Cited by 2Genomics and Chromatin DynamicsGenetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesNuclear Structure and Function

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AURKB-driven dissolution of CIZ1–RNA assemblies from the inactive X chromosome in mitosis

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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.

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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
Venue
Nucleic Acids Research
Published
2026-01-22
Volume
54
Issue
3
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W7127184437
Cited by
2
References
1
Citations by year
2026: 2
FWCI
4.10
Type
journal article
Language
en
Open access
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

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