male-heterogametic sex chromosome system that is roughly 20 Myr old, with extreme variation in the degree of Y chromosome divergence. In Poecilia picta, the Y is highly degenerate and associated with complete X chromosome dosage compensation. In contrast, although recombination is restricted across almost the entire length of the sex chromosomes in Poecilia reticulata and Poecilia wingei, divergence between the X chromosome and the Y chromosome is very low. This clade therefore offers a unique opportunity to study the forces that accelerate or hinder sex chromosome divergence. We used RNA-seq data from multiple families of both P. reticulata and P. wingei, the species with low levels of sex chromosome divergence, to differentiate X and Y coding sequences based on sex-limited SNP inheritance. Phylogenetic tree analyses reveal that occasional recombination has persisted between the sex chromosomes for much of their length, as X- and Y-linked sequences cluster by species instead of by gametolog. This incomplete recombination suppression maintains the extensive homomorphy observed in these systems. In addition, we see differences between the previously identified strata in the phylogenetic clustering of X–Y orthologs, with those that cluster by chromosome located in the older stratum, the region previously associated with the sex-determining locus. However, recombination arrest appears to have expanded throughout the sex chromosomes more gradually instead of through a stepwise process associated with inversions.


Development ◽  
1985 ◽  
Vol 88 (1) ◽  
pp. 327-332
Author(s):  
Heather Hogg ◽  
Anne Mclaren

Sex vesicles were not seen in meiotic germ cells isolated from male and female foetal adrenals, although they were readily identified in adult male meiotic germ cells prepared by the same air-drying method. It is suggested that the failure of the XY germ cells from the male adrenals to develop a sex vesicle is due to their embarking on oogenesis rather than spermatogenesis, and that the absence of a sex vesicle does not necessarily indicate lack of a Y chromosome.


PEDIATRICS ◽  
1995 ◽  
Vol 96 (6) ◽  
pp. 1166-1173
Author(s):  

This set of guidelines is designed to assist the pediatrician in caring for the child in whom the diagnosis of Turner syndrome has been confirmed by karyotype. Although the pediatrician's first contact with the child is usually during infancy, occasionally the pregnant woman who has been given the prenatal diagnosis of Turner syndrome will be referred for advice. Therefore, these guidelines offer advice for this situation as well. Turner syndrome, as used here, refers to a condition in which there is short stature and ovarian dysgenesis in females because of the absence of a normal second sex chromosome. Nonchrornosomal gonadal dysgenesis is excluded. The birth prevalence of Turner syndrome has been estimated to be from 1:2000 to 1:5000 female live births. About 1% to 2% of all conceptuses have a 45,X chromosome constitution. Of these, the majority (99%) spontaneously abort, usually during the first trimester of pregnancy. With the more frequent use of ultrasound, it is recognized that some pregnancies with a fetal 45,X chromosome constitution progressing into the second trimester are associated with nuchal cysts, severe lymphedema, or hydrops fetalis. These pregnancies are associated with a high frequency of fetal death. PHENOTYPE Pediatricians are most familiar with the clinical findings that prompt the diagnosis in children, namely, short stature and the classic Turner syndrome features such as lymphederna, webbed neck, low posterior hair line, and cubitus valgus. A wide range of clinical abnormalities may be found (Table 1). Turner syndrome, however, is not always accompanied by distinctive features and most often is not diagnosed in infancy.


2011 ◽  
Vol 96 (2) ◽  
pp. E356-E359 ◽  
Author(s):  
Sarina G. Kant ◽  
Hetty J. van der Kamp ◽  
Marjolein Kriek ◽  
Egbert Bakker ◽  
Boudewijn Bakker ◽  
...  

abstract Context: During meiosis I, the recombination frequency in the pseudoautosomal region on Xp and Yp (PAR1) in males is very high. As a result, mutated genes located within the PAR1 region can be transferred from the Y-chromosome to the X-chromosome and vice versa. Patients: Here we describe three families with SHOX abnormalities resulting in Leri-Weill dyschondrosteosis or Langer mesomelic dysplasia. Results: In about half of the segregations investigated, a transfer of the SHOX abnormality to the alternate sex chromosome was demonstrated. Conclusions: Patients with an abnormality of the SHOX gene should receive genetic counseling as to the likelihood that they may transmit the mutation or deletion to a son as well as to a daughter.


Genetics ◽  
2000 ◽  
Vol 156 (4) ◽  
pp. 1753-1763 ◽  
Author(s):  
Soojin Yi ◽  
Brian Charlesworth

Abstract In Drosophila miranda, a chromosome fusion between the Y chromosome and the autosome corresponding to Muller’s element C has created a new sex chromosome system. The chromosome attached to the ancestral Y chromosome is transmitted paternally and hence is not exposed to crossing over. This chromosome, conventionally called the neo-Y, and the homologous neo-X chromosome display many properties of evolving sex chromosomes. We report here the transposition of the exuperantia1 (exu1) locus from a neo-sex chromosome to the ancestral X chromosome of D. miranda. Exu1 is known to have several critical developmental functions, including a male-specific role in spermatogenesis. The ancestral location of exu1 is conserved in the sibling species of D. miranda, as well as in a more distantly related species. The transposition of exu1 can be interpreted as an adaptive fixation, driven by a selective advantage conferred by its effect on dosage compensation. This explanation is supported by the pattern of within-species sequence variation at exu1 and the nearby exu2 locus. The implications of this phenomenon for genome evolution are discussed.


The Lancet ◽  
1962 ◽  
Vol 280 (7245) ◽  
pp. 20-23 ◽  
Author(s):  
Leonard Atkins ◽  
Eric Engel ◽  
DAVIDA. Flory ◽  
Mireille Engel

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