The frequency of chromosome segregation errors during meiosis I (MI) in oocytes increases with age. The two-hit model suggests that errors are caused by the combination of a first hit that creates susceptible crossover configurations and a second hit comprising an age-related reduction in chromosome cohesion. This model predicts an age-related increase in univalents, but direct evidence of this phenomenon as a major cause of segregation errors has been lacking. Here, we provide the first live analysis of single chromosomes undergoing segregation errors during MI in the oocytes of naturally aged mice. Chromosome tracking reveals that 80% of the errors are preceded by bivalent separation into univalents. The set of the univalents is biased towards balanced and unbalanced predivision of sister chromatids during MI. Moreover, we find univalents predisposed to predivision in human oocytes. This study defines premature bivalent separation into univalents as the primary defect responsible for age-related aneuploidy.
Aneuploidy is a leading cause of miscarriage and congenital diseases such as Down syndrome. Most aneuploid chromosomes originate from segregation errors during meiosis I (MI) in oocytes, and the frequency of the errors increases with age1,2,3,4. The two-hit model suggests that segregation errors during MI are caused by the combination of a first hit that creates susceptible crossover configurations during the foetal stage and a second hit comprising an age-related reduction in chromosome cohesion during the dictyate stage1,5,6,7,8. One prediction of this model is the existence of an age-related increase in univalents. Consistent with this prediction, Smc1b knockout oocytes, which have a reduced amount of cohesin, exhibit an age-related increase in univalents9. However, direct evidence of univalents as a major cause of segregation errors in the oocytes of naturally aged animals has been lacking10,11,12,13,14,15. Although an age-related increase in univalents in the oocytes of naturally aged mice was first suggested over four decades ago16, it was argued that most, if not all, of the univalents observed in that study were artefacts of chromosome spread10,11,12. Recent studies found univalents in a very small fraction of the oocytes of naturally aged mice13,14, which seemed unlikely to account for the majority of chromosome segregation errors during MI. These and other studies found weakly associated bivalents in a significant fraction of the oocytes of naturally aged mice13,14,15, but these bivalents undergo normal segregation during MI13. Instead, available evidence from naturally aged mice led to the proposal that an age-related reduction in cohesion between sister kinetochores (KTs)14,15 and defects in KT–microtubule interaction17 are leading causes of segregation errors during MI. Thus, the actual cause of segregation errors during MI in the oocytes of naturally aged animals remains unclear.
Here, we provide direct evidence that premature bivalent separation into univalents is the major cause of chromosome segregation errors during MI. By using high-resolution and high-throughput live imaging microscopy and complete three-dimensional (3D) tracking of KTs in the oocytes of naturally aged mice, we show that the vast majority of chromosome segregation errors are preceded by bivalent hyperstretching and subsequent separation into univalents. The univalents are strongly biased towards predivision of sister chromatids. We provide direct observation of balanced predivision of sister chromatids during MI, which was hypothesized two decades ago5, as a major type of age-related chromosome segregation errors. Consistent with observations in mouse oocytes, human oocytes exhibit univalents that are predisposed to predivision of sister chromatids during MI.
