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The ratio between centromeric proteins CENP-A and CENP-C maintains homeostasis of human centromeres

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471143030.cb0808s55openalex-snapshot

Analysis of Protein Turnover by Quantitative SNAP‐Based Pulse‐Chase Imaging

inferredcites →https://doi.org/10.1006/jmbi.1995.0606openalex-snapshot

Mechanism of Protein Access to Specific DNA Sequences in Chromatin: A Dynamic Equilibrium Model for Gene Regulation

inferredcites →https://doi.org/10.1007/978-1-4939-0888-2_34openalex-snapshot

Tracking Histone Variant Nucleosomes Across the Human Cell Cycle Using Biophysical, Biochemical, and Cytological Analyses

inferredcites →https://doi.org/10.1007/bf00328227openalex-snapshot

Identification of a family of human centromere proteins using autoimmune sera from patients with scleroderma

inferredcites →https://doi.org/10.1007/bf00364017openalex-snapshot

Electron microscopy of whole mount metaphase chromosomes

inferredcites →https://doi.org/10.1007/s004120050320openalex-snapshot

A new look at kinetochore structure in vertebrate somatic cells using high-pressure freezing and freeze substitution

inferredcites →https://doi.org/10.1016/0014-4827(78)90480-9openalex-snapshot

Cytochemistry of kinetochores under electron microscopy*1

inferredcites →https://doi.org/10.1016/0092-8674(82)90147-7openalex-snapshot

Yeast centromere DNA is in a unique and highly ordered structure in chromosomes and small circular minichromosomes

inferredcites →https://doi.org/10.1016/j.bpj.2019.03.021openalex-snapshot

The Oligomerization Landscape of Histones

inferredcites →https://doi.org/10.1016/j.ceb.2011.11.003openalex-snapshot

Structural organization of the kinetochore–microtubule interface

inferredcites →https://doi.org/10.1016/j.ceb.2019.02.003openalex-snapshot

Dynamic chromatin organization without the 30-nm fiber

inferredcites →https://doi.org/10.1016/j.cell.2006.09.039openalex-snapshot

The Conserved KMN Network Constitutes the Core Microtubule-Binding Site of the Kinetochore

inferredcites →https://doi.org/10.1016/j.cell.2009.04.049openalex-snapshot

Centromeric Nucleosomes Induce Positive DNA Supercoils

inferredcites →https://doi.org/10.1016/j.cell.2012.05.035openalex-snapshot

Cell-Cycle-Dependent Structural Transitions in the Human CENP-A Nucleosome In Vivo

inferredcites →https://doi.org/10.1016/j.celrep.2015.09.039openalex-snapshot

DNA Topology and Global Architecture of Point Centromeres

inferredcites →https://doi.org/10.1016/j.cub.2011.08.056openalex-snapshot

Endogenous Transcription at the Centromere Facilitates Centromere Activity in Budding Yeast

inferredcites →https://doi.org/10.1016/j.cub.2013.03.037openalex-snapshot

Octameric CENP-A Nucleosomes Are Present at Human Centromeres throughout the Cell Cycle

inferredcites →https://doi.org/10.1016/j.cub.2016.02.061openalex-snapshot

Long-Term Retention of CENP-A Nucleosomes in Mammalian Oocytes Underpins Transgenerational Inheritance of Centromere Identity

inferredcites →https://doi.org/10.1016/j.devcel.2017.07.001openalex-snapshot

Human Centromeres Produce Chromosome-Specific and Array-Specific Alpha Satellite Transcripts that Are Complexed with CENP-A and CENP-C

inferredcites →https://doi.org/10.1016/j.febslet.2012.09.012openalex-snapshot

Structural features of human histone acetyltransferase p300 and its complex with p53

inferredcites →https://doi.org/10.1016/j.gde.2005.01.004openalex-snapshot

Centromeric chromatin: what makes it unique?

