Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man

1991 ◽  
Vol 87 (4) ◽  
Author(s):  
R.M. Speed ◽  
M.J.W. Faed ◽  
P.J. Batstone ◽  
K. Baxby ◽  
W. Barnetson
Keyword(s):  
Meiotic Prophase ◽  
Y Chromosomes ◽  
Metaphase I

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.

scholarly journals Meiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1β and SMC3

2003 ◽  
Vol 160 (5) ◽  
pp. 657-670 ◽  
Author(s):  
Maureen Eijpe ◽  
Hildo Offenberg ◽  
Rolf Jessberger ◽  
Ekaterina Revenkova ◽  
Christa Heyting
Keyword(s):  
Synaptonemal Complex ◽  
Sister Chromatid ◽  
Meiotic Prophase ◽  
S Phase ◽  
Synaptonemal Complexes ◽  
Sister Chromatids ◽  
Chromatid Cohesion ◽  
Axial Element ◽  
Striking Contrast ◽  
Metaphase I

In meiotic prophase, the sister chromatids of each chromosome develop a common axial element (AE) that is integrated into the synaptonemal complex (SC). We analyzed the incorporation of sister chromatid cohesion proteins (cohesins) and other AE components into AEs. Meiotic cohesin REC8 appeared shortly before premeiotic S phase in the nucleus and formed AE-like structures (REC8-AEs) from premeiotic S phase on. Subsequently, meiotic cohesin SMC1β, cohesin SMC3, and AE proteins SCP2 and SCP3 formed dots along REC8-AEs, which extended and fused until they lined REC8-AEs along their length. In metaphase I, SMC1β, SMC3, SCP2, and SCP3 disappeared from the chromosome arms and accumulated around the centromeres, where they stayed until anaphase II. In striking contrast, REC8 persisted along the chromosome arms until anaphase I and near the centromeres until anaphase II. We propose that REC8 provides a basis for AE formation and that the first steps in AE assembly do not require SMC1β, SMC3, SCP2, and SCP3. Furthermore, SMC1β, SMC3, SCP2, and SCP3 cannot provide arm cohesion during metaphase I. We propose that REC8 then provides cohesion. RAD51 and/or DMC1 coimmunoprecipitates with REC8, suggesting that REC8 may also provide a basis for assembly of recombination complexes.

Chromosomal synapsis and the meiotic process in male mesquite lizards, Sceloporus grammicus complex

Genome ◽  
1992 ◽  
Vol 35 (3) ◽  
pp. 398-408 ◽  
Author(s):  
Kent M. Reed ◽  
Jack W. Sites Jr. ◽  
Ira F. Greenbaum
Keyword(s):  
Synaptonemal Complex ◽  
Sex Chromosomes ◽  
Meiotic Prophase ◽  
Morphological Characterization ◽  
Autosomal Bivalents ◽  
Meiotic Process ◽  
Low Levels ◽  
Sceloporus Grammicus ◽  
Metaphase I

Meiosis in males of the F5 cytotype of Sceloporus grammicus was examined through the analysis of synaptonemal complexes (SCs), diakinetic (metaphase I) nuclei, and secondary spermatocytes (metaphase II configurations). These data allowed the establishment of criteria for substaging of zygonema and pachynema, morphological characterization of the SC complement, and comparison of the orientation and segregation of the autosomes and sex chromosomes. The analysis of nuclei from all stages of meiotic prophase I (leptonema through diakinesis) provided a useful means of partitioning the temporal sequence of early meiotic events. Three substages of zygonema (Z1–Z3) were established, based on the extent of synapsis of the microchromosomal and macrochromosomal elements. Synaptic initiation of the autosomes and sex chromosomes was synchronous. Two patterns of macrochromosomal synapsis were observed. Whereas synapsis of the biarmed elements was biterminal (i.e., progressing from both ends of the homologs), synapsis of the acrocentric elements was uniterminal involving only the distal (noncentromeric) ends of the homologs. Unique sex-chromosomal characteristics were not observed in S. grammicus and, therefore, the substaging of pachynema was based on subjective criteria. Examination of diakinesis – metaphase I and metaphase II configurations indicated low levels of diakinetic irregularities with balanced segregation of the autosomal bivalents and the sex-chromosomal trivalent.Key words: Sceloporus grammicus, meiosis, synaptonemal complex, substaging.