Direct observation of age-related MI errors
There are potentially three distinct types of segregation errors during MI: nondisjunction of homologous chromosomes (4:0 segregation), unbalanced predivision of sister chromatids (3:1 segregation) and balanced predivision of sister chromatids (2:2 segregation) (Supplementary Fig. 1). Balanced predivision5, in which both homologous chromosomes undergo sister chromatid segregation during MI, has not yet been directly demonstrated because it is indistinguishable from premature sister chromatid separation during meiosis II (MII) by conventional approaches using fixed metaphase II oocytes. To directly observe chromosome segregation errors, we established a high-resolution and high-throughput imaging of KTs and chromosomes in live mouse oocytes (Fig. 1a and Supplementary Movie 1)18. We generated four-dimensional data sets throughout MI for 275 ‘aged’ oocytes obtained from 16-month-old BDF1 mice and for 167 ‘young’ oocytes obtained from 2-month-old mice (Supplementary Table 1). The data sets allowed us to robustly track all KTs in 3D from prometaphase to anaphase I (Fig. 1a, Supplementary Movie 2)18. Manual assessment of all KT trajectories during anaphase I (Fig. 1b) indicated that 20/275 aged oocytes (7.3%) underwent segregation errors during MI, whereas no young oocytes did (0/167; Fig. 1c and Supplementary Table 1). This KT tracking analysis revealed that balanced predivision of sister chromatids (9/20, 45%) and unbalanced predivision of sister chromatids (7/20, 35%) are predominant over nondisjunction of homologous chromosomes (4/20, 20%) (Fig. 1c). Similar results were obtained for oocytes from aged CD-1 mice (7/13, 54% balanced predivision; 3/13, 23% unbalanced predivision; and 3/13, 23% nondisjunction) (Fig. 1c). Counting the number of KTs in aged BDF1 oocytes fixed at metaphase II suggested that live imaging had no adverse effect on the rates of unbalanced predivision and nondisjunction (Supplementary Fig. 2 and Supplementary Movie 3). These results indicate that segregation errors during MI are strongly biased towards predivision of sister chromatids, including balanced predivision.
Bivalent separation into univalents precedes MI errors
Strikingly, analysis of the KT trajectories of the chromosomes later associated with segregation errors suggested premature bivalent separation (Supplementary Movie 4). Hereafter, we refer to these chromosomes as ‘S-chromosomes’. Before metaphase I, an S-chromosome appeared as a normal bivalent with a pair of homologous KTs (Fig. 2a(i)). Upon entry into metaphase I, the S-chromosome bivalent stretched with a similar timing to that of the other bivalents (Fig. 2a–c(ii)). This stretching resulted in an extremely long distance between the homologous KTs (inter-homologous KT distance; Fig. 2a,c(iii)). Although no detectable H2B-mCherry signal was observed in the middle of the hyperstretched bivalent (Fig. 2a(iii)), it was possible that the homologous chromosomes were still functionally connected because the line connecting the homologous KTs (inter-homologous KT axis) was stably oriented along the spindle axis for a maximum of 233 min (Fig. 2b,d and Supplementary Fig. 3). This observation of hyperstretched bivalents is consistent with a previous report13. Thereafter, however, we found that the homologous KTs of the S-chromosome suddenly began to oscillate independently between the spindle poles at an increased speed (Fig. 2a–e(iv) and Supplementary Movie 4). The characteristic profiles of this oscillation were indistinguishable from those of univalents generated due to a defect in synaptonemal complex formation in the oocytes of young Sycp3 knockout mice (Supplementary Fig. 4 and Supplementary Movie 5)19. We therefore functionally define these apparently separated S-chromosome units exhibiting independent oscillation as univalents. Importantly, of the 20 chromosomes that exhibited segregation errors during MI in aged BDF1 oocytes, 16 (80%) showed bivalent hyperstretching followed by separation into univalents (Fig. 2f, Supplementary Fig. 3 and Supplementary Table 1). The same phenomenon preceded 85% (11/13) of segregation errors during MI in oocytes from aged CD-1 mice (Fig. 2f and Supplementary Fig. 5). These results suggest that premature bivalent separation into univalents precedes the majority of chromosome segregation errors during MI in the oocytes of aged mice.
Age-related increase in univalents in mouse oocytes
To confirm the age-related increase in univalents, we fixed and immunostained oocytes at late metaphase I without chromosome spreading. Determination of all KT positions in 3D revealed that a significant fraction of aged oocytes had univalents, whereas no young oocytes did (Fig. 3a–c and Supplementary Movie 6). The rate of univalents remained consistent between fixed and live oocytes (Fig. 3c). The sister KTs of these univalents were frequently bioriented and aligned on the metaphase plate (Fig. 3b,d,e), which was consistent with the observation of univalents that later exhibited sister chromatid predivision in live aged oocytes (Supplementary Fig. 6). These results confirm the age-related increase in univalents as the major cause of segregation errors during MI in mouse oocytes.
