The DOI matches its Crossref record; 31 of the 32 references it cites were found in a registry or an index.
Restricted epigenetic inheritance of H3K9 methylation
Open accessAbstract
Inheritance of a covalent histone modification: Genomic DNA is the repository of all genetic information and is packaged into chromatin. Chromatin is also a repository of regulatory information in the form of covalent marks added to the histones that package the DNA. These marks can determine tissue- and organ-specific gene expression patterns, which must be transmitted to daughter cells to maintain their identity. Ragunathan et al. and Audergon et al. show that in fission yeast, a chromatin mark, like genetic information, can be inherited across many cell generations. The mark can be inherited independently of DNA sequence, DNA methylation, or RNA interference. Thus, histone marks constitute true epigenetic information. Science , this issue 10.1126/science.1258699 ; see also p. 132
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Indeed, inherited epigenetic patterns (254–256) and environmental factors (257, 258) other than childhood trauma (such as heavy metals (259), parenting style, and early trauma such as maternal separation (260)) may all impact the epigenetic pattern and hence childhood trauma-induced differential health outcomes.”
From Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma (2019) · cites this paper as [256]
Experimental — accuracy not yet measuredIn the citing paper
“By contrast, in the absence of RNAi-dependent amplification, H3K9me3 alone is insufficient to drive stable epigenetic memory, unless the histone demethylase Epe1 is mutated 47,102 .”
From Advances in epigenetics link genetics to the environment and disease (2019) · cites this paper as [102]
In the citing paper
“In yeast, TEI has been well-documented 101 and is known to involve RNAi-dependent heterochromatin deposition, leading to Clr4dependent H3K9me3 marking of silent heterochromatin 47,102 .”
From Advances in epigenetics link genetics to the environment and disease (2019) · cites this paper as [102]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Histone demethylation mediated by the nuclear amine oxidase homolog LSD1
Shi, Y., Lan, F., Matson, C., Mulligan, P., Whetstine, J. R., Cole, P. A., Casero, R. A., & Shi, Y. (2004) · Cell · doi:10.1016/j.cell.2004.12.012 · Cited by 4,051
Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain
Bannister, A. J., Zegerman, P., Partridge, J. F., Miska, E. A., Thomas, J. O., Allshire, R. C., & Kouzarides, T. (2001) · Nature · doi:10.1038/35065138 · Cited by 2,903
Self-citationMethylation of histone H3 lysine 9 creates a binding site for HP1 proteins
Lachner, M., O'Carroll, D., Rea, S., Mechtler, K., & Jenuwein, T. (2001) · Nature · doi:10.1038/35065132 · Cited by 2,868
Histone demethylation by a family of JmjC domain-containing proteins
Tsukada, Y.-I., Fang, J., Erdjument‐Bromage, H., Warren, M., Borchers, C. H., Tempst, P., & Zhang, Y. (2005) · Nature · doi:10.1038/nature04433 · Cited by 2,171
Role of Histone H3 Lysine 9 Methylation in Epigenetic Control of Heterochromatin Assembly
Nakayama, J.-I., Rice, J. C., Strahl, B. D., Allis, C. D., & Grewal, S. I. S. (2001) · Science · doi:10.1126/science.1060118 · Cited by 1,739
RNA interference in the nucleus: roles for small RNAs in transcription, epigenetics and beyond
Castel, S. E., & Martienssen, R. A. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3355 · Cited by 963
Dynamics and Memory of Heterochromatin in Living Cells
