Rec8-containing cohesin maintains bivalents without turnover during the growing phase of mouse oocytes
Open accessAbstract
During female meiosis, bivalent chromosomes are thought to be held together from birth until ovulation by sister chromatid cohesion mediated by cohesin complexes whose ring structure depends on kleisin subunits, either Rec8 or Scc1. Because cohesion is established at DNA replication in the embryo, its maintenance for such a long time may require cohesin turnover. To address whether Rec8- or Scc1-containing cohesin holds bivalents together and whether it turns over, we created mice whose kleisin subunits can be cleaved by TEV protease. We show by microinjection experiments and confocal live-cell imaging that Rec8 cleavage triggers chiasmata resolution during meiosis I and sister centromere disjunction during meiosis II, while Scc1 cleavage triggers sister chromatid disjunction in the first embryonic mitosis, demonstrating a dramatic transition from Rec8- to Scc1-containing cohesin at fertilization. Crucially, activation of an ectopic Rec8 transgene during the growing phase of Rec8 TEV / TEV oocytes does not prevent TEV-mediated bivalent destruction, implying little or no cohesin turnover for ≥2 wk during oocyte growth. We suggest that the inability of oocytes to regenerate cohesion may contribute to age-related meiosis I errors.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
For proteins with very slow turnover rates that surpass 48-72 h, RNAi approaches will not yield the desired knockdown of target transcripts.
“However, for those proteins that have very slow turnover rates that surpass this time frame [7], RNAi approaches will not yield the desired knockdown of target transcripts.”
From Advances in targeted degradation of endogenous proteins (2019) · cites this paper as [7]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 retracted
RETRACTED: Efficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain
Hayashi, S., Lewis, P. M., Pevny, L., & McMahon, A. P. (2002) · Gene Expression Patterns · doi:10.1016/s0925-4773(02)00292-7 · Cited by 113 · see citing works
RetractedTo err (meiotically) is human: the genesis of human aneuploidy
Hassold, T. J., & Hunt, P. A. (2001) · Nature Reviews Genetics · doi:10.1038/35066065 · Cited by 2,456 · see citing works
Cohesin: Its Roles and Mechanisms
Nasmyth, K., & Haering, C. H. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102108-134233 · Cited by 967 · see citing works
Self-citationCleavage of Cohesin by the CD Clan Protease Separin Triggers Anaphase in Yeast
Uhlmann, F., Wernic, D., Poupart, M., Koonin, E. V., & Nasmyth, K. (2000) · Cell · doi:10.1016/s0092-8674(00)00130-6 · Cited by 789 · see citing works
Self-citationPetronczki, M. P., Siomos, M. F., & Nasmyth, K. (2003) · Cell · doi:10.1016/s0092-8674(03)00083-7 · Cited by 704 · see citing works
Self-citationThe origin of human aneuploidy: where we have been, where we are going
Hassold, T. J., Hall, H., & Hunt, P. A. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm243 · Cited by 652 · see citing works
How Cells Get the Right Chromosomes
Nicklas, R. B. (1997) · Science · doi:10.1126/science.275.5300.632 · Cited by 610 · see citing works
The conserved kinetochore protein shugoshin protects centromeric cohesion during meiosis
Kitajima, T. S., Kawashima, S. A., & Watanabe, Y. (2004) · Nature · doi:10.1038/nature02312 · Cited by 579 · see citing works
Efficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain
Hayashi, S., Lewis, P. M., Pevny, L., & McMahon, A. P. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00099-6 · Cited by 492 · see citing works
The molecular foundations of the maternal to zygotic transition in the preimplantation embryo
Schultz, R. M. (2002) · Human Reproduction Update · doi:10.1093/humupd/8.4.323 · Cited by 481 · see citing works
Protein phosphatase 2A protects centromeric sister chromatid cohesion during meiosis I
Riedel, C. G., Katis, V. L., Katou, Y., Mori, S., Itoh, T., Helmhart, W., Gálová, M., Petronczki, M. P., Gregáň, J., Çetin, B., et al. (2006) · Nature · doi:10.1038/nature04664 · Cited by 455 · see citing works
Self-citationCohesion between sister chromatids must be established during DNA replication
Uhlmann, F., & Nasmyth, K. (1998) · Current Biology · doi:10.1016/s0960-9822(98)70463-4 · Cited by 454 · see citing works
Self-citationBuonomo, S. B. C., Clyne, R. K., Fuchs, J., Loidl, J., Uhlmann, F., & Nasmyth, K. (2000) · Cell · doi:10.1016/s0092-8674(00)00131-8 · Cited by 427 · see citing works
Self-citationHuman female meiosis: what makes a good egg go bad?
