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Kinetochore recruitment of CENP-F illustrates how paralog divergence shapes kinetochore composition and function
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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/cm.970260305openalex-snapshot
CENP‐F is a ca 400 kDa kinetochore protein that exhibits a cell‐cycle dependent localization
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb08066.xopenalex-snapshot
CENP‐E, a novel human centromere‐associated protein required for progression from metaphase to anaphase.
inferredcites →https://doi.org/10.1007/bf00337241openalex-snapshot
Chromosomal passengers: Toward an integrated view of mitosis
inferredcites →https://doi.org/10.1007/s00412-006-0049-5openalex-snapshot
CENP-F is a novel microtubule-binding protein that is essential for kinetochore attachments and affects the duration of the mitotic checkpoint delay
inferredcites →https://doi.org/10.1007/s004120050266openalex-snapshot
Localization of CENP-E in the fibrous corona and outer plate of mammalian kinetochores from prometaphase through anaphase
inferredcites →https://doi.org/10.1016/bs.mie.2015.05.001openalex-snapshot
Calculations and Publication-Quality Illustrations for Analytical Ultracentrifugation Data
inferredcites →https://doi.org/10.1016/j.cell.2011.07.012openalex-snapshot
The Spatial Arrangement of Chromosomes during Prometaphase Facilitates Spindle Assembly
inferredcites →https://doi.org/10.1016/j.cell.2013.08.024openalex-snapshot
Dynein Recruitment to Nuclear Pores Activates Apical Nuclear Migration and Mitotic Entry in Brain Progenitor Cells
inferredcites →https://doi.org/10.1016/j.celrep.2018.01.034openalex-snapshot
BUB1 Is Essential for the Viability of Human Cells in which the Spindle Assembly Checkpoint Is Compromised
inferredcites →https://doi.org/10.1016/j.cub.2003.12.025openalex-snapshot
In Vivo Dynamics of the Rough Deal Checkpoint Protein during Drosophila Mitosis
inferredcites →https://doi.org/10.1016/j.cub.2005.03.052openalex-snapshot
Recruitment of Mad2 to the Kinetochore Requires the Rod/Zw10 Complex
inferredcites →https://doi.org/10.1016/j.cub.2007.05.077openalex-snapshot
Cenp-F Links Kinetochores to Ndel1/Nde1/Lis1/Dynein Microtubule Motor Complexes
inferredcites →https://doi.org/10.1016/j.cub.2015.08.051openalex-snapshot
The Molecular Biology of Spindle Assembly Checkpoint Signaling Dynamics
inferredcites →https://doi.org/10.1016/j.cub.2017.08.033openalex-snapshot
BubR1 Promotes Bub3-Dependent APC/C Inhibition during Spindle Assembly Checkpoint Signaling
inferredcites →https://doi.org/10.1016/j.devcel.2007.09.005openalex-snapshot
Human Blinkin/AF15q14 Is Required for Chromosome Alignment and the Mitotic Checkpoint through Direct Interaction with Bub1 and BubR1
inferredcites →https://doi.org/10.1016/j.devcel.2012.03.009openalex-snapshot
The Vertebrate Mitotic Checkpoint Protein BUBR1 Is an Unusual Pseudokinase
inferredcites →https://doi.org/10.1016/j.devcel.2015.04.022openalex-snapshot
Cdk1 Activates Pre-mitotic Nuclear Envelope Dynein Recruitment and Apical Nuclear Migration in Neural Stem Cells
inferredcites →https://doi.org/10.1016/j.devcel.2015.11.012openalex-snapshot
KNL1-Bubs and RZZ Provide Two Separable Pathways for Checkpoint Activation at Human Kinetochores
inferredcites →https://doi.org/10.1016/j.jmb.2013.07.027openalex-snapshot
The Microtubule Binding Properties of CENP-E's C-Terminus and CENP-F
inferredcites →https://doi.org/10.1016/j.str.2010.02.014openalex-snapshot