Hathaway, N. A., Bell, O., Hodges, C., Miller, E. L., Neel, D. S., & Crabtree, G. R. (2012) · Cell · doi:10.1016/j.cell.2012.03.052 · Cited by 446
Aagaard, L., Laible, G., Selenko, P., Schmid, M., Dorn, R., Schotta, G., Kuhfittig, S., Wolf, A., Lebersorger, A., Singh, P. B., et al. (1999) · The EMBO Journal · doi:10.1093/emboj/18.7.1923 · Cited by 441
Zhang, K., Mosch, K., Fischle, W., & Grewal, S. I. S. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1406 · Cited by 389
Cell cycle control of centromeric repeat transcription and heterochromatin assembly
Chen, E. S., Zhang, K., Nicolas, E., Cam, H. P., Zofall, M., & Grewal, S. I. S. (2008) · Nature · doi:10.1038/nature06561 · Cited by 356
Flagged first, then by citations
1 of the 32 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 101–200 of 254
Polymerase pausing induced by sequence-specific RNA-binding protein drives heterochromatin assemblyPreprint
Parsa, J., Boudoukha, S., Burke, J. E., Homer, C. M., & Madhani, H. D. (2018) · Genes & Development · doi:10.1101/gad.310136.117 · Cited by 36
Zofall, M., Sandhu, R., Holla, S., Wheeler, D. L., & Grewal, S. I. S. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00830-7 · Cited by 33
Greenstein, R. A., Jones, S. K., Spivey, E. C., Rybarski, J. R., Finkelstein, I. J., & Al‐Sady, B. (2018) · eLife · doi:10.7554/elife.32948 · Cited by 36
Shelterin and subtelomeric DNA sequences control nucleosome maintenance and genome stability
van Emden, T., Forn, M., Forné, I., Sarkadi, Z., Capella, M., Caballero, L. M., Fischer‐Burkart, S., Brönner, C., Simonetta, M., Toczyski, D. P., et al. (2018) · EMBO Reports · doi:10.15252/embr.201847181 · Cited by 35
Wiley, J. W., Zong, Y., Zheng, G., Zhu, S., & Hong, S. (2020) · Neurogastroenterology & Motility · doi:10.1111/nmo.13941 · Cited by 35
The molecular basis of cell memory in mammals: The epigenetic cycle
Espinosa-Martínez, M., Alcázar‐Fabra, M., & Landeira, D. (2024) · Science Advances · doi:10.1126/sciadv.adl3188 · Cited by 35
Sahu, R. K., Dhakshnamoorthy, J., Jain, S., Folco, H. D., Wheeler, D. L., & Grewal, S. I. S. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.07.006 · Cited by 36
Raiymbek, G., An, S., Khurana, N., Gopinath, S., Larkin, A., Biswas, S., Trievel, R. C., Cho, U., & Ragunathan, K. (2020) · eLife · doi:10.7554/elife.53155 · Cited by 33
Epigenomic insights into common human disease pathology
Bell, C. G. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05206-2 · Cited by 36
Cis-acting determinants of paramutation
Hövel, I., Pearson, N. A., & Stam, M. E. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.08.012 · Cited by 31
Establishment of expression-state boundaries by Rif1 and Taz1 in fission yeast
Toteva, T., Mason, B., Kanoh, Y., Brøgger, P., Green, D., Verhein-Hansen, J., Masai, H., & Thon, G. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1614837114 · Cited by 31
Heurteau, A., Perrois, C., Depierre, D., Fosseprez, O., Humbert, J., Schaak, S., & Cuvier, O. (2020) · Genome biology · doi:10.1186/s13059-020-02106-z · Cited by 32
Wang, X., Paulo, J. A., Li, X., Zhou, H., Yu, J., Gygi, S. P., & Moazed, D. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.07.017 · Cited by 26
The Inherent Asymmetry of DNA Replication
Snedeker, J. C., Wooten, M., & Chen, X. (2017) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100616-060447 · Cited by 34
Sanchez, N. A., Kallweit, L. M., Trnka, M. J., Clemmer, C. L., & Al‐Sady, B. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101276 · Cited by 25
Transgenerational epigenetic inheritance: a critical perspective