Morphological and temporal sequence of meiotic prophase development at puberty in the male mouse

1984 ◽  
Vol 65 (1) ◽  
pp. 249-263
Author(s):  
P. Goetz ◽  
A.C. Chandley ◽  
R.M. Speed
Keyword(s):  
Synaptonemal Complex ◽  
Adult Male ◽  
Meiotic Prophase ◽  
Male Mouse ◽  
Late Pachytene ◽  
Diplotene Stage ◽  
Y Chromosomes ◽  
Correct Sequence ◽  
Xy Bivalent ◽  
Morphological Detail

The correct sequence of meiotic prophase development in the male mouse has been established by the use of pubertal males. The first wave of spermatogenesis at this time provides a unique opportunity to study progressive meiotic development in a direct way. Air-dried and micro-spread analyses have been carried out. Temporal and morphological progression at this time is entirely consistent with that occurring in the later waves of meiosis of the adult male. Morphological detail shows delayed pairing of the X and Y chromosomes relative to the autosomes. The longest XY synaptonemal complex is seen in early pachytene cells, occupying up to 72% of the length of the Y and 22% of the length of the X axis. By late pachytene, end-to-end pairing in the XY bivalent is established, the autosomal axes remaining fully paired. Desynapsis of the autosomes commences at early diplotene. A ‘diffuse’ diplotene stage in the male, comparable to the dictyate stage of the female, could not be found. Marked lengthening of the XY and autosomal axes did, however, occur through the diplotene stage.

scholarly journals SKP1 drives the prophase I to metaphase I transition during male meiosis

2020 ◽  
Vol 6 (13) ◽  
pp. eaaz2129 ◽  
Author(s):  
Yongjuan Guan ◽  
N. Adrian Leu ◽  
Jun Ma ◽  
Lukáš Chmátal ◽  
Gordon Ruthel ◽  
...  
Keyword(s):  
Okadaic Acid ◽  
Meiotic Prophase ◽  
Essential Role ◽  
Male Meiosis ◽  
Prophase I ◽  
Ubiquitin E3 Ligase ◽  
Competence Factor ◽  
Competence Acquisition ◽  
Mi Transition ◽  
Metaphase I

The meiotic prophase I to metaphase I (PI/MI) transition requires chromosome desynapsis and metaphase competence acquisition. However, control of these major meiotic events is poorly understood. Here, we identify an essential role for SKP1, a core subunit of the SKP1–Cullin–F-box (SCF) ubiquitin E3 ligase, in the PI/MI transition. SKP1 localizes to synapsed chromosome axes and evicts HORMAD proteins from these regions in meiotic spermatocytes. SKP1-deficient spermatocytes display premature desynapsis, precocious pachytene exit, loss of PLK1 and BUB1 at centromeres, but persistence of HORMAD, γH2AX, RPA2, and MLH1 in diplonema. Strikingly, SKP1-deficient spermatocytes show sharply reduced MPF activity and fail to enter MI despite treatment with okadaic acid. SKP1-deficient oocytes exhibit desynapsis, chromosome misalignment, and progressive postnatal loss. Therefore, SKP1 maintains synapsis in meiosis of both sexes. Furthermore, our results support a model where SKP1 functions as the long-sought intrinsic metaphase competence factor to orchestrate MI entry during male meiosis.

scholarly journals The behavior of the X- and Y-chromosomes in the oocyte during meiotic prophase in the B6.YTIR sex-reversed mouse ovary

Reproduction ◽  
2008 ◽  
Vol 135 (2) ◽  
pp. 241-252 ◽  
Author(s):  
Michelle Alton ◽  
Mau Pan Lau ◽  
Michele Villemure ◽  
Teruko Taketo
Keyword(s):  
Y Chromosome ◽  
Germ Cells ◽  
Sex Chromosomes ◽  
Meiotic Prophase ◽  
Transcriptional Repression ◽  
Transcriptional Activity ◽  
Sex Chromosome ◽  
Nuclear Antigen ◽  
Mouse Ovary ◽  
Y Chromosomes

Sexual differentiation of the germ cells follows gonadal differentiation, which is determined by the presence or the absence of the Y-chromosome. Consequently, oogenesis and spermatogenesis take place in the germ cells with XX and XY sex chromosomal compositions respectively. It is unclear how sexual dimorphic regulation of meiosis is associated with the sex-chromosomal composition. In the present study, we examined the behavior of the sex chromosomes in the oocytes of the B6.YTIRsex-reversed female mouse, in comparison with XO and XX females. As the sex chromosomes fail to pair in both XY and XO oocytes during meiotic prophase, we anticipated that the pairing failure may lead to excessive oocyte loss. However, the total number of germ cells, identified by immunolabeling of germ cell nuclear antigen 1 (GCNA1), did not differ between XY and XX ovaries or XO and XX ovaries up to the day of delivery. The progression of meiotic prophase, assessed by immunolabeling of synaptonemal complex components, was also similar between the two genotypes of ovaries. These observations suggest that the failure in sex-chromosome pairing is not sufficient to cause oocyte loss. On the other hand, labeling of phosphorylated histone γH2AX, known to be associated with asynapsis and transcriptional repression, was seen over the X-chromosome but not over the Y-chromosome in the majority of XY oocytes at the pachytene stage. For comparison, γH2AX labeling was seen only in the minority of XX oocytes at the same stage. We speculate that the transcriptional activity of sex chromosomes in the XY oocyte may be incompatible with ooplasmic maturation.

scholarly journals Regulation of the meiotic prophase I to metaphase I transition in mouse spermatocytes

Chromosoma ◽  
2008 ◽  
Vol 117 (5) ◽  
pp. 471-485 ◽  
Author(s):  
Fengyun Sun ◽  
Mary Ann Handel
Keyword(s):  
Meiotic Prophase ◽  
Prophase I ◽  
Meiotic Prophase I ◽  
Metaphase I