inferredcites →https://doi.org/10.1016/j.molcel.2014.01.018openalex-snapshot

Mislocalization of the Centromeric Histone Variant CenH3/CENP-A in Human Cells Depends on the Chaperone DAXX

inferredcites →https://doi.org/10.1016/j.molcel.2016.06.023openalex-snapshot

The Flexible Ends of CENP-A Nucleosome Are Required for Mitotic Fidelity

inferredcites →https://doi.org/10.1016/j.sbi.2016.03.003openalex-snapshot

Progress in the structural and functional characterization of kinetochores

inferredcites →https://doi.org/10.1016/j.tcb.2011.01.003openalex-snapshot

Merotelic kinetochore attachment: causes and effects

inferredcites →https://doi.org/10.1016/s1534-5807(02)00135-1openalex-snapshot

Conserved Organization of Centromeric Chromatin in Flies and Humans

inferredcites →https://doi.org/10.1021/jacs.6b05355openalex-snapshot

Promiscuous Histone Mis-Assembly Is Actively Prevented by Chaperones

inferredcites →https://doi.org/10.1021/la802452vopenalex-snapshot

Immuno-Atomic Force Microscopy Characterization of Adsorbed Fibronectin

inferredcites →https://doi.org/10.1021/la960918xopenalex-snapshot

Atomic Force Microscopic Study of Specific Antigen/Antibody Binding

inferredcites →https://doi.org/10.1038/emboj.2010.329openalex-snapshot

Epigenetic engineering shows H3K4me2 is required for HJURP targeting and CENP‐A assembly on a synthetic human kinetochore

inferredcites →https://doi.org/10.1038/nature10258openalex-snapshot

Crystal structure of the human centromeric nucleosome containing CENP-A

inferredcites →https://doi.org/10.1038/nature19333openalex-snapshot

Insights from biochemical reconstitution into the architecture of human kinetochores

inferredcites →https://doi.org/10.1038/ncb1397openalex-snapshot

The human CENP-A centromeric nucleosome-associated complex

inferredcites →https://doi.org/10.1038/ncomms15775openalex-snapshot

Centromeres are maintained by fastening CENP-A to DNA and directing an arginine anchor-dependent nucleosome transition

inferredcites →https://doi.org/10.1038/ncomms9161openalex-snapshot

A quantitative description of Ndc80 complex linkage to human kinetochores

inferredcites →https://doi.org/10.1038/nrg.2016.157openalex-snapshot

Chromatin dynamics during the cell cycle at centromeres

inferredcites →https://doi.org/10.1038/nrm.2015.5openalex-snapshot

The molecular basis for centromere identity and function

inferredcites →https://doi.org/10.1038/nsb996openalex-snapshot

Phylogenomics of the nucleosome

inferredcites →https://doi.org/10.1038/nsmb.2358openalex-snapshot

The structure of purified kinetochores reveals multiple microtubule-attachment sites

inferredcites →https://doi.org/10.1038/nsmb.2562openalex-snapshot

The octamer is the major form of CENP-A nucleosomes at human centromeres

inferredcites →https://doi.org/10.1038/nsmb.2742openalex-snapshot

CENP-A octamers do not confer a reduction in nucleosome height by AFM

inferredcites →https://doi.org/10.1038/nsmb.3175openalex-snapshot

CENP-C directs a structural transition of CENP-A nucleosomes mainly through sliding of DNA gyres

inferredcites →https://doi.org/10.1038/nsmb845openalex-snapshot

Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatin

inferredcites →https://doi.org/10.1038/s41576-018-0089-8openalex-snapshot

Chromatin accessibility and the regulatory epigenome

inferredcites →https://doi.org/10.1038/s41586-019-1669-2openalex-snapshot

HP1 reshapes nucleosome core to promote phase separation of heterochromatin

inferredcites →https://doi.org/10.1038/srep17038openalex-snapshot

Shearing of the CENP-A dimerization interface mediates plasticity in the octameric centromeric nucleosome

inferredcites →https://doi.org/10.1039/c6nr06245hopenalex-snapshot

The supercoiling state of DNA determines the handedness of both H3 and CENP-A nucleosomes