Bird, A. P. (2024) · Frontiers in Epigenetics and Epigenomics · doi:10.3389/freae.2024.1434253 · Cited by 32
Establishment of heterochromatin in domain-size-dependent bursts
Nickels, J. F., Edwards, A., Charlton, S. J., Mortensen, A. M., Hougaard, S. C. L., Trusina, A., Sneppen, K., & Thon, G. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2022887118 · Cited by 27
Abdulla, A. Z., Vaillant, C., & Jost, D. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac702 · Cited by 26
Sorida, M., Hirauchi, T., Ishizaki, H., Kaito, W., Shimada, A., Mori, C., Chikashige, Y., Hiraoka, Y., Suzuki, Y., Ohkawa, Y., et al. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008129 · Cited by 27
Zhang, J., Donahue, G., Gilbert, M. B., Lapidot, T., Nicetto, D., & Zaret, K. S. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01547-z · Cited by 33
Erdel, F. (2017) · BioEssays · doi:10.1002/bies.201700053 · Cited by 28
Symmetry from Asymmetry or Asymmetry from Symmetry?Preprint
Kahney, E. W., Ranjan, R., Gleason, R. J., & Chen, X. (2017) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2017.82.034272 · Cited by 23
Disruption of promoter memory by synthesis of a long noncoding RNA
Yu, Y., Yarrington, R. M., Chuong, E. B., Elde, N. C., & Stillman, D. J. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601793113 · Cited by 26
Georgescu, P. R., Capella, M., Fischer‐Burkart, S., & Braun, S. J. (2020) · Microbial Cell · doi:10.15698/mic2020.03.711 · Cited by 24
The INO80 Complex Regulates Epigenetic Inheritance of Heterochromatin
Shan, C., Bao, K., Diedrich, J. K., Chen, X., Lü, C., Yates, J. R., & Jia, S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108561 · Cited by 24
Coordination of histone chaperones for parental histone segregation and epigenetic inheritancePreprint
Fang, Y., Hua, X., Shan, C.-M., Toda, T., Qiao, F., Zhang, Z., & Jia, S. (2024) · Genes & Development · doi:10.1101/gad.351278.123 · Cited by 21
A unifying model of epigenetic regulation
Keung, A. J., & Khalil, A. S. (2016) · Science · doi:10.1126/science.aaf1647 · Cited by 21
Requirements for establishment and epigenetic stability of mammalian heterochromatin
Tatarakis, A., Saini, H., Yu, J., Feng, W., Pinzón-Arteaga, C. A., & Moazed, D. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.08.025 · Cited by 24
H3K9 demethylases IBM1 and JMJ27 are required for male meiosis in Arabidopsis thaliana
Cheng, J., Xu, L., Bergér, V., Bruckmann, A., Yang, C., Schubert, V., Grasser, K. D., Schnittger, A., Zheng, B., & Jiang, H. L. (2022) · New Phytologist · doi:10.1111/nph.18286 · Cited by 21
Nathanailidou, P., Dhakshnamoorthy, J., Xiao, H., Zofall, M., Holla, S., O’Neill, M. J., Andrésson, Þ., Wheeler, D. L., & Grewal, S. I. S. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2315596121 · Cited by 21
The evolutionary consequences of interactions between the epigenome, the genome and the environment
Baduel, P., Sammarco, I., Barrett, R. D. H., Coronado‐Zamora, M., Crespel, A., Rodríguez, B. D., Fox, J. A., Galanti, D., González, J., Jueterbock, A., et al. (2024) · Evolutionary Applications · doi:10.1111/eva.13730 · Cited by 23
Martins, N. M. C., Cisneros-Soberanis, F., Pesenti, E., Kochanova, N. Y., Shang, W.-H., Hori, T., Nagase, T., Kimurâ, H., Larionov, V., Masumoto, H., et al. (2020) · Journal of Cell Science · doi:10.1242/jcs.242610 · Cited by 21
Yaseen, I., White, S. A., Torres-Garcia, S., Spanos, C., Lafos, M., Gaberdiel, E., Yeboah, R., El Karoui, M., Rappsilber, J., Pidoux, A. L., et al. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00801-y · Cited by 20