Sequential meiotic prophase development in the pubertal Indian pygmy field mouse: Synaptic progression of the XY chromosomes, autosomal heterochromatin, and pericentric inversions

Genome ◽  
2000 ◽  
Vol 43 (1) ◽  
pp. 172-180 ◽  
Author(s):  
Amit Bardhan ◽  
T Sharma
Keyword(s):  
Meiotic Prophase ◽  
Pericentric Inversion ◽  
Chiasma Formation ◽  
Subsequent Paper ◽  
Y Chromosomes ◽  
Xy Bivalent ◽  
Mus Terricolor ◽  
Chromosomal Changes ◽  
Meiotic Synapsis ◽  
Chromosomal Mutations

Sequential meiotic prophase development has been followed in the pubertal male pygmy mouse Mus terricolor, with the objective to identify early meiotic prophase stages. The pygmy mouse differs from the common mouse by having large heterochromatic blocks in the X and Y chromosomes. These mice also show various chromosomal mutations; for example, fixed variations of autosomal short arms heterochromatin among different chromosomal species and pericentric inversion polymorphism. Identification of prophase stages was crucial to analyzing effects of heterozygosity for these chromosomal changes on the process of homologous synapsis. Here we describe identification of the prophase stages in M. terricolor, especially the pachytene substages, on the basis of morphology of the XY bivalent. Based on this substaging, we show delayed pairing of the heterochromatic short arms, which may be the reason for their lack of chiasmata. The identification of precise pachytene substages also reveals an early occurrence of "synaptic adjustment" in the pericentric inversion heterobivalents, a mechanism that would prevent chiasma formation in the inverted segment and thereby would abate adverse effects of such heterozygosity. The identification of pachytene substages would serve as the basis to analyze the nature of synaptic anomalies met in M. terricolor hybrids (which will be the basis of a subsequent paper). Key words: Mus terricolor, meiotic synapsis, sex chromosomes, pericentric inversion, heterochromatin.

scholarly journals Silencing of Unpaired Chromatin and Histone H2A Ubiquitination in Mammalian Meiosis

2005 ◽  
Vol 25 (3) ◽  
pp. 1041-1053 ◽  
Author(s):  
Willy M. Baarends ◽  
Evelyne Wassenaar ◽  
Roald van der Laan ◽  
Jos Hoogerbrugge ◽  
Esther Sleddens-Linkels ◽  
...  
Keyword(s):  
Mouse Models ◽  
Meiotic Prophase ◽  
Transcriptional Silencing ◽  
Male Meiosis ◽  
Histone H2a ◽  
Barr Body ◽  
Female Meiosis ◽  
Autosomal Region ◽  
Y Chromosomes ◽  
The Relationship

ABSTRACT During meiotic prophase in male mammals, the X and Y chromosomes are incorporated in the XY body. This heterochromatic body is transcriptionally silenced and marked by increased ubiquitination of histone H2A. This led us to investigate the relationship between histone H2A ubiquitination and chromatin silencing in more detail. First, we found that ubiquitinated H2A also marks the silenced X chromosome of the Barr body in female somatic cells. Next, we studied a possible relationship between H2A ubiquitination, chromatin silencing, and unpaired chromatin in meiotic prophase. The mouse models used carry an unpaired autosomal region in male meiosis or unpaired X and Y chromosomes in female meiosis. We show that ubiquitinated histone H2A is associated with transcriptional silencing of large chromatin regions. This silencing in mammalian meiotic prophase cells concerns unpaired chromatin regions and resembles a phenomenon described for the fungus Neurospora crassa and named meiotic silencing by unpaired DNA.

scholarly journals Analysis of the synaptonemal complex of the nine-banded armadillo, Dasypus novemcinctus

2000 ◽  
Vol 23 (3) ◽  
pp. 613-616 ◽  
Author(s):  
Márcia Denise da Paixão Scavone ◽  
Claudio Oliveira ◽  
Eduardo Bagagli ◽  
Fausto Foresti
Keyword(s):  
Synaptonemal Complex ◽  
Meiotic Prophase ◽  
Dasypus Novemcinctus ◽  
Late Pachytene ◽  
Chromosome Synapsis ◽  
Structure Changes ◽  
Y Chromosomes ◽  
Bivalent Chromosome ◽  
In Cells

The synaptonemal complex (SC) of three specimens of the nine-banded armadillo (Dasypus novemcinctus) was analyzed. Thirty-two bivalents (2n = 64) were observed, 31 of them being autosomes and one an XY sexual bivalent. Chromosome synapsis processes and nucleolus structure changes were analyzed in zygotene and pachytene cells, allowing a detailed description of the beginning of meiotic prophase in this species. There was complete synapsis of X and Y chromosomes. Some abnormalities in SC were observed in cells during zygotene and at the beginning of pachytene, but not in cells in the middle and late pachytene, suggesting the occurrence of synaptic adjustments in their SC.

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