Univalents in human oocytes
To investigate whether univalents are observed in human oocytes, we fixed and immunostained oocytes at MI from patients of different ages without chromosome spreading. Determination of all KT positions in 3D (Fig. 4a and Supplementary Movie 7) revealed that among 16 oocytes carrying a metaphase plate, three oocytes from relatively old patients contained univalents (Fig. 4b,c and Supplementary Movie 8). The sister KTs of the univalents were frequently bioriented and aligned on the metaphase plate (Fig. 4b,d,e), which suggests a predisposition to sister chromatid predivision during MI. On bivalents, the inter-sister KT distance was significantly greater in oocytes from older patients (Fig. 4d), as observed in mouse oocytes (Fig. 3d)14,15. This age-related reduction in sister KT cohesion had a significant but relatively small impact on the capacity of bivalents to biorient the homologous KTs (Fig. 4f) and to monoorient the sister KTs (Fig. 4e), whereas univalent formation strongly biased towards biorientation of the sister KTs (Fig. 4e). These results suggest that univalent formation, presumably through premature bivalent separation as observed in mouse oocytes, is a critical event for chromosome segregation errors during MI in human oocytes.
It has long been speculated that an age-related increase in univalents might be a leading cause of chromosome segregation errors in oocytes5,6,7,9,16,19. In 1968, Henderson and Edwards16 observed an age-related increase in univalents in chromosome spread samples of the oocytes from naturally aged mice. Recent studies detected univalents in the oocytes from naturally aged mice without chromosome spreading13,14, although the sample size in these studies was insufficient to show statistical significance and the rate of the detected univalents did not match the rate of chromosome segregation errors. Instead, these and other studies observed a significant age-related increase in weakly associated bivalents and sister KTs13,14,15, raising the possibility that these defects are a leading cause of chromosome segregation errors.
In the present study, our systematic analyses of the dynamics and structures of single chromosomes in the oocytes of naturally aged mice provided direct evidence that premature bivalent separation into univalents is the major cause of age-related chromosome segregation errors during MI (Fig. 5). Consistent with this finding, we observed univalents predisposed to segregation errors in human oocytes, although this observation should be interpreted cautiously because oocytes that remained immature after hormonal stimulation were used in this study. In mouse oocytes, a small fraction of segregation errors were not preceded by premature bivalent separation (4/20, 20% in BDF1; 2/13, 15% in CD-1; Supplementary Table 1). Future studies are needed to determine whether these errors are attributed to an age-related loss of sister KT cohesion on intact bivalents14,15 or other defects that facilitate incorrect KT–microtubule attachments17.
Our observation of premature bivalent separation into univalents is consistent with a prediction of the two-hit model1,5,6,7,8. Our findings suggest that the functional connection between the homologous chromosomes of bivalents subjected to both hits is resolved by microtubule-mediated forces for bivalent stretching, which thus results in production of univalents (Fig. 5). The possibility that a leak of separase activity contributed to the bivalent separation cannot be excluded. The sister KTs of the univalents are strongly biased towards bipolar microtubule attachment, possibly for two reasons. First, monopolar microtubule attachments to the sister KTs fail to be stabilized due to a loss of tension between homologous KTs, whereas bipolar attachments can be stabilized by the tension between sister KTs19,20. Second, an age-related loss of sister KT cohesion14,15 may disrupt MI-specific sister KT geometry that is known to be essential for univalents, but largely dispensable for bivalents, to make monopolar microtubule attachments to the sister KTs21,22.
Consequently, the set of the univalents frequently results in balanced and unbalanced predivision of sister chromatids during MI (Fig. 5). Unbalanced predivision is consistent with the aneuploidy observed in human metaphase II oocytes5,7,23,24,25,26,27. Furthermore, balanced predivision, which was demonstrated to be the most predominant type of segregation errors during MI in mouse oocytes in this study, may reconcile the available human data. DNA polymorphism analyses of human trisomies have shown that most aneuploid chromosomes are caused by segregation errors during MI1,2,3,4, whereas genome-based DNA analyses of human oocytes reveal that chromosome number abnormalities are more frequent after MII than after MI25,28. This apparent discrepancy can be reconciled by balanced predivision during MI, which results in the normal number of chromatids after MI but a predisposition to an abnormal number after MII. Taking these findings together, we suggest that premature bivalent separation into univalents is a predominant cause of age-related segregation errors during MI in human oocytes. This study provides a basis for the development of strategies to prevent age-related production of aneuploid eggs, such as the introduction of an artificial tie that could physically secure homologous chromosomes until the onset of anaphase I in maturing oocytes.