Hunt, P. A., & Hassold, T. J. (2008) · Trends in Genetics · doi:10.1016/j.tig.2007.11.010 · Cited by 370 · see citing works
Lewandoski, M. B., Wassarman, K. M., & Martin, G. R. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00059-5 · Cited by 354 · see citing works
Absence of Mouse REC8 Cohesin Promotes Synapsis of Sister Chromatids in Meiosis
Xu, H., Beasley, M. D., Warren, W., van der Horst, G. T. J., & McKay, M. J. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.03.018 · Cited by 352 · see citing works
DNA Double-Strand Breaks Trigger Genome-Wide Sister-Chromatid Cohesion Through Eco1 (Ctf7)
Ünal, E., Heidinger-Pauli, J. M., & Koshland, D. E. (2007) · Science · doi:10.1126/science.1140637 · Cited by 333 · see citing works
Structure and Stability of Cohesin's Smc1-Kleisin Interaction
Haering, C. H., Schoffnegger, D., Nishino, T., Helmhart, W., Nasmyth, K., & Löwe, J. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.08.030 · Cited by 322 · see citing works
Self-citationPostreplicative Formation of Cohesion Is Required for Repair and Induced by a Single DNA Break
Ström, L., Karlsson, C., Lindroos, H. B., Wedahl, S., Katou, Y., Shirahige, K., & Sjögren, C. (2007) · Science · doi:10.1126/science.1140649 · Cited by 320 · see citing works
Hodges, C. A., Revenkova, E., Jessberger, R., Hassold, T. J., & Hunt, P. A. (2005) · Nature Genetics · doi:10.1038/ng1672 · Cited by 318 · see citing works
Lan, Z., Xu, X., & Cooney, A. J. (2004) · Biology of Reproduction · doi:10.1095/biolreprod.104.031757 · Cited by 279 · see citing works
Cell-Type-Specific TEV Protease Cleavage Reveals Cohesin Functions in Drosophila Neurons
Pauli, A., Althoff, F., Oliveira, R. A., Heidmann, S. K., Schuldiner, O., Lehner, C. F., Dickson, B. J., & Nasmyth, K. (2008) · Developmental Cell · doi:10.1016/j.devcel.2007.12.009 · Cited by 276 · see citing works
Self-citationEijpe, M., Offenberg, H. H., Jessberger, R., Revenkova, E., & Heyting, C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212080 · Cited by 270 · see citing works
Unified mode of centromeric protection by shugoshin in mammalian oocytes and somatic cells
Lee, J., Kitajima, T. S., Tanno, Y., Yoshida, K., Morita, T., Miyano, T., Miyake, M., & Watanabe, Y. (2007) · Nature Cell Biology · doi:10.1038/ncb1667 · Cited by 263 · see citing works
Resolution of Chiasmata in Oocytes Requires Separase-Mediated Proteolysis
Kudo, N. R., Wassmann, K., Anger, M., et al. (2006) · Cell · doi:10.1016/j.cell.2006.05.033 · Cited by 242 · see citing works
Self-citationRegulation of APC/C Activity in Oocytes by a Bub1-Dependent Spindle Assembly Checkpoint
McGuinness, B. E., Anger, M., Kouznetsova, A., Gil-Bernabé, A. M., Helmhart, W., Kudo, N. R., Wünsche, A., Taylor, S. S., Höög, C., Novák, B., et al. (2009) · Current Biology · doi:10.1016/j.cub.2009.01.064 · Cited by 220 · see citing works
Self-citationGhosh, S., Feingold, E., & Dey, S. K. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32932 · Cited by 215 · see citing works
Activation of Specific Apoptotic Caspases with an Engineered Small-Molecule-Activated Protease
Gray, D. C., Mahrus, S., & Wells, J. A. (2010) · Cell · doi:10.1016/j.cell.2010.07.014 · Cited by 210 · see citing works
Metaphase I Arrest upon Activation of the Mad2-Dependent Spindle Checkpoint in Mouse Oocytes
