The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
AURKB-driven dissolution of CIZ1–RNA assemblies from the inactive X chromosome in mitosis
Open accessPublished version of a preprint
Abstract
Cip1-interacting zinc-finger protein 1 (CIZ1) interacts with Xist lncRNA to form large RNA–protein assemblies at the inactive X-chromosome (Xi) in female mammalian nuclei, plus smaller assemblies in both sexes. CIZ1 assemblies influence underlying chromatin, and their disruption alters the expression of autosomal and X-linked gene clusters. Here, we explore the regulated dissolution of CIZ1–Xi assemblies during mitosis and show that, like Xist, CIZ1 is released in prometaphase under the regulation of Aurora Kinase B (AURKB). The part of human/mouse CIZ1 comprising 179/181 C-terminal amino acids encodes a matrin-3 domain that facilitates dimerization to form a compact folded core with disordered C-terminal extensions. Mass spectrometry revealed 56 high-confidence interacting partners of the C-terminal fragment, predominantly chromatin, nuclear matrix, and RNA-binding proteins. Phosphomimetic mutation of three conserved AURKB sites in the C-terminal extensions released CIZ1 from its nuclear anchor points, but did not affect its interaction with chromatin or nuclear matrix proteins. In contrast, the same mutations, or deletion of the C-terminal extensions, abolished interaction with RNAs, including Xist. Together, the data suggest CIZ1 is a regulatable component of the protein–RNA assemblies that preserve epigenetic stability across the nucleus, and that AURKB drives their dissolution in mitosis via dissociation of CIZ1 from RNA.
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.
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
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Flagged first, then by citations
Research works printed but not linked: 63
- Berezney, 1974, Identification of a nuclear protein matrix, Biochem Biophys Res Commun, 60, 1410, 10.1016/0006-291X(74)90355-6 · DOI
- Nickerson, 2022, The ribonucleoprotein network of the nucleus: a historical perspective, Curr Opin Genet Dev, 75, 101940, 10.1016/j.gde.2022.101940 · DOI
- Cerase, 2019, Phase separation drives X-chromosome inactivation: a hypothesis, Nat Struct Mol Biol, 26, 331, 10.1038/s41594-019-0223-0 · DOI
- Ainscough, 2007, C-terminal domains deliver the DNA replication factor Ciz1 to the nuclear matrix, J Cell Sci, 120, 115, 10.1242/jcs.03327 · DOI
- Ridings-Figueroa, 2017, The nuclear matrix protein CIZ1 facilitates localization of xist RNA to the inactive X-chromosome territory, Genes Dev, 31, 876, 10.1101/gad.295907.117 · DOI
- Sunwoo, 2017, Repeat E anchors xist RNA to the inactive X chromosomal compartment through CDKN1A-interacting protein (CIZ1), Proc Natl Acad Sci USA, 114, 10654, 10.1073/pnas.1711206114 · DOI
- Markaki, 2021, Xist nucleates local protein gradients to propagate silencing across the X chromosome, Cell, 184, 6174, 10.1016/j.cell.2021.10.022 · DOI
- Stewart, 2019, Maintenance of epigenetic landscape requires CIZ1 and is corrupted in differentiated fibroblasts in long-term culture, Nat Commun, 10, 460, 10.1038/s41467-018-08072-2 · DOI
- Sofi, 2022, Prion-like domains drive CIZ1 assembly formation at the inactive X chromosome, J Cell Biol, 221, e202103185, 10.1083/jcb.202103185 · DOI
- Turvey, 2025, Epigenetic deprogramming by disruption of CIZ1–RNA nuclear assemblies in early-stage breast cancers, J Cell Biol, 224, e202409123, 10.1083/jcb.202409123 · DOI