Oocyte culture and microinjection of mRNA
Two- or 16-month-old BDF1, 11-month-old CD-1 and 2-month-old Sycp3−/− (in C57BL/6 background) female mice were primed with an injection of pregnant mare’s serum gonadotropin (Serotoropin, ASKA Pharmaceutical). Ovaries were excised and oocytes at the germinal vesicle stage were collected. The collected oocytes were cultured in M2 medium supplemented with 200 nM 3-isobutyl-1-metyl-xanthine (IBMX, Sigma). In vitro-transcribed mRNAs (1.2 pl of 650 ng μl−1 2mEGFP-CENP-C and 0.6 pl of 350 ng μl−1 H2B-mCherry) were microinjected into oocytes. The microinjected oocytes were cultured for 2.5−3.0 h and then released to undergo meiotic maturation through the removal of IBMX from the culture. Oocytes that expressed a moderate level of H2B-mCherry at the germinal vesicle stage were used for further analysis. All experiments involving mice were approved (AH26-04) and carried out under the guidelines of RIKEN CDB.
Time-lapse imaging data acquisition
Time-lapse imaging was performed as previously described18 with some modifications. Briefly, a Zeiss LSM710 confocal microscope equipped with a 40 × C-Apochromat 1.2NA water immersion objective lens (Carl Zeiss) was controlled by a multi-position autofocus macro29, which allowed us to record a maximum 32 oocytes in one experiment. Seventeen confocal z-sections (every 1.5 μm) of 256 × 256 pixel xy images covering a total volume of 30.4 × 30.4 × 25.5 μm were acquired at 3-min intervals for at least 12 h after inducing a resumption of meiosis. The KT signals were peak-enhanced and background-subtracted as previously described18.
KT tracking was performed as previously described18. The distance between homologous KTs (inter-homologous KT distance) at 15 min before the onset of anaphase I was defined as the final inter-homologous KT distance. The inter-homologous KT distance at each time point was normalized to the final inter-homologous KT distance. Metaphase entry was defined as the time when >50% of bivalents maintained a minimum inter-homologous KT distance that exceeded 70% for three consecutive time points. Once the inter-homologous KT distance of a bivalent has exceeded 12 μm, this bivalent was defined as hyperstretched. Once the homologous KTs of a bivalent initiated independent oscillation, this bivalent was defined as separated into univalents.
The centre of the spindle was defined as the centre of mass of all KT positions. The orientation of the spindle axis was defined as the average orientation of the inter-homologous KT axes of bivalents showing an inter-homologous KT distance >70%. The KT positions of univalents were eliminated from the calculations of the centre and axis of the spindle. The plane orthogonal to the spindle axis and passing through the spindle centre was defined as the spindle equator. The spindle equator at the time of metaphase entry was used for all time points before the metaphase entry.
To measure the oscillation amplitude, oscillation frequency and KT speed, the KT tracks were fitted with a cubic smoothing spline. The initiation of independent movements of separated chromosome units was defined as the point at which the KT began to exhibit consecutive anti-poleward movement over three time points, followed by a displacement of over 10 μm within 15 min. The time point when a KT began to exhibit consecutive poleward or anti-poleward movement over three time points was defined as the turning point. The oscillation amplitude was defined as the KT displacement along the spindle axis from a turning point to the next. The oscillation frequency was defined as the number of turning points after a KT displacement over 10 μm.