Wassmann, K., Niault, T., & Maro, B. (2003) · Current Biology · doi:10.1016/j.cub.2003.08.052 · Cited by 209 · see citing works
SISTER-CHROMATID COHESION IN MITOSIS AND MEIOSIS
Miyazaki, W. Y., & Orr‐Weaver, T. L. (1994) · Annual Review of Genetics · doi:10.1146/annurev.ge.28.120194.001123 · Cited by 204 · see citing works
Rabitsch, K. P., Gregáň, J., Schleiffer, A., et al. (2004) · Current Biology · doi:10.1016/j.cub.2004.01.051 · Cited by 200 · see citing works
Chromosome Segregation in Mitosis and Meiosis
Murray, A. W., & Szostak, J. W. (1985) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.01.110185.001445 · Cited by 199 · see citing works
Katis, V. L., Lipp, J., Imre, R., et al. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.01.014 · Cited by 198 · see citing works
New Insights into Human Nondisjunction of Chromosome 21 in Oocytes
Oliver, T. R., Feingold, E., Yu, K., Cheung, V. G., Tinker, S. W., Yadav-Shah, M., Masse, N., & Sherman, S. L. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000033 · Cited by 197 · see citing works
Bannister, L., Reinholdt, L. G., Munroe, R. J., et al. (2004) · genesis · doi:10.1002/gene.20085 · Cited by 189 · see citing works
THE MOLECULAR AND CELLULAR BASIS OF PREIMPLANTATION MOUSE DEVELOPMENT
Johnson, M. H. (1981) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.1981.tb00356.x · Cited by 182 · see citing works
Lee, J., Iwai, T., Yokota, T., et al. (2003) · Journal of Cell Science · doi:10.1242/jcs.00495 · Cited by 180 · see citing works
Shugoshin-2 is essential for the completion of meiosis but not for mitotic cell division in micePreprint
Llano, E., Gómez, R., Gutiérrez‐Caballero, C., et al. (2008) · Genes & Development · doi:10.1101/gad.475308 · Cited by 177 · see citing works
Katis, V. L., Gálová, M., Rabitsch, K. P., Gregáň, J., & Nasmyth, K. (2004) · Current Biology · doi:10.1016/j.cub.2004.03.001 · Cited by 172 · see citing works
Self-citationShugoshin–PP2A counteracts casein-kinase-1-dependent cleavage of Rec8 by separase
Ishiguro, T., Tanaka, K., Sakuno, T., et al. (2010) · Nature Cell Biology · doi:10.1038/ncb2052 · Cited by 166 · see citing works
Cohesin cleavage and Cdk inhibition trigger formation of daughter nuclei
Oliveira, R. A., Hamilton, R. S., Pauli, A., Davis, I., & Nasmyth, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2018 · Cited by 165 · see citing works
Self-citationParra, M. T., Viera, A., Gómez, R., Page, J., Benavente, R., Santos, J. L., Rufas, J. S., & Suja, J. A. (2004) · Journal of Cell Science · doi:10.1242/jcs.00947 · Cited by 157 · see citing works
Automatic real‐time three‐dimensional cell tracking by fluorescence microscopy
Rabut, G. E. E., & Ellenberg, J. (2004) · Journal of Microscopy · doi:10.1111/j.0022-2720.2004.01404.x · Cited by 155 · see citing works
Rec8 cleavage by separase is required for meiotic nuclear divisions in fission yeast
Kitajima, T. S., Miyazaki, Y., Yamamoto, M., & Watanabe, Y. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg527 · Cited by 134 · see citing works
Defective cohesin is associated with age-dependent misaligned chromosomes in oocytes
Liu, L., & Keefe, D. L. (2008) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)60562-7 · Cited by 128 · see citing works