Structural Analysis of the RZZ Complex Reveals Common Ancestry with Multisubunit Vesicle Tethering Machinery
inferredcites →https://doi.org/10.1016/s0022-5320(67)80058-3openalex-snapshot
The ultrastructure and spatial organization of the metaphase kinetochore in mitotic rat cells
inferredcites →https://doi.org/10.1016/s0074-7696(08)61672-1openalex-snapshot
The Formation, Structure, and Composition of the Mammalian Kinetochore and Kinetochore Fiber
inferredcites →https://doi.org/10.1016/s0092-8674(00)80419-5openalex-snapshot
CENP-E Is a Plus End–Directed Kinetochore Motor Required for Metaphase Chromosome Alignment
inferredcites →https://doi.org/10.1016/s0092-8674(03)00475-6openalex-snapshot
Activating and Silencing the Mitotic Checkpoint through CENP-E-Dependent Activation/Inactivation of BubR1
inferredcites →https://doi.org/10.1016/s1534-5807(02)00255-1openalex-snapshot
Unstable Kinetochore-Microtubule Capture and Chromosomal Instability Following Deletion of CENP-E
inferredcites →https://doi.org/10.1038/35019518openalex-snapshot
CENP-E forms a link between attachment of spindle microtubules to kinetochores and the mitotic checkpoint
inferredcites →https://doi.org/10.1038/35046592openalex-snapshot
Rough Deal and Zw10 are required for the metaphase checkpoint in Drosophila
inferredcites →https://doi.org/10.1038/359536a0openalex-snapshot
CENP-E is a putative kinetochore motor that accumulates just before mitosis
inferredcites →https://doi.org/10.1038/emboj.2009.38openalex-snapshot
Dynein light intermediate chain 1 is required for progress through the spindle assembly checkpoint
inferredcites →https://doi.org/10.1038/ncb1101-1001openalex-snapshot
Kinetochore dynein: its dynamics and role in the transport of the Rough deal checkpoint protein
inferredcites →https://doi.org/10.1038/ncb1208openalex-snapshot
The human mitotic checkpoint protein BubR1 regulates chromosome–spindle attachments
inferredcites →https://doi.org/10.1038/ncb3219openalex-snapshot
Mad1 promotes chromosome congression by anchoring a kinesin motor to the kinetochore
inferredcites →https://doi.org/10.1038/ncb3223openalex-snapshot
Adaptive changes in the kinetochore architecture facilitate proper spindle assembly
inferredcites →https://doi.org/10.1038/ncomms8162openalex-snapshot
Distinct domains in Bub1 localize RZZ and BubR1 to kinetochores to regulate the checkpoint
inferredcites →https://doi.org/10.1038/nrm2310openalex-snapshot
Molecular architecture of the kinetochore–microtubule interface
inferredcites →https://doi.org/10.1038/nrm4001openalex-snapshot
Discovering centromere proteins: from cold white hands to the A, B, C of CENPs
inferredcites →https://doi.org/10.1038/sj.emboj.7600848openalex-snapshot
Unstable microtubule capture at kinetochores depleted of the centromere‐associated protein CENP‐F
inferredcites →https://doi.org/10.1073/pnas.1604935113openalex-snapshot
biGBac enables rapid gene assembly for the expression of large multisubunit protein complexes
inferredcites →https://doi.org/10.1074/jbc.270.33.19545openalex-snapshot
The C Terminus of Mitosin Is Essential for Its Nuclear Localization, Centromere/Kinetochore Targeting, and Dimerization
inferredcites →https://doi.org/10.1074/jbc.m003469200openalex-snapshot
Farnesyl Transferase Inhibitors Block the Farnesylation of CENP-E and CENP-F and Alter the Association of CENP-E with the Microtubules
inferredcites →https://doi.org/10.1083/jcb.120.2.301openalex-snapshot
Structure of the colcemid-treated PtK1 kinetochore outer plate as determined by high voltage electron microscopic tomography.