Immunostaining of mouse oocytes
Oocytes that underwent nuclear envelope breakdown (NEBD) within 60 min after the induction of meiotic resumption were collected either 6 h after NEBD (late metaphase I) or 12–14 h after NEBD (metaphase II). The oocytes were fixed with 1.6% paraformaldehyde in 100 mM PIPES pH 7.0, 1 mM MgCl2 and 0.1% Triton X-100 for 30 min at room temperature. The fixed oocytes were washed three times with PBT (0.1% Triton X-100 in PBS) and then blocked with 3% BSA–PBT at 4 °C overnight. The oocytes were then incubated with human anti-centromere antibodies (ACA, Antibodies Incorporated, 15-234) at 1:100 in 3% BSA–PBT at 4 °C overnight. The oocytes were subsequently washed three times with 3% BSA–PBT and incubated with an Alexa Fluor 488 goat anti-human antibody (Molecular Probes, A11013) at 1:500 in 3% BSA–PBT at room temperature for 4 h in the dark. DNA was counterstained with 40 μg ml−1 Hoechst 33342. The oocytes were finally washed again and transferred to 0.01% BSA–PBS for imaging with a Zeiss LSM780 confocal microscope. Confocal z-sections (every 0.2 μm) of 512 × 512 pixel xy images covering the total volume of the spindle were acquired. The images were reconstructed into 3D with Imaris software (Bitplane).
Human oocyte experiments
Human oocyte experiments were approved by institutional human research ethics committees at RIKEN (KOBE-IRB-13-22) and IVF Namba Clinic (2014-1), registered in Japan Society of Obstetrics and Gynecology (registry number 132), and carried out under these guidelines. Immature oocytes that were not used for fertility treatment were donated after patients received a full explanation of the experiments and provided signed informed consent.
Controlled ovarian stimulation was performed by using standard protocols with modifications according to the patients’ medical history. Oocytes were picked up by transvaginal aspiration with an 18 gauge single lumen needle (Smiths Medical) 36 h after human chorionic gonadotropin injection. All mature oocytes were inseminated by intracytoplasmic sperm injection for fertility treatment. Oocytes that were still immature at 42 h after human chorionic gonadotropin injection were donated for this study. The immature oocytes were fixed in 2% paraformaldehyde solution at 37 °C for 30 min. Immunostaining was performed by the same procedure that was used for mouse oocytes except for primary antibody incubation for two overnights. The oocytes were imaged with a Zeiss LSM780 confocal microscope equipped with a 63 × C-Apochromat 1.2NA water immersion objective lens. To remove oocytes that were degenerate or otherwise aberrant, we selected oocytes that exhibit a metaphase plate with or without misaligned chromosomes for high-resolution imaging. Confocal z-sections (every 0.2 μm) of 512 × 512 pixel xy images covering the total volume of the spindle were acquired. The images were reconstructed into 3D with Imaris software.
How to cite this article: Sakakibara, Y. et al. Bivalent separation into univalents precedes age-related meiosis I errors in oocytes. Nat. Commun. 6:7550 doi: 10.1038/ncomms8550 (2015).
Hassold, T. & Sherman, S. Down syndrome: genetic recombination and the origin of the extra chromosome 21. Clin. Genet. 57, 95–100 (2000).
Chiang, T., Schultz, R. M. & Lampson, M. A. Meiotic origins of maternal age-related aneuploidy. Biol. Reprod. 86, 1–7 (2012).
Nagaoka, S. I., Hassold, T. J. & Hunt, P. A. Human aneuploidy: mechanisms and new insights into an age-old problem. Nat. Rev. Genet. 13, 493–504 (2012).
Jones, K. T. & Lane, S. I. Molecular causes of aneuploidy in mammalian eggs. Development 140, 3719–3730 (2013).
Angell, R. R. Predivision in human oocytes at meiosis I: a mechanism for trisomy formation in man. Hum. Genet. 86, 383–387 (1991).
Lamb, N. E. et al. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat. Genet. 14, 400–405 (1996).
Angell, R. First-meiotic-division nondisjunction in human oocytes. Am. J. Hum. Genet. 61, 23–32 (1997).
Jessberger, R. Age-related aneuploidy through cohesion exhaustion. EMBO Rep. 13, 539–546 (2012).