Cohesin component dynamics during meiotic prophase I in mammalian oocytes
Priéto, I., TEASE, C., Pezzi, N., Buesa, J. M., Ortega, S., Kremer, L., Martínez, A., Martínez‐A, C., Hultén, M. A., & Barbero, J. L. (2004) · Chromosome Research · doi:10.1023/b:chro.0000021945.83198.0e · Cited by 118 · see citing works
Role of cleavage by separase of the Rec8 kleisin subunit of cohesin during mammalian meiosis I
Kudo, N. R., Anger, M., Peters, A. H. F. M., Stemmann, O., Theussl, H., Helmhart, W., Kudo, H., Heyting, C., & Nasmyth, K. (2009) · Journal of Cell Science · doi:10.1242/jcs.035287 · Cited by 112 · see citing works
Self-citationA genome-wide, end-sequenced 129Sv BAC library resource for targeting vector construction
Adams, D. J., Quail, M. A., Cox, T., van der Weyden, L., Gorick, B. D., Su, Q., Chan, W.-I., Davies, R. M., Bonfield, J., Law, F., et al. (2005) · Genomics · doi:10.1016/j.ygeno.2005.08.003 · Cited by 112 · see citing works
Self-citationGómez, R., Valdeolmillos, A. M., Parra, M. T., et al. (2007) · EMBO Reports · doi:10.1038/sj.embor.7400877 · Cited by 107 · see citing works
The complete removal of cohesin from chromosome arms depends on separase
Nakajima, M., Kumada, K., Hatakeyama, K., et al. (2007) · Journal of Cell Science · doi:10.1242/jcs.011528 · Cited by 101 · see citing works
Vass, S., Cotterill, S., Valdeolmillos, A. M., Barbero, J. L., Lin, E., Warren, W. D., & Heck, M. M. S. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00047-2 · Cited by 101 · see citing works
Xu, H., Beasley, M. D., Verschoor, S., Inselman, A. L., Handel, M. A., & McKay, M. J. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400121 · Cited by 76 · see citing works
Clearing the way for mitosis: is cohesin a target?
Yanagida, M. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2712 · Cited by 66 · see citing works
Maguire, M. P. (1974) · Journal of Theoretical Biology · doi:10.1016/s0022-5193(74)80017-2 · Cited by 59 · see citing works
Control of Shugoshin Function during Fission-Yeast Meiosis
Vaur, S., Cubizolles, F., Plane, G., et al. (2005) · Current Biology · doi:10.1016/j.cub.2005.11.034 · Cited by 55 · see citing works
Chromosome cohesion – rings, knots, orcs and fellowship
Díaz-Martínez, L. A., Giménez-Abián, J. F., & Clarke, D. J. (2008) · Journal of Cell Science · doi:10.1242/jcs.029132 · Cited by 55 · see citing works
Sister chromatid cohesion: the cohesin cleavage model does not ring true
Guacci, V. (2007) · Genes to Cells · doi:10.1111/j.1365-2443.2007.01093.x · Cited by 51 · see citing works
Rabitsch, K. P. (2004) · Current Biology · doi:10.1016/s0960-9822(04)00063-6 · Cited by 45 · see citing works
Null and conditionalsemaphorin 3B alleles using a flexiblepuro?tk loxP/FRT vector
van der Weyden, L., Adams, D. J., Harris, L. W., Tannahill, D., Arends, M. J., & Bradley, A. (2005) · genesis · doi:10.1002/gene.20111 · Cited by 40 · see citing works
Self-citationLee, J., Yokota, T., & Yamashita, M. (2002) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.19.539 · Cited by 28 · see citing works
Cohesin Is Dispensable for Centromere Cohesion in Human Cells