inferredcites →https://doi.org/10.1073/pnas.1002325107openalex-snapshot

A super-resolution map of the vertebrate kinetochore

inferredcites →https://doi.org/10.1073/pnas.1009563107openalex-snapshot

Tetrameric organization of vertebrate centromeric nucleosomes

inferredcites →https://doi.org/10.1073/pnas.1118898109openalex-snapshot

Tripartite organization of centromeric chromatin in budding yeast

inferredcites →https://doi.org/10.1073/pnas.1614145114openalex-snapshot

Stepwise unfolding supports a subunit model for vertebrate kinetochores

inferredcites →https://doi.org/10.1073/pnas.1821384116openalex-snapshot

Point centromere activity requires an optimal level of centromeric noncoding RNA

inferredcites →https://doi.org/10.1073/pnas.1911880116openalex-snapshot

Intrinsic elasticity of nucleosomes is encoded by histone variants and calibrated by their binding partners

inferredcites →https://doi.org/10.1073/pnas.85.1.175openalex-snapshot

Chromatin structure of altered yeast centromeres.

inferredcites →https://doi.org/10.1073/pnas.86.16.6250openalex-snapshot

Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA.

inferredcites →https://doi.org/10.1073/pnas.88.9.3734openalex-snapshot

Purification of the centromere-specific protein CENP-A and demonstration that it is a distinctive histone.

inferredcites →https://doi.org/10.1073/pnas.95.3.1136openalex-snapshot

Targeted disruption of mouse centromere protein C gene leads to mitotic disarray and early embryo death

inferredcites →https://doi.org/10.1073/pnas.97.3.1148openalex-snapshot

Early disruption of centromeric chromatin organization in centromere protein A ( Cenpa ) null mice

inferredcites →https://doi.org/10.1074/jbc.m110.189340openalex-snapshot

Biophysical Characterization of the Centromere-specific Nucleosome from Budding Yeast

inferredcites →https://doi.org/10.1074/jbc.m111.228510openalex-snapshot

Identification of Noncoding Transcripts from within CENP-A Chromatin at Fission Yeast Centromeres

inferredcites →https://doi.org/10.1074/jbc.m707344200openalex-snapshot

Nuclear Non-coding RNAs Are Transcribed from the Centromeres of Plasmodium falciparum and Are Associated with Centromeric Chromatin

inferredcites →https://doi.org/10.1074/jbc.ra118.004141openalex-snapshot

Conformational flexibility of histone variant CENP-ACse4 is regulated by histone H4: A mechanism to stabilize soluble Cse4

inferredcites →https://doi.org/10.1074/mcp.m115.053710openalex-snapshot

Identification of the Post-translational Modifications Present in Centromeric Chromatin

inferredcites →https://doi.org/10.1083/jcb.201001013openalex-snapshot

Dual recognition of CENP-A nucleosomes is required for centromere assembly

inferredcites →https://doi.org/10.1083/jcb.201012050openalex-snapshot

Spindle microtubules generate tension-dependent changes in the distribution of inner kinetochore proteins

inferredcites →https://doi.org/10.1083/jcb.201404097openalex-snapshot

Repetitive centromeric satellite RNA is essential for kinetochore formation and cell division

inferredcites →https://doi.org/10.1083/jcb.20140409711122014copenalex-snapshot

Repetitive centromeric satellite RNA is essential for kinetochore formation and cell division

inferredcites →https://doi.org/10.1083/jcb.201412028openalex-snapshot

CENP-C is a blueprint for constitutive centromere–associated network assembly within human kinetochores

inferredcites →https://doi.org/10.1083/jcb.201604029openalex-snapshot

Mitotic noncoding RNA processing promotes kinetochore and spindle assembly in Xenopus

inferredcites →https://doi.org/10.1083/jcb.201611087openalex-snapshot

Centromere transcription allows CENP-A to transit from chromatin association to stable incorporation

inferredcites →https://doi.org/10.1091/mbc.e07-01-0045openalex-snapshot

CENP-C Is Involved in Chromosome Segregation, Mitotic Checkpoint Function, and Kinetochore Assembly

inferredcites →https://doi.org/10.1091/mbc.e09-05-0378openalex-snapshot

Dissection of CENP-C–directed Centromere and Kinetochore Assembly

inferredcites →https://doi.org/10.1091/mbc.e13-01-0034openalex-snapshot

Assembly in G1 phase and long-term stability are unique intrinsic features of CENP-A nucleosomes