Hodges, C. A., Revenkova, E., Jessberger, R., Hassold, T. J. & Hunt, P. A. SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction. Nat. Genet. 37, 1351–1355 (2005).
Polani, P. E. & Jagiello, G. M. Chiasmata, meiotic univalents, and age in relation to aneuploid imbalance in mice. Cytogenet. Cell Genet. 16, 505–529 (1976).
Speed, R. M. The effects of ageing on the meiotic chromosomes of male and female mice. Chromosoma 64, 241–254 (1977).
Sugawara, S. & Mikamo, K. Maternal ageing and nondisjunction: a comparative study of two chromosomal techniques on the formation of univalents in first meiotic metaphase oocytes of the mouse. Chromosoma 93, 321–325 (1986).
Yun, Y., Lane, S. I. & Jones, K. T. Premature dyad separation in meiosis II is the major segregation error with maternal age in mouse oocytes. Development 141, 199–208 (2014).
Chiang, T., Duncan, F. E., Schindler, K., Schultz, R. M. & Lampson, M. A. Evidence that weakened centromere cohesion is a leading cause of age-related aneuploidy in oocytes. Curr. Biol. 20, 1522–1528 (2010).
Lister, L. M. et al. Age-related meiotic segregation errors in mammalian oocytes are preceded by depletion of cohesin and Sgo2. Curr. Biol. 20, 1511–1521 (2010).
Henderson, S. & Edwards, R. Chiasma frequency and maternal age in mammals. Nature 218, 22–28 (1968).
Shomper, M., Lappa, C. & FitzHarris, G. Kinetochore microtubule establishment is defective in oocytes from aged mice. Cell Cycle 13, 1171–1179 (2014).
Kitajima, T. S., Ohsugi, M. & Ellenberg, J. Complete kinetochore tracking reveals error-prone homologous chromosome biorientation in mammalian oocytes. Cell 146, 568–581 (2011).
Kouznetsova, A., Lister, L., Nordenskjöld, M., Herbert, M. & Höög, C. Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in mice. Nat. Genet. 39, 966–968 (2007).
LeMaire-Adkins, R., Radke, K. & Hunt, P. A. Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females. J. Cell Biol. 139, 1611–1619 (1997).
Sakuno, T., Tada, K. & Watanabe, Y. Kinetochore geometry defined by cohesion within the centromere. Nature 458, 852–858 (2009).
Kim, J. et al. Meikin is a conserved regulator of meiosis-I-specific kinetochore function. Nature 517, 466–471 (2015).
Vialard, F. et al. Evidence of a high proportion of premature unbalanced separation of sister chromatids in the first polar bodies of women of advanced age. Hum. Reprod. 21, 1172–1178 (2006).
Gabriel, A. S. et al. Array comparative genomic hybridisation on first polar bodies suggests that non-disjunction is not the predominant mechanism leading to aneuploidy in humans. J. Med. Genet. 48, 433–437 (2011).
Handyside, A. H. et al. Multiple meiotic errors caused by predivision of chromatids in women of advanced maternal age undergoing in vitro fertilisation. Eur. J. Hum. Genet. 20, 742–747 (2012).
Forman, E. J. et al. Embryos whose polar bodies contain isolated reciprocal chromosome aneuploidy are almost always euploid. Hum. Reprod. 28, 502–508 (2013).
Pellestor, F., Andréo, B., Arnal, F., Humeau, C. & Demaille, J. Mechanisms of non-disjunction in human female meiosis: the co-existence of two modes of malsegregation evidenced by the karyotyping of 1397 in-vitro unfertilized oocytes. Hum. Reprod. 17, 2134–2145 (2002).
Fragouli, E. et al. The cytogenetics of polar bodies: insights into female meiosis and the diagnosis of aneuploidy. Mol. Hum. Reprod. 17, 286–295 (2011).
Rabut, G. & Ellenberg, J. Automatic real-time three-dimensional cell tracking by fluorescence microscopy. J. Microsc. 216, 131–137 (2004).
