| 2006 |
CENP-A nucleosomes directly recruit a proximal nucleosome-associated complex (NAC) comprising CENP-M, CENP-N, CENP-T, CENP-U(50), CENP-C, and CENP-H. Assembly of the NAC requires CENP-M, CENP-N, and CENP-T. FACT and nucleophosmin-1 are stably recruited to CENP-A nucleosomes independently of the NAC. Seven distal CAD components (CENP-K, -L, -O, -P, -Q, -R, -S) assemble on the NAC. Disruption of the NAC causes chromosome alignment and segregation errors. |
Mass spectrometry, co-immunoprecipitation, RNAi depletion with mitotic phenotype readout |
Nature cell biology |
High |
16622419
|
| 2000 |
Cenpa null mouse embryos fail to survive beyond E6.5 with severe mitotic defects. Cenpa is required for kinetochore targeting of Cenpc; loss of Cenpa causes diffuse Cenpb foci and complete loss of discrete Cenpc centromere signal, indicating Cenpa organizes centromeric chromatin and is epistatic to Cenpc localization. |
Gene targeting (knockout mouse), immunofluorescence microscopy |
Proceedings of the National Academy of Sciences of the United States of America |
High |
10655499
|
| 2011 |
Crystal structure of HJURP bound to a CENP-A–H4 heterodimer shows HJURP binds a pre-nucleosomal CENP-A–H4 heterodimer; the C-terminal β-sheet domain of HJURP caps the DNA-binding surface of CENP-A–H4, preventing spontaneous DNA association. A novel CENP-A-specific surface distinguishes it from H3 in HJURP binding. |
X-ray crystallography, in vitro binding assays |
Genes & development |
High |
21478274
|
| 2015 |
CENP-C binds CENP-A nucleosomes and reshapes the octameric histone core: it rigidifies both surface and internal nucleosome structure and modulates terminal DNA to match the loose DNA wrap characteristic of native centromeric CENP-A nucleosomes. CENP-C depletion leads to rapid removal of CENP-A from centromeres, demonstrating collaboration between CENP-C and CENP-A in maintaining centromere identity. |
Purified-component reconstitution, FRET, single-molecule PIFE, auxin-inducible degron depletion |
Science (New York, N.Y.) |
High |
25954010
|
| 2014 |
Polo-like kinase 1 (Plk1) is required to initiate CENP-A deposition in human cells by promoting localization of the Mis18 complex to centromeres. CDK inhibits Mis18 complex assembly. A two-step Plk1/CDK regulatory paradigm controls cell-cycle-restricted CENP-A deposition; bypassing both steps uncouples deposition from cell-cycle progression and causes mitotic defects. |
RNAi/chemical inhibition, FRAP, auxin-inducible degron, epistasis with phosphomutants |
Cell |
High |
25036634
|
| 2014 |
Cdk1 phosphorylates CENP-A at Ser68 during early mitosis, which eliminates binding of CENP-A to its assembly chaperone HJURP, thereby preventing premature centromeric loading before mitotic exit. PP1α dephosphorylates Ser68 at mitotic exit, enabling HJURP-mediated centromeric deposition. |
In vitro kinase assay, phosphomutant rescue, co-immunoprecipitation, cell synchronization |
Developmental cell |
High |
25556658
|
| 2015 |
CUL4A-RBX1-COPS8 E3 ligase monoubiquitylates CENP-A on K124, which is required for CENP-A interaction with chaperone HJURP and for centromere localization. The K124R mutation reduces HJURP binding and abolishes centromere loading; addition of monoubiquitin to K124R restores both HJURP interaction and centromere localization. |
In vitro ubiquitylation assay, co-immunoprecipitation, CRISPR knockin, immunofluorescence |
Developmental cell |
High |
25727006
|
| 2018 |
HJURP transiently associates with pre-existing CENP-A nucleosomes during S phase and is required for CENP-A nucleosome inheritance through DNA replication. HJURP co-purifies with the MCM2-7 helicase complex, and MCM2 and HJURP simultaneously bind CENP-A, defining a mechanism for retaining CENP-A during replication fork passage. |