inferredcites →https://doi.org/10.1083/jcb.130.3.507openalex-snapshot
CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis.
inferredcites →https://doi.org/10.1083/jcb.134.5.1127openalex-snapshot
Bipolar spindle attachments affect redistributions of ZW10, a Drosophila centromere/kinetochore component required for accurate chromosome segregation.
inferredcites →https://doi.org/10.1083/jcb.139.2.435openalex-snapshot
The Microtubule-dependent Motor Centromere–associated Protein E (CENP-E) Is an Integral Component of Kinetochore Corona Fibers That Link Centromeres to Spindle Microtubules
inferredcites →https://doi.org/10.1083/jcb.139.6.1373openalex-snapshot
CENP-E Function at Kinetochores Is Essential for Chromosome Alignment
inferredcites →https://doi.org/10.1083/jcb.142.3.763openalex-snapshot
ZW10 Helps Recruit Dynactin and Dynein to the Kinetochore
inferredcites →https://doi.org/10.1083/jcb.143.1.49openalex-snapshot
Characterization of the Kinetochore Binding Domain of CENP-E Reveals Interactions with the Kinetochore Proteins CENP-F and hBUBR1
inferredcites →https://doi.org/10.1083/jcb.153.6.1239openalex-snapshot
Spindle Checkpoint Protein Bub1 Is Required for Kinetochore Localization of Mad1, Mad2, Bub3, and Cenp-E, Independently of Its Kinase Activity
inferredcites →https://doi.org/10.1083/jcb.200102093openalex-snapshot
Checkpoint inhibition of the APC/C in HeLa cells is mediated by a complex of BUBR1, BUB3, CDC20, and MAD2
inferredcites →https://doi.org/10.1083/jcb.200105093openalex-snapshot
Cytoplasmic dynein/dynactin drives kinetochore protein transport to the spindle poles and has a role in mitotic spindle checkpoint inactivation
inferredcites →https://doi.org/10.1083/jcb.200411118openalex-snapshot
ZW10 links mitotic checkpoint signaling to the structural kinetochore
inferredcites →https://doi.org/10.1083/jcb.200505040openalex-snapshot
Microtubule capture by CENP-E silences BubR1-dependent mitotic checkpoint signaling
inferredcites →https://doi.org/10.1083/jcb.200606020openalex-snapshot
Mapping the assembly pathways that specify formation of the trilaminar kinetochore plates in human cells
inferredcites →https://doi.org/10.1083/jcb.200702062openalex-snapshot
Spindly, a novel protein essential for silencing the spindle assembly checkpoint, recruits dynein to the kinetochore
inferredcites →https://doi.org/10.1083/jcb.200710106openalex-snapshot
Direct role of dynein motor in stable kinetochore-microtubule attachment, orientation, and alignment
inferredcites →https://doi.org/10.1083/jcb.200802189openalex-snapshot
CENP-E combines a slow, processive motor and a flexible coiled coil to produce an essential motile kinetochore tether
inferredcites →https://doi.org/10.1083/jcb.200805185openalex-snapshot
SPDL-1 functions as a kinetochore receptor for MDF-1 in Caenorhabditis elegans
inferredcites →https://doi.org/10.1083/jcb.200812167openalex-snapshot
Mitotic control of kinetochore-associated dynein and spindle orientation by human Spindly
inferredcites →https://doi.org/10.1083/jcb.200902128openalex-snapshot
Bub1 regulates chromosome segregation in a kinetochore-independent manner
inferredcites →https://doi.org/10.1083/jcb.201007118openalex-snapshot
A Nup133-dependent NPC-anchored network tethers centrosomes to the nuclear envelope in prophase
inferredcites →https://doi.org/10.1083/jcb.201110013openalex-snapshot
Structural analysis reveals features of the spindle checkpoint kinase Bub1–kinetochore subunit Knl1 interaction
inferredcites →https://doi.org/10.1083/jcb.201307137openalex-snapshot