- Mortlock, 2007, Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of aurora B kinase, J Med Chem, 50, 2213, 10.1021/jm061335f · DOI
- Coverley, 2005, Ciz1 promotes mammalian DNA replication, J Cell Sci, 118, 101, 10.1242/jcs.01599 · DOI
- Coverley, 2002, Distinct roles for cyclins E and A during DNA replication complex assembly and activation, Nat Cell Biol, 4, 523, 10.1038/ncb813 · DOI
- Wutz, 2000, A shift from reversible to irreversible X inactivation is triggered during ES cell differentiation, Mol Cell, 5, 695, 10.1016/S1097-2765(00)80248-8 · DOI
- Mohammed, 2016, Rapid immunoprecipitation mass spectrometry of endogenous proteins (RIME) for analysis of chromatin complexes, Nat Protoc, 11, 316, 10.1038/nprot.2016.020 · DOI
- Yu, 2020, Fast quantitative analysis of timsTOF PASEF data with MSFragger and IonQuant, Mol Cell Proteomics, 19, 1575, 10.1074/mcp.TIR120.002048 · DOI
- Ritchie, 2015, limma powers differential expression analyses for RNA-sequencing and microarray studies, Nucleic Acids Res, 43, e47, 10.1093/nar/gkv007 · DOI · Paper page
- Hsiao, 2024, Analysis and visualization of quantitative proteomics data using FragPipe-analyst, J Proteome Res, 23, 4303, 10.1021/acs.jproteome.4c00294 · DOI
- Schindelin, 2012, Fiji: an open-source platform for biological-image analysis, Nat Methods, 9, 676, 10.1038/nmeth.2019 · DOI · Paper page
- Szklarczyk, 2023, The STRING database in 2023: protein–protein association networks and functional enrichment analyses for any sequenced genome of interest, Nucleic Acids Res, 51, D638, 10.1093/nar/gkac1000 · DOI · Paper page
- Wang, 2020, GPS 5.0: an update on the prediction of kinase-specific phosphorylation sites in proteins, Genomics Proteomics Bioinformatics, 18, 72, 10.1016/j.gpb.2020.01.001 · DOI
- Shannon, 2003, Cytoscape: a software environment for integrated models of biomolecular interaction networks, Genome Res, 13, 2498, 10.1101/gr.1239303 · DOI · Paper page
- Waterhouse, 2009, Jalview Version 2—a multiple sequence alignment editor and analysis workbench, Bioinformatics, 25, 1189, 10.1093/bioinformatics/btp033 · DOI
- da Veiga Leprevost, 2020, Philosopher: a versatile toolkit for shotgun proteomics data analysis, Nat Methods, 17, 869, 10.1038/s41592-020-0912-y · DOI
- Yu, 2021, IonQuant enables accurate and sensitive label-free quantification with FDR-controlled match-between-runs, Mol Cell Proteomics, 20, 100077, 10.1016/j.mcpro.2021.100077 · DOI
- Kettenbach, 2011, Quantitative phosphoproteomics identifies substrates and functional modules of Aurora and Polo-like kinase activities in mitotic cells, Sci Signal, 4, rs5, 10.1126/scisignal.2001497 · DOI
- Dixon-McDougall, 2022, Multiple distinct domains of human XIST are required to coordinate gene silencing and subsequent heterochromatin formation, Epigenetics Chromatin, 15, 6, 10.1186/s13072-022-00438-7 · DOI
- Valledor, 2023, Early chromosome condensation by XIST builds A-repeat RNA density that facilitates gene silencing, Cell Rep, 42, 112686, 10.1016/j.celrep.2023.112686 · DOI
- Duthie, 1999, Xist RNA exhibits a banded localization on the inactive X chromosome and is excluded from autosomal material in cis, Hum Mol Genet, 8, 195, 10.1093/hmg/8.2.195 · DOI
- Hall, 2009, AURKB-mediated effects on chromatin regulate binding versus release of XIST RNA to the inactive chromosome, J Cell Biol, 186, 491, 10.1083/jcb.200811143 · DOI