Self-citationDistinct silencer states generate epigenetic states of heterochromatin
Saxton, D. S., & Rine, J. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.08.002 · Cited by 21
Environmental epigenetics: new horizons in redefining biological and health outcomes
Faraji, J., & Metz, G. A. S. (2026) · Environment International · doi:10.1016/j.envint.2026.110072 · Cited by 22
Epigenetic Mechanisms of Tree Responses to Climatic Changes
Kurpisz, B., & Pawłowski, T. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113412 · Cited by 21
RNA quality control factors nucleate Clr4/SUV39H and trigger constitutive heterochromatin assembly
Khanduja, J. S., Joh, R. I., Perez, M. M., Paulo, J. A., Palmieri, C. M., Zhang, J., Gulka, A. O. D., Haas, W., Gygi, S. P., & Motamedi, M. (2024) · Cell · doi:10.1016/j.cell.2024.04.042 · Cited by 20
Recruitment and reinforcement: maintaining epigenetic silencing
Wang, C., Zhu, B., & Xiong, J. (2018) · Science China Life Sciences · doi:10.1007/s11427-018-9276-7 · Cited by 19
Padmasekar, M., Savai, R., Seeger, W., & Pullamsetti, S. S. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18168280 · Cited by 18
RNAi epimutations conferring antifungal drug resistance are inheritable
Arques, C. P., Navarro-Mendoza, M. I., Xu, Z., Walther, G., & Heitman, J. (2025) · Nature Communications · doi:10.1038/s41467-025-62572-6 · Cited by 19
Retrieving Chromatin Patterns from Deep Sequencing Data Using Correlation Functions
Molitor, J., Mallm, J., Rippe, K., & Erdel, F. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2017.01.001 · Cited by 17
Seman, M., Levashkevich, A., Larkin, A., Huang, F., & Ragunathan, K. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113428 · Cited by 16
Brickner, J. H. (2023) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15033 · Cited by 17
A Heterochromatin Domain Forms Gradually at a New Telomere and Is Dynamic at Stable Telomeres
Wang, J., Eisenstatt, J. R., Audry, J., Cornelius, K., Shaughnessy, M. P., Berkner, K. L., & Runge, K. W. (2018) · Molecular and Cellular Biology · doi:10.1128/mcb.00393-17 · Cited by 19
Nuclear Envelope Proteins Modulating the Heterochromatin Formation and Functions in Fission Yeast
Hirano, Y., Asakawa, H., Sakuno, T., Haraguchi, T., & Hiraoka, Y. (2020) · Cells · doi:10.3390/cells9081908 · Cited by 16
Molecular and cellular bases of trained immunity
Sun, S. J., Aguirre‐Gamboa, R., & Barreiro, L. B. (2026) · Immunity · doi:10.1016/j.immuni.2026.03.001 · Cited by 18
Liu, Z., Liu, J., Liu, F., & Zhong, X. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad306 · Cited by 15
Chromatin‐associated noncoding RNAs in development and inheritance
Acharya, S., Hartmann, M., & Erhardt, S. (2017) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1435 · Cited by 15
Paraquat Reduces the Female Fertility by Impairing the Oocyte Maturation in Mice
Sun, Y., Wang, X., Yang, L., Ge, Z., Zhao, Y. M., Luo, S., Shen, W., Sun, Q., & Yin, S. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.631104 · Cited by 15
Evolution of epigenetic chromatin states
Yung, P. Y. K., & Elsässer, S. J. (2017) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2017.10.001 · Cited by 15
Ancona, M., Michieletto, D., & Marenduzzo, D. (2020) · Physical review. E · doi:10.1103/physreve.101.042408 · Cited by 13
Wang, L., Liu, J., Li, X., Lyu, X., Liu, Z., Zhao, H., Jiao, X., Zhang, W., Xie, J., & Liu, W. (2022) · Microbial Biotechnology · doi:10.1111/1751-7915.14103 · Cited by 14
Histone H3K9 demethylase JMJD1A is a co-activator of erythropoietin expression under hypoxia