BioID proximity labeling, co-immunoprecipitation, conditional depletion (auxin), quantitative imaging |
Developmental cell |
High |
30293838
|
| 2022 |
Cryo-EM structures of the human inner kinetochore CCAN complex bound to a CENP-A nucleosome reconstituted on α-satellite DNA show that CCAN forms edge-on contacts with the CENP-A nucleosome; a linker DNA segment threads through the central CENP-LN channel; CENP-TWSX partially wraps linker DNA. This topological entrapment of linker DNA by CCAN provides a mechanism for kinetochores to withstand spindle forces. |
Cryo-electron microscopy, reconstitution of CENP-A nucleosome on α-satellite DNA |
Science (New York, N.Y.) |
High |
35420891
|
| 2016 |
Cell-cycle control of CENP-A assembly requires two targets: a single Cdk phosphorylation site in licensing factor M18BP1 and a cyclin A binding site in HJURP. Simultaneous mutation of both sites completely uncouples CENP-A assembly from cell-cycle phase, allowing assembly under high Cdk activity indistinguishable from G1 assembly. Cdk-mediated inhibition works by sequestering active factors away from the centromere. |
Phosphomutant expression, quantitative live-cell imaging, CENP-A incorporation assays, cell-cycle staging |
Molecular cell |
High |
28017591
|
| 2005 |
In CENP-A-depleted chicken DT40 cells, inner kinetochore proteins CENP-I, CENP-H, and CENP-C and outer components Nuf2/Hec1, Mad2, and CENP-E are mislocalised, whereas BubR1 and INCENP are efficiently recruited. CENP-A-depleted cells show chromosome congression defects and a specific defect in maintaining BubR1 at kinetochores under checkpoint activation, indicating CENP-A is required for a mitotic-checkpoint-competent kinetochore. |
Conditional gene disruption (DT40), immunofluorescence, epistasis of kinetochore component localization |
Molecular and cellular biology |
High |
15870271
|
| 2001 |
CENP-A is phosphorylated at a serine residue (equivalent to H3 Ser10) in a cell-cycle-dependent manner distinct from histone H3. CENP-A phosphorylation begins in prophase, peaks in prometaphase, and disappears in telophase—after both pericentric and genome-wide H3 phosphorylation. Prekinetochore duplication (CENP-A foci doubling) occurs before complete H3 phosphorylation in G2. |
Phospho-specific antibody ELISA, western blot, quantitative immunocytochemistry |
Journal of cell science |
Medium |
11171370
|
| 2009 |
CENP-A is rapidly recruited to DNA double-strand breaks (DSBs) in human and mouse cells, along with centromere-associated proteins CENP-N, CENP-T, and CENP-U. The centromere-targeting domain (CATD) of CENP-A is necessary and sufficient for recruitment to DSBs. CENP-A accumulation at breaks is enhanced by active NHEJ but does not require DNA-PKcs, Ligase IV, or H2AX. |
Multiphoton laser microirradiation, I-SceI endonuclease-induced DSBs, CENP-A domain truncation/mutation, immunofluorescence |
Proceedings of the National Academy of Sciences of the United States of America |
Medium |
19717431
|
| 2014 |
CENP-A overexpression leads to ectopic enrichment at sites of active histone turnover in a heterotypic CENP-A/H3.3–H4 tetramer. Ectopic localization depends on H3.3 chaperone DAXX rather than the dedicated CENP-A chaperone HJURP. Ectopic CENP-A nucleosomes occlude CTCF binding and confer DNA damage tolerance, both dependent on DAXX. |
ChIP-seq, co-immunoprecipitation, RNAi knockdown, CTCF binding assay, cell survival assay |
Molecular cell |
High |
24530302
|
| 2012 |
Human CENP-A nucleosomes undergo cell-cycle-dependent structural transitions in vivo: they exist as tetramers (half-nucleosomes) after replication and convert to octamers before the next replication, accompanied by reversible chaperone binding, chromatin fiber folding changes, and histone fold domain modifications on CENP-A and H4. |