CENP-I and Aurora B act as a molecular switch that ties RZZ/Mad1 recruitment to kinetochore attachment status
inferredcites →https://doi.org/10.1083/jcb.201408083openalex-snapshot
Centromere protein F includes two sites that couple efficiently to depolymerizing microtubules
inferredcites →https://doi.org/10.1083/jcb.201412085openalex-snapshot
A novel role of farnesylation in targeting a mitotic checkpoint protein, human Spindly, to kinetochores
inferredcites →https://doi.org/10.1083/jcb.201506020openalex-snapshot
Kinetochore function is controlled by a phospho-dependent coexpansion of inner and outer components
inferredcites →https://doi.org/10.1083/jcb.201610108openalex-snapshot
Molecular mechanism of dynein recruitment to kinetochores by the Rod–Zw10–Zwilch complex and Spindly
inferredcites →https://doi.org/10.1083/jcb.201611060openalex-snapshot
Structure of the RZZ complex and molecular basis of its interaction with Spindly
inferredcites →https://doi.org/10.1083/jcb.201611104openalex-snapshot
Spindle assembly checkpoint satisfaction occurs via end-on but not lateral attachments under tension
inferredcites →https://doi.org/10.1091/mbc.12.7.1995openalex-snapshot
Microtubule-dependent Changes in Assembly of Microtubule Motor Proteins and Mitotic Spindle Checkpoint Proteins at PtK1 Kinetochores
inferredcites →https://doi.org/10.1091/mbc.e07-07-0633openalex-snapshot
The Human Spindle Assembly Checkpoint Protein Bub3 Is Required for the Establishment of Efficient Kinetochore–Microtubule Attachments
inferredcites →https://doi.org/10.1091/mbc.e08-05-0483openalex-snapshot
Dynein Light Intermediate Chain: An Essential Subunit That Contributes to Spindle Checkpoint Inactivation
inferredcites →https://doi.org/10.1091/mbc.e09-04-0356openalex-snapshot
Spindly/CCDC99 Is Required for Efficient Chromosome Congression and Mitotic Checkpoint Regulation
inferredcites →https://doi.org/10.1091/mbc.e14-11-1560openalex-snapshot
Preventing farnesylation of the dynein adaptor Spindly contributes to the mitotic defects caused by farnesyltransferase inhibitors
inferredcites →https://doi.org/10.1093/bioinformatics/18.4.617openalex-snapshot
An HMM model for coiled-coil domains and a comparison with PSSM-based predictions
inferredcites →https://doi.org/10.1093/nar/28.16.e78openalex-snapshot
Directed evolution of green fluorescent protein by a new versatile PCR strategy for site-directed and semi-random mutagenesis
inferredcites →https://doi.org/10.1093/nar/gki405openalex-snapshot
REPPER--repeats and their periodicities in fibrous proteins
inferredcites →https://doi.org/10.1098/rsob.150160openalex-snapshot
The RZZ complex requires the N-terminus of KNL1 to mediate optimal Mad1 kinetochore localization in human cells
inferredcites →https://doi.org/10.1101/gad.1687508openalex-snapshot
A new mechanism controlling kinetochore–microtubule interactions revealed by comparison of two dynein-targeting components: SPDL-1 and the Rod/Zwilch/Zw10 complex
inferredcites →https://doi.org/10.1101/gad.1886810openalex-snapshot
Removal of Spindly from microtubule-attached kinetochores controls spindle checkpoint silencing in human cells
inferredcites →https://doi.org/10.1126/science.1075596openalex-snapshot
Role of Hec1 in Spindle Checkpoint Signaling and Kinetochore Recruitment of Mad1/Mad2
inferredcites →https://doi.org/10.1126/science.1122142openalex-snapshot
Chromosomes Can Congress to the Metaphase Plate Before Biorientation
inferredcites →https://doi.org/10.1126/science.1246232openalex-snapshot
Crosstalk Between Microtubule Attachment Complexes Ensures Accurate Chromosome Segregation