inferredcites →https://doi.org/10.1091/mbc.e18-12-0799openalex-snapshot

In vitro BioID: mapping the CENP-A microenvironment with high temporal and spatial resolution

inferredcites →https://doi.org/10.1093/emboj/18.15.4196openalex-snapshot

CENP‐C is necessary but not sufficient to induce formation of a functional centromere

inferredcites →https://doi.org/10.1093/genetics/157.3.1293openalex-snapshot

Adaptive Evolution of Cid, a Centromere-Specific Histone in Drosophila

inferredcites →https://doi.org/10.1093/molbev/msh179openalex-snapshot

Adaptive Evolution of the Histone Fold Domain in Centromeric Histones

inferredcites →https://doi.org/10.1093/nar/gkp529openalex-snapshot

Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinase

inferredcites →https://doi.org/10.1093/nar/gks921openalex-snapshot

Transcription in the maintenance of centromere chromatin identity

inferredcites →https://doi.org/10.1093/nar/gkt314openalex-snapshot

Reconstitution of hemisomes on budding yeast centromeric DNA

inferredcites →https://doi.org/10.1093/nar/gkx933openalex-snapshot

Nanoscale dynamics of centromere nucleosomes and the critical roles of CENP-A

inferredcites →https://doi.org/10.1098/rstb.2004.1610openalex-snapshot

Merotelic kinetochores in mammalian tissue cells

inferredcites →https://doi.org/10.1101/cshperspect.a015826openalex-snapshot

The Kinetochore

inferredcites →https://doi.org/10.1101/gr.3810906openalex-snapshot

The evolutionary dynamics of α-satellite

inferredcites →https://doi.org/10.1101/gr.6022807openalex-snapshot

Centromere RNA is a key component for the assembly of nucleoproteins at the nucleolus and centromere

inferredcites →https://doi.org/10.1111/j.1365-2184.1977.tb00309.xopenalex-snapshot

CELL CYCLE CHARACTERISTICS OF SYNCHRONIZED AND ASYNCHRONOUS POPULATIONS OF HUMAN CELLS AND EFFECT OF COOLING OF SELECTED MITOTIC CELLS

inferredcites →https://doi.org/10.1126/sciadv.1400234openalex-snapshot

A unique chromatin complex occupies young α-satellite arrays of human centromeres

inferredcites →https://doi.org/10.1126/science.1062939openalex-snapshot

The Centromere Paradox: Stable Inheritance with Rapidly Evolving DNA

inferredcites →https://doi.org/10.1126/science.1206880openalex-snapshot

Drosophila CENH3 Is Sufficient for Centromere Formation

inferredcites →https://doi.org/10.1126/science.1235532openalex-snapshot

A Conserved Mechanism for Centromeric Nucleosome Recognition by Centromere Protein CENP-C

inferredcites →https://doi.org/10.1126/science.1259308openalex-snapshot

CENP-C reshapes and stabilizes CENP-A nucleosomes at the centromere

inferredcites →https://doi.org/10.1128/mcb.25.10.3967-3981.2005openalex-snapshot

CENP-A Is Required for Accurate Chromosome Segregation and Sustained Kinetochore Association of BubR1

inferredcites →https://doi.org/10.1146/annurev-biophys-070317-032847openalex-snapshot

Biophysics of Chromatin Dynamics

inferredcites →https://doi.org/10.1146/annurev.biophys.27.1.285openalex-snapshot

STRUCTURE, DYNAMICS, AND FUNCTION OF CHROMATIN IN VITRO

inferredcites →https://doi.org/10.1159/000130113openalex-snapshot

Whole-mount electron microscopy of the centromere region of metacentric and telocentric mammalian chromosomes

inferredcites →https://doi.org/10.1186/1756-8935-1-10openalex-snapshot

Single-epitope recognition imaging of native chromatin

inferredcites →https://doi.org/10.1186/1756-8935-8-2openalex-snapshot

CENP-A nucleosomes localize to transcription factor hotspots and subtelomeric sites in human cancer cells