AFM, mass spectrometry of PTMs, chromatin fractionation, cell-cycle synchronization |
Cell |
Medium |
22817894
|
| 2017 |
Human centromeric CENP-A chromatin is exclusively an octameric nucleosome at all cell-cycle phases (G1 and G2), containing equimolar CENP-A, H2A, H2B, and H4 with no H3. CENP-A nucleosomes protect DNA lengths centered on 133 bp, consistent with octamers with DNA unwrapping at entry and exit. Solid-state nanopore analyses confirm nucleosomal size. |
ChIP-seq with new reference models, MNase protection assay, nanopore analysis, quantitative mass spectrometry |
The Journal of cell biology |
High |
28235947
|
| 2019 |
Cryo-EM structures of centromeric tri-nucleosomes show that H3-CENP-A-H3 tri-nucleosomes adopt an untwisted architecture with outward-facing linker DNA path between nucleosomes, distinct from H3-H3-H3 tri-nucleosomes with inward-facing DNA. This exposes the CENP-A nucleosome to solvent in condensed chromatin. |
Cryo-electron microscopy, tri-nucleosome reconstitution |
Structure (London, England : 1993) |
High |
31711756
|
| 2018 |
Aurora A kinase phosphorylates CENP-A at serine 7 (S7) at inner centromeres in mitosis, protecting bioriented chromosomes against cohesion fatigue. Expression of non-phosphorylatable CENP-A S7A weakens sister chromatid cohesion only when centromeres are under spindle tension. Aurora A is recruited to centromeres in a Bub1-dependent manner. |
Phosphomutant CENP-A expression, chromosome cohesion assays, Aurora A inhibition, immunofluorescence |
Nature communications |
Medium |
29760389
|
| 2019 |
Phosphorylation of CENP-A on serine 7 is dispensable for correct CENP-C recruitment, faithful chromosome segregation, and long-term cell viability, as demonstrated by gene targeting at both endogenous CENP-A alleles and gene replacement with S7A in human cells. |
Gene targeting at endogenous loci (CRISPR), gene replacement, immunofluorescence, live-cell imaging |
Nature communications |
High |
30635586
|
| 2019 |
CENP-C unwraps the human CENP-A nucleosome through the H2A C-terminal tail. The CENP-C central region (CENP-C_CR) binds the CENP-A nucleosome with high affinity via an extended hydrophobic area involving CENP-A V532 and V533. CENP-C binding further loosens terminal DNA wrapping (through H2A C-tail destabilization) and rigidifies the H4 N-terminal tail in a conformation favoring H4K20 monomethylation. |
Cryo-EM, in vitro binding assays, nucleosome reconstitution, mutagenesis |
EMBO reports |
High |
31475439
|
| 2019 |
CDK1 phosphorylates CENP-C in its C-terminal CENP-A binding motif, which facilitates CENP-C binding to the CENP-A nucleosome in vitro and in vivo. This phosphorylation promotes CENP-C kinetochore localization during mitosis. The CENP-A–CENP-C interaction is critical for long-term cell viability in human RPE-1 cells. |
In vitro kinase assay, co-immunoprecipitation, phosphomutant rescue, immunofluorescence, cell viability assays |
The Journal of cell biology |
High |
31676716
|
| 2015 |
CENP-B forms a stable complex with the CENP-A nucleosome in vitro, preferentially when the CENP-B box DNA is located at the proximal edge of the nucleosome. The CENP-B DNA-binding domain specifically interacts with the CENP-A–H4 complex (but not H3.1–H4). In vivo, CENP-B binding near the CENP-A nucleosome substantially stabilizes CENP-A on alphoid DNA. |
In vitro nucleosome reconstitution, pulldown assay, in vivo chromatin stability assay |
Nucleic acids research |
High |
25916850
|
| 2018 |
Centromeric transcription by RNA Pol II temporally coincides with de novo dCENP-A deposition in Drosophila. Short inhibition of transcription impairs CENP-A incorporation into stable (salt-resistant) chromatin but does not prevent initial targeting to centromeres, revealing two stability states of newly loaded CENP-A: a salt-sensitive association and a salt-resistant incorporated form. Transcription-mediated chromatin remodeling drives the transition to fully incorporated nucleosomes. |