Tian, Z., Lv, Y., Shen, Y., Guo, X., & Duan, X. (2019) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2019.01.022 · Cited by 13
Recycling of parental histones preserves the epigenetic landscape during embryonic development
Mühlen, D., Li, X., Dovgusha, O., Jäckle, H., & Günesdogan, U. (2023) · Science Advances · doi:10.1126/sciadv.add6440 · Cited by 13
Beyond Tethering and the LEM domain: MSCellaneous functions of the inner nuclear membrane Lem2
Braun, S. J., & Barrales, R. R. (2016) · Nucleus · doi:10.1080/19491034.2016.1252892 · Cited by 13
Chang, R. C.-A., Thomas, K. N., Mehta, N. A., Veazey, K. J., Parnell, S. E., & Golding, M. C. (2021) · Epigenetics & Chromatin · doi:10.1186/s13072-021-00403-w · Cited by 13
Al‐Sady, B., Greenstein, R., El‐Samad, H., Braun, S. J., & Madhani, H. D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159292 · Cited by 13
High-throughput assessment of context-dependent effects of chromatin proteins
Brueckner, L., van Arensbergen, J., Akhtar, W., Pagie, L., & van Steensel, B. (2016) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0096-y · Cited by 13
Mkt1 is required for RNAi-mediated silencing and establishment of heterochromatin in fission yeast
Taglini, F., Chapman, E., van Nues, R. W., Théron, E., & Bayne, E. H. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1157 · Cited by 13
Epigenome Editing in the Brain
Bashtrykov, P., & Jeltsch, A. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-53889-1_21 · Cited by 12
Establishment of centromere identity is dependent on nuclear spatial organization
Wu, W., McHugh, T., Kelly, D. A., Pidoux, A. L., & Allshire, R. C. (2022) · Current Biology · doi:10.1016/j.cub.2022.06.048 · Cited by 11
Self-citationMarayati, B. F., Tucker, J. F., de la Cerda, D. A., Hou, T.-C. J., Chen, R., Sugiyama, T., Pease, J. B., & Zhang, K. (2020) · Cells · doi:10.3390/cells9040955 · Cited by 11
Raboni, S., Montalbano, S., Stransky, S., Garcia, B. A., Buschini, A., Bettati, S., Sidoli, S., & Mozzarelli, A. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.735303 · Cited by 19
Asanuma, T., Inagaki, S., Kakutani, T., Aburatani, H., & Murakami, Y. (2022) · Genes & Development · doi:10.1101/gad.350129.122 · Cited by 10
Mapping the dynamics of epigenetic adaptation in S. pombe during heterochromatin misregulation
Larkin, A., Kunze, C., Seman, M., Levashkevich, A., Curran, J., Morris-Evans, D., Lemieux, S., Khalil, A. S., & Ragunathan, K. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.07.006 · Cited by 10
Kollenstart, L., Biran, A., Alcaraz, N., Reverón-Gómez, N., Solis‐Mezarino, V., Völker-Albert, M. C., Jenkinson, F., Flury, V., & Groth, A. (2025) · Science Advances · doi:10.1126/sciadv.adr1453 · Cited by 10
Clr4 specificity and catalytic activity beyond H3K9 methylation
Kušević, D., Kudithipudi, S., Iglesias, N., Moazed, D., & Jeltsch, A. (2017) · Biochimie · doi:10.1016/j.biochi.2017.01.013 · Cited by 10
Adaptive Evolution and Epigenetics
Kronholm, I. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805388-1.00028-6 · Cited by 11
The cAMP signaling pathway regulates Epe1 protein levels and heterochromatin assembly
Bao, K., Shan, C., Chen, X., Raiymbek, G., Monroe, J. G., Fang, Y., Toda, T., Koutmou, K. S., Ragunathan, K., Lü, C., et al. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010049 · Cited by 9
Tissue homogeneity requires inhibition of unequal gene silencing during development
Lê, H. M. N., Looney, M. M., Strauss, B., Bloodgood, M., & Jose, A. M. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201601050 · Cited by 9
Leaving histone unturned for epigenetic inheritance