inferredcites →https://doi.org/10.1186/gb-2006-7-3-r23openalex-snapshot

Phylogenetic and structural analysis of centromeric DNA and kinetochore proteins

inferredcites →https://doi.org/10.1186/gb-2013-14-1-r10openalex-snapshot

Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution

inferredcites →https://doi.org/10.1186/jbiol11openalex-snapshot

Adaptive evolution of centromere proteins in plants and animals

inferredcites →https://doi.org/10.1186/s13072-017-0124-6openalex-snapshot

Internal modifications in the CENP-A nucleosome modulate centromeric dynamics

inferredcites →https://doi.org/10.1186/s13072-018-0185-1openalex-snapshot

Histone H3K9 and H4 Acetylations and Transcription Facilitate the Initial CENP-AHCP−3 Deposition and De Novo Centromere Establishment in Caenorhabditis elegans Artificial Chromosomes

inferredcites →https://doi.org/10.1186/s13072-018-0237-6openalex-snapshot

High-resolution mapping of centromeric protein association using APEX-chromatin fibers

inferredcites →https://doi.org/10.1371/journal.pbio.0050218openalex-snapshot

Tetrameric Structure of Centromeric Nucleosomes in Interphase Drosophila Cells

inferredcites →https://doi.org/10.1371/journal.pgen.1000354openalex-snapshot

LINE Retrotransposon RNA Is an Essential Structural and Functional Epigenetic Component of a Core Neocentromeric Chromatin

inferredcites →https://doi.org/10.1371/journal.pgen.1004970openalex-snapshot

Naturally Occurring Differences in CENH3 Affect Chromosome Segregation in Zygotic Mitosis of Hybrids

inferredcites →https://doi.org/10.1371/journal.pgen.1004986openalex-snapshot

Sequence Features and Transcriptional Stalling within Centromere DNA Promote Establishment of CENP-A Chromatin

inferredcites →https://doi.org/10.1371/journal.pone.0000478openalex-snapshot

Molecular Analysis of Core Kinetochore Composition and Assembly in Drosophila melanogaster

inferredcites →https://doi.org/10.1371/journal.pone.0006564openalex-snapshot

Multipolar Spindle Pole Coalescence Is a Major Source of Kinetochore Mis-Attachment and Chromosome Mis-Segregation in Cancer Cells

inferredcites →https://doi.org/10.1371/journal.pone.0165078openalex-snapshot

CENP-A and H3 Nucleosomes Display a Similar Stability to Force-Mediated Disassembly

inferredcites →https://doi.org/10.1371/journal.pone.0205948openalex-snapshot

HJURP antagonizes CENP-A mislocalization driven by the H3.3 chaperones HIRA and DAXX

inferredcites →https://doi.org/10.15252/embr.201948913openalex-snapshot

CENP‐C unwraps the human CENP‐A nucleosome through the H2A C‐terminal tail

inferredcites →https://doi.org/10.3390/genes6030751openalex-snapshot

Chromatin Dynamics in Vivo: A Game of Musical Chairs

inferredcites →https://doi.org/10.4161/nucl.23588openalex-snapshot

The CENP-A nucleosome

inferredcites →https://doi.org/10.7554/elife.01861openalex-snapshot

The budding yeast Centromere DNA Element II wraps a stable Cse4 hemisome in either orientation in vivo

inferredcites →https://doi.org/10.7554/elife.02137openalex-snapshot

The quantitative architecture of centromeric chromatin

inferredcites →https://doi.org/10.7554/elife.03254openalex-snapshot

A long non-coding RNA is required for targeting centromeric protein A to the human centromere

inferredcites →https://doi.org/10.7554/elife.09225openalex-snapshot

A simple method for generating high-resolution maps of genome-wide protein binding

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1038/s41580-020-0262-8openalex-snapshot

The roles of histone variants in fine-tuning chromatin organization and function

inferred← citeshttps://doi.org/10.1073/pnas.1911880116openalex-snapshot

Intrinsic elasticity of nucleosomes is encoded by histone variants and calibrated by their binding partners

inferred← citeshttps://doi.org/10.70675/123360c5z2402z4edcz8d5ezddeb1b30f62eopenalex-snapshot

A genetic memory initiates the epigenetic loop necessary to preserve centromere position

inferred← citeshttps://doi.org/10.7554/elife.59770openalex-snapshot

Alpha-satellite RNA transcripts are repressed by centromere–nucleolus associations

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