Drosophila tissue culture, transcription inhibitor treatment, SNAP-tag pulse-chase, chromatin fractionation |
The Journal of cell biology |
High |
29626011
|
| 2020 |
Spt6, a histone chaperone and transcription elongation factor, prevents loss of old CENP-A nucleosomes during centromeric transcription. Spt6 directly binds dCENP-A in vitro; phosphomimetic dCENP-A mutants reduce Spt6 association, and non-phosphorylatable dCENP-A accumulates at centromeres. Spt6 acts as a conserved CENP-A maintenance factor in both Drosophila and human cells. |
Co-immunoprecipitation/direct binding assay, SNAP-tag pulse-chase, phosphomutant analysis, immunofluorescence |
Nature communications |
High |
32522980
|
| 2021 |
CENP-A chromatin protects centromeric alpha-satellite DNA from replication stress during S phase. Rapid CENP-A removal specifically in S phase causes R-loop accumulation with increased centromeric transcripts, impaired replication fork progression, recombination at alpha-satellites, and anaphase bridges leading to chromosome breakage and translocations at centromeric regions. |
Auxin-inducible degron for cell-cycle-specific CENP-A removal, DNA-RNA immunoprecipitation, DNA fiber assay, cytogenetics |
Proceedings of the National Academy of Sciences of the United States of America |
High |
33653953
|
| 2016 |
CENP-A ubiquitylation (K124) is inherited between cell divisions through CENP-A dimerization. Pre-existing ubiquitylated CENP-A is necessary for recruitment of newly synthesized CENP-A to the centromere. In vivo and in vitro experiments with dimerization mutants show that inheritance of K124 ubiquitylation requires CENP-A dimerization. Overexpression of monoubiquitin-fused CENP-A induces neocentromeres at non-centromeric regions. |
In vivo and in vitro dimerization mutant analysis, co-immunoprecipitation, immunofluorescence, ectopic CENP-A expression |
Cell reports |
Medium |
27052173
|
| 2019 |
CENP-A HJURP nucleosome clusters form rosette-like structures (~250–300 nm) around HJURP during G1 phase. 2D/3D super-resolution microscopy shows HJURP localizes to the center of these rosettes and acts as a nucleation point for CENP-A deposition, providing structural insight into centromeric chromatin organization during loading. |
Super-resolution microscopy (STORM/PALM), co-localization analysis, segmentation |
Nature communications |
Medium |
31570711
|
| 2014 |
Cell-cycle-dependent recruitment of HJURP to centromeres depends on timely CDK-mediated phosphorylation of HJURP. A non-phosphorylatable HJURP mutant localizes prematurely to centromeres in S and G2, causing premature CENP-A loading and cell-cycle delays. Once at centromeres, HJURP promotes CENP-A deposition through a unique DNA-binding domain. |
Phosphomutant expression, cell-cycle synchronization, immunofluorescence, DNA binding assays |
Cell reports |
High |
25001279
|
| 2015 |
In a cell-free CENP-A assembly system, two distinct domains of CENP-A within existing nucleosomes are required for new CENP-A assembly. CENP-A nucleosomes recruit CENP-C and M18BP1 independently, and CENP-C recruitment depends on the density of underlying CENP-A nucleosomes. |
Cell-free CENP-A assembly system (Xenopus extract), domain truncation analysis, chromatin binding assays |
The Journal of cell biology |
High |
26076692
|
| 2017 |
At yeast centromeres, Cse4/CENP-A histone-fold domain interacts with inner kinetochore protein Mif2/CENP-C. Mif2 contacts one side of the nucleosome dyad engaging both Cse4 residues and AT-rich centromeric DNA through a contiguous DNA- and histone-binding domain (DHBD) containing the CENP-C motif, an AT hook, and RK clusters. Human CENP-C has two related DHBDs with preference for AT-rich DNA. |