Díaz-Martínez, L. A., Giménez-Abián, J. F., & Clarke, D. J. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000318 · Cited by 27 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Wutz, G., Várnai, C., Nagasaka, K., Cisneros, D. A., Stocsits, R. R., Tang, W., Schoenfelder, S., Jessberger, G., Muhar, M., Hossain, M. J., et al. (2017) · The EMBO Journal · doi:10.15252/embj.201798004 · Cited by 864 · see citing works
Identification of long-lived proteins reveals exceptional stability of essential cellular structures
Toyama, B. H., Savas, J. N., Park, S. K., Harris, M. S., Ingolia, N. T., Yates, J. R., & Hetzer, M. W. (2013) · Cell · doi:10.1016/j.cell.2013.07.037 · Cited by 572 · see citing works
A Method for the Acute and Rapid Degradation of Endogenous Proteins
Clift, D., McEwan, W. A., Labzin, L. I., Konieczny, V., Mogessie, B., James, L. C., & Schuh, M. (2017) · Cell · doi:10.1016/j.cell.2017.10.033 · Cited by 531 · see citing works
Cohesin is positioned in mammalian genomes by transcription, CTCF and Wapl
Busslinger, G. A., Stocsits, R. R., van der Lelij, P., Axelsson, E., Tedeschi, A., Galjart, N., & Peters, J.-M. (2017) · Nature · doi:10.1038/nature22063 · Cited by 468 · see citing works
Rapid movement and transcriptional re-localization of human cohesin on DNA
Davidson, I. F., Goetz, D., Zaczek, M. P., Molodtsov, M. I., Huis in 't Veld, P. J., Weissmann, F., Litos, G., Cisneros, D. A., Ocampo‐Hafalla, M., Ladurner, R., et al. (2016) · The EMBO Journal · doi:10.15252/embj.201695402 · Cited by 246 · see citing works
Advances in targeted degradation of endogenous proteins
Röth, S., Fulcher, L. J., & Sapkota, G. P. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03112-6 · Cited by 92 · see citing works
PP2A regulates kinetochore-microtubule attachment during meiosis I in oocyte
Tang, A., Shi, P., Song, A., Zou, D., Zhou, Y., Gu, P., Huang, Z., Wang, Q., Lin, Z., & Gao, X. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1175256 · Cited by 29 · see citing works
- Authors
- Tachibana-Konwalski, K., Godwin, J., van der Weyden, L., Champion, L., Kudo, N. R., Adams, D. J., & Nasmyth, K.
- Affiliations
- University of Oxford (GB)
- Imperial College London (GB)
- Wellcome Sanger Institute (GB)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2010-10-22
- Volume
- 24
- Issue
- 22
- Pages
- 2505-2516
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC2975927
- OpenAlex
- W2120439612
- Cited by
- 265
- References
- 61
- Citations by year
- 2026: 18 · 2025: 13 · 2024: 12 · 2023: 9 · 2022: 14 · 2021: 20 · 2020: 13 · 2019: 14 · 2018: 16 · 2017: 26 · 2016: 19 · 2015: 15 · 2014: 13 · 2013: 21 · 2012: 24
- Type
- posted content
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- Locations
- Genes & Development (publishedVersion, other-oa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- Cancer Research UK
- Kay Kendall Leukaemia Fund
- Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Reproductive Biology and Fertility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- REC8, Scc1, cohesin, sister chromatid cohesion, bivalent chromosomes, oocyte meiosis, oocyte growth, TEV protease cleavage, meiotic errors, mouse oocytes
- MeSH terms
- Cohesins, Animals, Cells, Cultured, Centromere, Chromosomal Proteins, Non-Histone, Chromosomes, Female, Nuclear Proteins, Oocytes, Endopeptidases, Phosphoproteins, Cell Cycle Proteins, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review