We thank Dr J. Ellenberg for a macro for automated confocal microscopy, the CDB imaging and animal facilities for supports. This work was supported by a RIKEN Special Postdoctoral Fellowship to Y.S., grants from IVF Namba Clinic to S.H. and Y.N., grants from the Swedish Cancer Society, the Swedish Research Council and the Karolinska Institutet to C.H. and A.K., and grants from Nakajima Foundation, Uehara Memorial Foundation and RIKEN CDB to T.S.K.
The authors declare no competing financial interests.
Supplementary Figures 1-6 and Supplementary Tables 1. (PDF 1477 kb)
Live imaging of young BDF1 oocytes expressing 2mEGFP-CENP-C (green) and H2BmCherry (red). Images of 32 oocytes acquired in one experiment are shown. Time elapsed (hh:mm). Scale bar, 10 μm (MOV 2352 kb)
Images of an aged BDF1 oocyte expressing 2mEGFP-CENP-C (green) and H2BmCherry (blue) were reconstructed into 3D. All KTs were detected and tracked throughout MI. Colored spots indicate the KTs of a chromosome that underwent balanced predivision. Grid unit, 5 μm. Time after NEBD (hh:mm). See also Fig. 1a. (MOV 1098 kb)
Images of an aged BDF1 oocyte immunostained for KTs (ACA, green) and DNA (Hoechst33342, red) at metaphase II were reconstructed into 3D. This oocyte had 41 KTs. Grid unit, 2 μm. See also Supplementary Fig. 2a. (MOV 1521 kb)
Images of a BDF1 aged oocyte expressing 2mEGFP-CENP-C (green) and H2BmCherry (blue) were reconstructed into 3D. All homologous KTs were detected and tracked throughout MI. KT positions (spheres) and the connection of homologous KTs (lines). The S-chromosome is colored in green. The hyperstretched S-chromosome is colored in orange. The KT positions (spheres) and trajectories (lines) of the Schromosome exhibiting independent movements are colored in red and purple. Note that one bivalent underwent hyperstretching, and then independent KT movement, followed by predivision of sister chromatids. Grid unit, 5 μm. Time after NEBD (hh:mm). See also Fig. 2a. (MOV 1394 kb)
Images of a young Sycp3-/- oocyte expressing 2mEGFP-CENP-C (green) and H2BmCherry (blue) were reconstructed into 3D. All homologous KTs were detected and tracked throughout MI. KT positions (spheres) and the connection of homologous KTs (lines). The colored spots indicate the KTs of univalents. The KT positions (spheres) and trajectories (lines) of univalents are colored in red and purple. The set of univalents underwent unbalanced predivision. Grid unit, 5 μm. Time after NEBD (hh:mm). See also Supplementary Fig. 4a. (MOV 1789 kb)
Images of an aged BDF1 oocyte at late metaphase I were reconstructed into 3D. The, first round of the movie shows the immunofluorescence signals for KTs (ACA, green) and DNA (Hoechst 33342, red). The second round shows the positions of sister KTs (white spheres and lines). The third round shows the connections between homologous KTs (red lines). The sister KTs of univalents were indicated by magenta spheres and lines. See also Fig. 3b. (MOV 2603 kb)
Images of an oocyte from a 28-year-old patient were reconstructed into 3D. The first round of the movie shows the immunofluorescence signals for KTs (ACA, green) and DNA (Hoechst 33342, red). The second round shows the positions of sister KTs (white spheres and lines). The third round shows the connections between homologous KTs (red lines). See also Fig. 4a. (MOV 2566 kb)
Images of an oocyte from a 42-year-old patient were reconstructed into 3D. The first round of the movie shows the immunofluorescence signals for KTs (ACA, green) and DNA (Hoechst 33342, red). The second round shows the positions of sister KTs (white spheres and lines). The third round shows the connections between homologous KTs (red lines). The sister KTs of univalents were indicated by magenta spheres and lines. See also Fig. 4b. (MOV 2556 kb)
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Sakakibara, Y., Hashimoto, S., Nakaoka, Y. et al. Bivalent separation into univalents precedes age-related meiosis I errors in oocytes. Nat Commun 6, 7550 (2015). https://doi.org/10.1038/ncomms8550
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