Biochemical binding assays, mutagenesis, ChIP, structural modeling |
Genes & development |
High |
29074736
|
| 2002 |
PARP-2 co-immunoprecipitates with CENP-A (Cenpa) and CENP-B (Cenpb) at active centromeres in a cell-cycle-dependent manner (accumulating prometaphase/metaphase, disassociating by telophase). PARP-2 does not interact with CENP-C. PARP-2 centromere binding is sequence-independent and enhanced by microtubule-inhibiting drugs. |
Co-immunoprecipitation, immunofluorescence, pseudodicentric chromosome analysis |
Human molecular genetics |
Medium |
12217960
|
| 2012 |
In Saccharomyces cerevisiae, Cse4/CENP-A (centromeric H3 variant) is methylated on arginine 37 (R37). Absence of R37 methylation reduces levels of Mtw1/MIND and Ctf19 complex components at the centromere (but not Cse4 itself), causing growth defects, G2/M arrest, and chromosome segregation errors. This modification regulates recruitment of linker kinetochore components. |
Mass spectrometry, methylation mutants, genetic epistasis with kinetochore mutants, ChIP |
Proceedings of the National Academy of Sciences of the United States of America |
Medium |
22615363
|
| 2017 |
CENPT bridges adjacent CENPA nucleosomes on young human α-satellite dimers. Sequential ChIP-seq shows CENPT is centered between two well-positioned CENPA nucleosomes over the CENPB box, forming a CENPA/CENPB/CENPC/CENPT complex nuclease-protected over an α-satellite dimer. CENPT interacts with CENPB/CENPC complex rather than H3 nucleosomes in vivo. |
Comparative and sequential ChIP-seq, base-pair-resolution genomic readout of protein-protein interactions |
Genome research |
Medium |
27384170
|
| 2024 |
CENP-A functions as an m6A reader of centromeric RNA (cenRNA): m6A-modified cenRNA stabilizes centromeric localization of CENP-A during S phase. Mutations at CENP-A Leu61 and Arg63 abolish cenRNA binding and cause loss of centromere-bound CENP-A during S phase, compromised centromere integrity, and abnormal chromosome separation. |
m6A methylation mapping, CENP-A mutagenesis, RNA-protein binding assays, live-cell imaging, tumor xenograft |
Cell |
High |
39305902
|
| 2021 |
CENP-A overexpression causes CIN with lagging chromosomes and micronuclei due to reduced localization of kinetochore proteins, resulting in defective kinetochore integrity and unstable kinetochore-microtubule attachments. CENP-A OE also reduces cell adhesion gene expression and increases invasion. |
Inducible overexpression, kinetochore protein quantification by immunofluorescence, live-cell imaging, xenograft |
The Journal of cell biology |
Medium |
33620383
|
| 2021 |
CENPA overexpression promotes prostate cancer cell growth through a non-centromeric function as a transcriptional regulator that modulates expression of proliferation, cell-cycle, and centromere/kinetochore genes, as revealed by integrated ChIP-seq and RNA-seq experiments. |
ChIP-seq, RNA-seq, gain/loss-of-function experiments, tissue microarray |
The Journal of biological chemistry |
Medium |
32371391
|
| 2021 |
CENPA recruits histone acetyltransferase GCN-5 to the promoter of KPNA2 to induce transcription activation in colon cancer cells. This non-centromeric transcriptional activity of CENPA promotes glycolysis and growth. H3K27ac modification is detected at the KPNA2 promoter upon CENPA binding. |
ChIP assay, co-immunoprecipitation, RNAi knockdown, rescue experiments, metabolic assays |
The American journal of pathology |
Medium |
34508688
|
| 2021 |
Phosphorylation of CENP-A Ser68 primes polyubiquitin-mediated proteasomal degradation of CENP-A during mitotic phase. DCAF11 (WDR23) is the E3 ligase mediating this polyubiquitination via K49 and K124. Mutation of K49R/K124R or DCAF11 deletion abrogates proper degradation and causes CENP-A mislocalization. |