- Cohen, 1990, Okadaic acid: a new probe for the study of cellular regulation, Trends Biochem Sci, 15, 98, 10.1016/0968-0004(90)90192-E · DOI
- Hori, 1991, A novel protein phosphatase inhibitor, tautomycin. Effect on smooth muscle, FEBS Lett, 285, 145, 10.1016/0014-5793(91)80745-O · DOI
- Sharp, 2020, Cell division requires RNA eviction from condensing chromosomes, J Cell Biol, 219, e201910148, 10.1083/jcb.201910148 · DOI
- Nozawa, 2017, SAF-A regulates interphase chromosome structure through oligomerization with chromatin-associated RNAs, Cell, 169, 1214, 10.1016/j.cell.2017.05.029 · DOI
- Helbig, 2003, Scaffold attachment factor A (SAF-A) is concentrated in inactive X chromosome territories through its RGG domain, Chromosoma, 112, 173, 10.1007/s00412-003-0258-0 · DOI
- Hasegawa, 2010, The matrix protein hnRNP U is required for chromosomal localization of xist RNA, Dev Cell, 19, 469, 10.1016/j.devcel.2010.08.006 · DOI
- Chu, 2015, Systematic discovery of Xist RNA binding proteins, Cell, 161, 404, 10.1016/j.cell.2015.03.025 · DOI
- Minajigi, 2015, Chromosomes. A comprehensive xist interactome reveals cohesin repulsion and an RNA-directed chromosome conformation, Science, 349, 10.1126/science.aab2276, 10.1126/science.aab2276 · DOI
- McHugh, 2015, The xist lncRNA interacts directly with SHARP to silence transcription through HDAC3, Nature, 521, 232, 10.1038/nature14443 · DOI
- Moindrot, 2016, RNA binding proteins implicated in Xist-mediated chromosome silencing, Semin Cell Dev Biol, 56, 58, 10.1016/j.semcdb.2016.01.029 · DOI
- Monfort, 2015, Identification of spen as a crucial factor for xist function through forward genetic screening in haploid embryonic stem cells, Cell Rep, 12, 554, 10.1016/j.celrep.2015.06.067 · DOI
- Thacker, 2020, Identification of DHX9 as a cell cycle regulated nucleolar recruitment factor for CIZ1, Sci Rep, 10, 18103, 10.1038/s41598-020-75160-z · DOI
- Ludérus, 1994, Binding of matrix attachment regions to lamin polymers involves single-stranded regions and the minor groove, Mol Cell Biol, 14, 6297
- Norman, 2016, The increasing diversity of functions attributed to the SAFB family of RNA-/DNA-binding proteins, Biochem J, 473, 4271, 10.1042/BCJ20160649 · DOI
- Townson, 2003, SAFB2, a new scaffold attachment factor homolog and estrogen receptor corepressor*, J Biol Chem, 278, 20059, 10.1074/jbc.M212988200 · DOI
- Huttlin, 2021, Dual proteome-scale networks reveal cell-specific remodeling of the human interactome, Cell, 184, 3022, 10.1016/j.cell.2021.04.011 · DOI · Paper page
- Mirdita, 2022, ColabFold: making protein folding accessible to all, Nat Methods, 19, 679, 10.1038/s41592-022-01488-1 · DOI · Paper page
- Nesterova, 2001, Characterization of the genomic xist locus in rodents reveals conservation of overall gene structure and tandem repeats but rapid evolution of unique sequence, Genome Res, 11, 833, 10.1101/gr.174901 · DOI
- Quinodoz, 2022, Essential roles for RNA in shaping nuclear organization, Cold Spring Harb Perspect Biol, 14, a039719, 10.1101/cshperspect.a039719 · DOI
- Quinodoz, 2021, RNA promotes the formation of spatial compartments in the nucleus, Cell, 184, 5775, 10.1016/j.cell.2021.10.014 · DOI
- Broad, 2020, Aurora B kinase is recruited to multiple discrete kinetochore and centromere regions in human cells, J Cell Biol, 219, e201905144, 10.1083/jcb.201905144 · DOI