Shan, C., Fang, Y., & Jia, S. (2021) · FEBS Journal · doi:10.1111/febs.16260 · Cited by 9
Histone variant H2A.Z plays multiple roles in the maintenance of heterochromatin integrity
Tsukii, K., Takahata, S., & Murakami, Y. (2021) · Genes to Cells · doi:10.1111/gtc.12911 · Cited by 9
Stress controls heterochromatin inheritance via histone H3 ubiquitylation
Bhatt, B., Wei, Y., Pradhan, A. K., Dhakshnamoorthy, J., Zofall, M., Xiao, H., Vijayakumari, D., Jain, S., Folco, H. D., Qi, H., et al. (2026) · Nature · doi:10.1038/s41586-025-09899-8 · Cited by 8
Transgenerational epigenetic control of constitutive heterochromatin, transposons, and centromeres
Fukagawa, T., & Kakutani, T. (2023) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2023.102021 · Cited by 8
Bártová, E., Večeřa, J., Krejčí, J., Legartová, S., Pachernı́k, J., & Kozubek, S. (2016) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1402-7 · Cited by 8
Passing epigenetic silence to the next generation
De, S., & Kassis, J. A. (2017) · Science · doi:10.1126/science.aan1493 · Cited by 8
Deposition Bias of Chromatin Proteins Inverts under DNA Replication Stress Conditions
Zwinderman, M. R. H., Lobo, T. J., van der Wouden, P. E., Spierings, D. C. J., van Vugt, M. A. T. M., Lansdorp, P. M., Guryev, V., & Dekker, F. J. (2021) · ACS Chemical Biology · doi:10.1021/acschembio.1c00321 · Cited by 7
Antimicrobial resistance in the wild: Insights from epigenetics
de la Peña, M. V., & Kronholm, I. (2024) · Evolutionary Applications · doi:10.1111/eva.13707 · Cited by 7
Analysis of Heterochromatin in Schizosaccharomyces pombePreprint
Cam, H. P., & Whitehall, S. K. (2016) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top079889 · Cited by 7
Replication-coupled inheritance of chromatin states
Song, A., Wang, Y., Liu, C., Yu, J., Zhang, Z., Lan, L., Lin, H., Zhao, J., & Li, G. (2024) · Cell Insight · doi:10.1016/j.cellin.2024.100195 · Cited by 6
Minimal requirements for the epigenetic inheritance of engineered silent chromatin domains
Yuan, A. H., & Moazed, D. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2318455121 · Cited by 6
time-ChIP: A Method to Determine Long-Term Locus-Specific Nucleosome Inheritance
Siwek, W., Rodríguez, M. G., Sobral, D., Junior, I. R. C., & Jansen, L. E. T. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8663-7_7 · Cited by 6
Application of Recombination -Induced Tag Exchange (RITE) to study histone dynamics in human cells
Molenaar, T. M., Pagès-Gallego, M., Meyn, V., & van Leeuwen, F. (2020) · Epigenetics · doi:10.1080/15592294.2020.1741777 · Cited by 7
Unprogrammed epigenetic variation mediated by stochastic formation of ectopic heterochromatin
Sorida, M., & Murakami, Y. (2019) · Current Genetics · doi:10.1007/s00294-019-01031-4 · Cited by 5
Adaptive evolution and epigenetics
Kronholm, I. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91909-8.00014-1 · Cited by 5
Qin, L., Gong, X., Nong, J., Tang, X., Cui, K., Zhao, Y., & Xia, S. (2024) · Journal of Fungi · doi:10.3390/jof10040271 · Cited by 5
Mrc1Claspin is essential for heterochromatin maintenance in Schizosaccharomyces pombe
Kawakami, K., Ueno, Y., Hayama, N., & Tanaka, K. (2024) · Genes to Cells · doi:10.1111/gtc.13175 · Cited by 5
Condensin IDC, DPY-21, and CEC-4 maintain X chromosome repression in C. elegans
Trombley, J., Rakozy, A. I., McClear, C. A., Jash, E., & Csankovszki, G. (2025) · PLoS Genetics · doi:10.1371/journal.pgen.1011247 · Cited by 4
Heterochromatin epimutations impose mitochondrial dysfunction to confer antifungal resistance