In vivo ubiquitination assay, proteasome inhibitor treatment, DCAF11 depletion/knockout, immunofluorescence |
Cell reports |
Medium |
34758320
|
| 2023 |
HJURP phosphorylation by CDK prevents HJURP interaction with CENP-C in metaphase, blocking delivery of soluble CENP-A to centromeres. Non-phosphorylatable HJURP constitutively binds CENP-C in metaphase but is insufficient for new CENP-A assembly. M18BP1.S subunit of the Mis18 complex competitively inhibits HJURP access to CENP-C. Two inhibitory activities together repress CENP-A assembly in metaphase. |
X. laevis egg extract cell-free assembly system, phosphomutant analysis, co-immunoprecipitation, competitive binding assays |
The Journal of cell biology |
High |
37141119
|
| 2023 |
Cryo-EM structure of chicken CENP-A nucleosome bound to ggKNL2 (Mis18 complex component with CENP-C-like motif) shows ggKNL2 simultaneously recognizes the CENP-A C-terminal tail and the RG-loop using its CENP-C-like motif to distinguish CENP-A from H3. ggKNL2 changes its centromere binding partner during cell cycle progression. |
Cryo-EM structure, biochemical binding assays, cell biology validation, cell-cycle analysis |
The EMBO journal |
High |
36744604
|
| 2023 |
CENP-A and CENP-B collaborate to establish an open centromeric chromatin state. CENP-A incorporation increases chromatin fiber dynamics. This increased dynamics allow CENP-B DNA access; bound CENP-B further opens chromatin fiber structure and induces nucleosomal DNA unwrapping. Removal of CENP-A increases CENP-B mobility in cells. |
Single-molecule fluorescence, cryo-EM, FRAP (in cells), chromatin fiber reconstitution |
Nature communications |
High |
38086807
|
| 2024 |
DNAJC9 (a J-domain protein for H3-H4 folding) restricts CENP-A mislocalization. Its depletion promotes CENP-A interaction with MCM2, which drives CENP-A deposition at ectopic sites. H3.3 depletion also causes CENP-A mislocalization. This defines MCM2 as a driver of ectopic CENP-A deposition when H3-H4 supply chains are disrupted. |
Genome-wide RNAi screen, global interactome analysis, MCM2 depletion epistasis, immunofluorescence |
The EMBO journal |
Medium |
38600242
|
| 2016 |
Diaphanous formin mDia2 is required for stable replenishment of new CENP-A at centromeres in G1. Depletion of mDia2 causes prolonged centromere association of HJURP. mDia2 acts downstream of the MgcRacGAP-dependent small GTPase pathway in regulating CENP-A nucleosome assembly. Nuclear localization of mDia2 is required for this function. |
Quantitative imaging, pulse-chase, constitutively active mutant rescue, RNAi epistasis |
The Journal of cell biology |
Medium |
27185834
|
| 2019 |
Quiescent cells (G0-arrested and prophase I-arrested oocytes) actively and continuously incorporate new CENP-A at centromeres using the canonical CENP-A deposition machinery. Plk1 is required specifically for G1 (not quiescent) CENP-A deposition, while transcription promotes CENP-A incorporation in quiescent oocytes. Preventing CENP-A deposition during quiescence reduces CENP-A levels and perturbs chromosome segregation upon re-entry into division. |
Pulse-chase labeling, chemical inhibitors (Plk1/transcription), conditional depletion, quantitative imaging |
Developmental cell |
Medium |
31422918
|
| 2017 |
CENP-A acetylation at K124 causes tightening of the histone core and diminishes CENP-C binding (by computational modeling and CENP-A K124Q/K124A mutants). CENP-A K124 switches from acetylation at G1/S to monomethylation during early/mid-S phase. The HAT p300 is implicated in K124 acetylation. K124 mutations alter centromeric replication timing and cause modest increases in mitotic errors. |
Computational modeling, in vivo phosphomutant analysis, mass spectrometry of native CENP-A, HAT inhibitor experiments |
Epigenetics & chromatin |
Medium |
28396698
|