- Heald, 1990, Mutations of phosphorylation sites in lamin A that prevent nuclear lamina disassembly in mitosis, Cell, 61, 579, 10.1016/0092-8674(90)90470-Y · DOI
- Peter, 1990, In vitro disassembly of the nuclear lamina and M phase-specific phosphorylation of lamins by cdc2 kinase, Cell, 61, 591, 10.1016/0092-8674(90)90471-P · DOI
- Ward, 1990, Identification of cell cycle-regulated phosphorylation sites on nuclear lamin C, Cell, 61, 561, 10.1016/0092-8674(90)90469-U · DOI
- Smith, 2005, Overexpression of aurora B kinase (AURKB) in primary non-small cell lung carcinoma is frequent, generally driven from one allele, and correlates with the level of genetic instability, Br J Cancer, 93, 719, 10.1038/sj.bjc.6602779 · DOI
- Zhang, 2015, Elevated Aurora B expression contributes to chemoresistance and poor prognosis in breast cancer, Int J Clin Exp Pathol, 8, 751
- Chieffi, 2006, Aurora B expression directly correlates with prostate cancer malignancy and influence prostate cell proliferation, Prostate, 66, 326, 10.1002/pros.20345 · DOI
- González-Loyola, 2015, Aurora B overexpression causes aneuploidy and p21Cip1 repression during tumor development, Mol Cell Biol, 35, 3566, 10.1128/MCB.01286-14 · DOI
- Nishibe, 2013, CIZ1, a p21Cip1/Waf1-interacting protein, functions as a tumor suppressor in vivo, FEBS Lett, 587, 1529, 10.1016/j.febslet.2013.03.034 · DOI
- Liu, 2015, Ciz1 promotes tumorigenicity of prostate carcinoma cells, Front Biosci, 20, 705, 10.2741/4331 · DOI
- Higgins, 2012, Variant Ciz1 is a circulating biomarker for early-stage lung cancer, Proc Natl Acad Sci USA, 109, E3128, 10.1073/pnas.1210107109 · DOI
- Wang, 2014, Ciz1 is a novel predictor of survival in human colon cancer, Exp Biol Med (Maywood), 239, 862, 10.1177/1535370213520113 · DOI
- Chen, 2019, CIZ1 knockdown suppresses the proliferation of bladder cancer cells by inducing apoptosis, Gene, 719, 143946, 10.1016/j.gene.2019.143946 · DOI
Metadata
- Authors
- Byrom, L., Turvey, G. L., Dowle, A. A., Thomas, M., Shirodkar, N., Green, B. J., Brown, M., Ball, C., Chapman, K. E., Guglielmi, E., Dickson, W., Noon, E., Sofi, S., Ainscough, J. F.-X., Antson, A. A., & Coverley, D.
- Affiliations
- University of York (GB)
- Mammalian cell cycle research group, Department of Biology, University of York, York , YO10 5DD ,
- Corresponding author
- Byrom, Lewis
- Coverley, Dawn
- ORCID
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2026-01-22
- Volume
- 54
- Issue
- 3
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- PMC
- PMC12862363
- OpenAlex
- W7127184437
- Cited by
- 2
- References
- 1
- Citations by year
- 2026: 2
- FWCI
- 4.10
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Nucleic Acids Research (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (submittedVersion)
- Funders
- Engineering and Physical Sciences Research Council (EP/K039660/1, EP/M028127/1)
- BBSRC (BB/T007222/1)
- Royal Society Leverhulme Trust (SRF\R1\191028)
- Wellcome Trust (224665)
- Medical Research Council (MR/V029088/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- CIZ1, Aurora B kinase, inactive X chromosome, mitosis, prometaphase, RNA-protein interactions, chromatin, nuclear matrix, epigenetic stability, protein phosphorylation, phosphomimetic mutations
- MeSH terms
- Animals, Chromatin, Humans, Mitosis, Nuclear Proteins, X Chromosome, RNA-Binding Proteins, Nuclear Matrix-Associated Proteins, X Chromosome Inactivation, Mice, RNA, Long Noncoding, Aurora Kinase B
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