Fellas, A., Pidoux, A. L., Tong, P., Hewes, H. H., Wallace, E. C., & Allshire, R. C. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00649-0 · Cited by 4
Self-citationThe influence of high-order chromatin state in the regulation of stem cell fate
Chen, X., Lin, H., & Li, G. (2022) · Biochemical Society Transactions · doi:10.1042/bst20220763 · Cited by 4
Lin, H., Pan, Y., & Cai, S. (2023) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szad019 · Cited by 5
Challal, D., Menant, A., Goksal, C., Leroy, E., Al‐Sady, B., & Rougemaille, M. (2023) · Genetics · doi:10.1093/genetics/iyad108 · Cited by 4
Ames, A., Seman, M., Larkin, A., Raiymbek, G., Chen, Z., Levashkevich, A., Kim, B., Biteen, J. S., & Ragunathan, K. (2024) · Nature Communications · doi:10.1038/s41467-024-50538-z · Cited by 5
Muhammad, A., Sarkadi, Z., Mazumder, A., Saada, A. A., van Emden, T., Capella, M., Fekete, G., Sreechakram, V. N. S., Al‐Sady, B., Lambert, S., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1024 · Cited by 4
Insights in human epigenomic dynamics through comparative primate analysis
Bell, C. G. (2016) · Genomics · doi:10.1016/j.ygeno.2016.09.003 · Cited by 4
Advances in Approaches to Study Chromatin-Mediated Epigenetic Memory
Yao, Y., Wen, Q., Zhang, T., Yu, C., Chan, K. M., & Gan, H. (2021) · ACS Synthetic Biology · doi:10.1021/acssynbio.1c00394 · Cited by 4
Ramsey, J. S., Zhong, X., Saha, S., Chavez, J. D., Johnson, R. S., Mahoney, J. E., Keller, A., Moulton, K., Mueller, L. A., Hall, D. G., et al. (2022) · ACS Agricultural Science & Technology · doi:10.1021/acsagscitech.1c00264 · Cited by 4
Investigating Mitotic Inheritance of Histone Modifications Using Tethering Strategies
Larkin, A., Ames, A., Seman, M., & Ragunathan, K. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2481-4_18 · Cited by 4
Croft, J. C., Colunga, A., Solh, L., Dillon, M. K., & Lee, T. W.-S. (2022) · PubMed Central · doi:10.17912/micropub.biology.000719 · Cited by 4
Silencing and anti-silencing mechanisms that shape the epigenome in plants
Inagaki, S. (2021) · Genes & Genetic Systems · doi:10.1266/ggs.21-00041 · Cited by 4
Metadata
- Authors
- Audergon, P. N. C. B., Catania, S., Kagansky, A., Tong, P., Shukla, M., Pidoux, A. L., & Allshire, R. C.
- Affiliations
- Wellcome Centre for Cell Biology (GB)
- Corresponding author
- Allshire, Robin C.
- ORCID
- Venue
- Science
- Published
- 2015-04-03
- Volume
- 348
- Issue
- 6230
- Pages
- 132-135
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4397586
- OpenAlex
- W2105077884
- Cited by
- 254
- References
- 32
- Citations by year
- 2026: 14 · 2025: 10 · 2024: 29 · 2023: 20 · 2022: 21 · 2021: 23 · 2020: 26 · 2019: 22 · 2018: 15 · 2017: 35 · 2016: 26 · 2015: 13
- FWCI
- 12.88
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- ERA (submittedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Funders
- Wellcome Trust (93852)
- Wellcome Trust Principal Research Fellowship (95021)
- EC-NOE-EpiGeneSys (HEALTH-F4-2010-257082)
- Wellcome Trust Centre for Cell Biology (92076)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- H3K9 methylation, epigenetic inheritance, heterochromatin, Clr4, histone demethylase, histone methyltransferase, transgenerational inheritance, meiosis, mitotic inheritance, Schizosaccharomyces pombe
- MeSH terms
- Heterochromatin, Histones, Lysine, Methylation, Methyltransferases, Mutation, Nuclear Proteins, Histone-Lysine N-Methyltransferase, Protein Processing, Post-Translational, Schizosaccharomyces, Cell Cycle Proteins, Schizosaccharomyces pombe Proteins, Epigenesis, Genetic
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