inferredcites →https://doi.org/10.1126/science.252.5009.1162openalex-snapshot
Predicting Coiled Coils from Protein Sequences
inferredcites →https://doi.org/10.1126/science.8023161openalex-snapshot
Mitotic Regulation of Microtubule Cross-Linking Activity of CENP-E Kinetochore Protein
inferredcites →https://doi.org/10.1128/mcb.15.9.5017openalex-snapshot
Characterization of a Novel 350-Kilodalton Nuclear Phosphoprotein That Is Specifically Involved in Mitotic-Phase Progression
inferredcites →https://doi.org/10.1128/mcb.19.2.1016openalex-snapshot
Structural Requirements and Dynamics of Mitosin-Kinetochore Interaction in M Phase
inferredcites →https://doi.org/10.1128/mcb.25.10.4062-4074.2005openalex-snapshot
Silencing Mitosin Induces Misaligned Chromosomes, Premature Chromosome Decondensation before Anaphase Onset, and Mitotic Cell Death
inferredcites →https://doi.org/10.1158/1535-7163.mct-06-0703openalex-snapshot
Farnesyl transferase inhibitors impair chromosomal maintenance in cell lines and human tumors by compromising CENP-E and CENP-F function
inferredcites →https://doi.org/10.1242/jcs.01006openalex-snapshot
Bub1 is required for kinetochore localization of BubR1, Cenp-E, Cenp-F and Mad2, and chromosome congression
inferredcites →https://doi.org/10.1242/jcs.02614openalex-snapshot
Silencing Cenp-F weakens centromeric cohesion, prevents chromosome alignment and activates the spindle checkpoint
inferredcites →https://doi.org/10.1242/jcs.106.4.1045openalex-snapshot
Autoantibodies to a novel cell cycle-regulated protein that accumulates in the nuclear matrix during S phase and is localized in the kinetochores and spindle midzone during mitosis
inferredcites →https://doi.org/10.1242/jcs.115.17.3403openalex-snapshot
Farnesylation of Cenp-F is required for G2/M progression and degradation after mitosis
inferredcites →https://doi.org/10.1242/jcs.212159openalex-snapshot
NudE regulates dynein at kinetochores but is dispensable for other dynein functions in the C. elegans early embryo
inferredcites →https://doi.org/10.1371/journal.pone.0144673openalex-snapshot
Role of Intrinsic and Extrinsic Factors in the Regulation of the Mitotic Checkpoint Kinase Bub1
inferredcites →https://doi.org/10.15252/embr.201744102openalex-snapshot
Evolutionary dynamics of the kinetochore network in eukaryotes as revealed by comparative genomics
inferredcites →https://doi.org/10.15252/embr.201744742openalex-snapshot
Disentangling the molecular determinants for Cenp‐F localization to nuclear pores and kinetochores
inferredcites →https://doi.org/10.1529/biophysj.106.081372openalex-snapshot
Macromolecular Size-and-Shape Distributions by Sedimentation Velocity Analytical Ultracentrifugation
inferredcites →https://doi.org/10.3390/biology6010005openalex-snapshot
A Molecular View of Kinetochore Assembly and Function
inferredcites →https://doi.org/10.7554/elife.01030openalex-snapshot
Bub3 reads phosphorylated MELT repeats to promote spindle assembly checkpoint signaling
inferredcites →https://doi.org/10.7554/elife.05269openalex-snapshot
A molecular basis for the differential roles of Bub1 and BubR1 in the spindle assembly checkpoint
inferredcites →https://doi.org/10.7554/elife.21007openalex-snapshot
Molecular basis of outer kinetochore assembly on CENP-T
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.15252/embr.201744742openalex-snapshot
Disentangling the molecular determinants for Cenp‐F localization to nuclear pores and kinetochores
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