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Removal of Spindly from microtubule-attached kinetochores controls spindle checkpoint silencing in human cells

https://doi.org/10.1101/gad.1886810
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What this work says

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

inferredcites →https://doi.org/10.1007/s00412-007-0135-3openalex-snapshot
Multiple mechanisms of chromosome movement in vertebrate cells mediated through the Ndc80 complex and dynein/dynactin
inferredcites →https://doi.org/10.1016/0092-8674(81)90014-3openalex-snapshot
S. cerevisiae genes required for cell cycle arrest in response to loss of microtubule function
inferredcites →https://doi.org/10.1016/0092-8674(81)90015-5openalex-snapshot
Feedback control of mitosis in budding yeast
inferredcites →https://doi.org/10.1016/j.cell.2006.09.047openalex-snapshot
Kinetochore Microtubule Dynamics and Attachment Stability Are Regulated by Hec1
inferredcites →https://doi.org/10.1016/j.cell.2007.08.048openalex-snapshot
p31comet Blocks Mad2 Activation through Structural Mimicry
inferredcites →https://doi.org/10.1016/j.cell.2009.03.035openalex-snapshot
Protein Architecture of the Human Kinetochore Microtubule Attachment Site
inferredcites →https://doi.org/10.1016/j.cub.2004.05.046openalex-snapshot
Dynamics of Centromere and Kinetochore Proteins
inferredcites →https://doi.org/10.1016/j.cub.2004.05.053openalex-snapshot
Spindle Checkpoint Protein Dynamics at Kinetochores in Living Cells
inferredcites →https://doi.org/10.1016/j.cub.2005.01.038openalex-snapshot
The Mad1/Mad2 Complex as a Template for Mad2 Activation in the Spindle Assembly Checkpoint
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.2007.04.056openalex-snapshot
Kinetochore Dynein Is Required for Chromosome Motion and Congression Independent of the Spindle Checkpoint
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.2009.05.060openalex-snapshot
A Novel Protein Phosphatase 1-Dependent Spindle Checkpoint Silencing Mechanism
inferredcites →https://doi.org/10.1016/j.cub.2009.06.043openalex-snapshot
Protein Phosphatase 1 Regulates Exit from the Spindle Checkpoint in Budding Yeast
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.2008.03.015openalex-snapshot
Linking Kinetochore-Microtubule Binding to the Spindle Checkpoint
inferredcites →https://doi.org/10.1016/j.sbi.2007.08.011openalex-snapshot
MAD contortions: conformational dimerization boosts spindle checkpoint signaling
inferredcites →https://doi.org/10.1016/j.str.2008.10.002openalex-snapshot
Protein Metamorphosis: The Two-State Behavior of Mad2
inferredcites →https://doi.org/10.1016/s0092-8674(01)00410-xopenalex-snapshot
Mps1 Is a Kinetochore-Associated Kinase Essential for the Vertebrate Mitotic Checkpoint
inferredcites →https://doi.org/10.1038/10049openalex-snapshot
Temporal and spatial control of cyclin B1 destruction in metaphase
inferredcites →https://doi.org/10.1038/345263a0openalex-snapshot
Cytoplasmic dynein is localized to kinetochores during mitosis
inferredcites →https://doi.org/10.1038/345266a0openalex-snapshot
Localization of cytoplasmic dynein to mitotic spindles and kinetochores
inferredcites →https://doi.org/10.1038/emboj.2009.173openalex-snapshot
The life and miracles of kinetochores
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/emboj.2009.62openalex-snapshot
Mimicking Ndc80 phosphorylation triggers spindle assembly checkpoint signalling
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/ncb1799openalex-snapshot
The APC/C maintains the spindle assembly checkpoint by targeting Cdc20 for destruction
inferredcites →https://doi.org/10.1038/nrm2163openalex-snapshot
The spindle-assembly checkpoint in space and time
inferredcites →https://doi.org/10.1038/nrm2310openalex-snapshot
Molecular architecture of the kinetochore–microtubule interface
inferredcites →https://doi.org/10.1038/nsmb748openalex-snapshot
The Mad2 spindle checkpoint protein has two distinct natively folded states
inferredcites →https://doi.org/10.1038/sj.emboj.7600135openalex-snapshot
Implication of ZW10 in membrane trafficking between the endoplasmic reticulum and Golgi
inferredcites →https://doi.org/10.1083/jcb.110.1.81openalex-snapshot
Kinetochores are transported poleward along a single astral microtubule during chromosome attachment to the spindle in newt lung cells.
inferredcites →https://doi.org/10.1083/jcb.118.4.759openalex-snapshot
The Drosophila l(1)zw10 gene product, required for accurate mitotic chromosome segregation, is redistributed at anaphase onset.
inferredcites →https://doi.org/10.1083/jcb.130.3.687openalex-snapshot
Spindle dynamics and cell cycle regulation of dynein in the budding yeast, Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1083/jcb.130.4.941openalex-snapshot
The checkpoint delaying anaphase in response to chromosome monoorientation is mediated by an inhibitory signal produced by unattached kinetochores.
inferredcites →https://doi.org/10.1083/jcb.138.6.1289openalex-snapshot
Conservation of the Centromere/Kinetochore Protein ZW10
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.150.6.1233openalex-snapshot
Visualization of Mad2 Dynamics at Kinetochores, along Spindle Fibers, and at Spindle Poles in Living Cells
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.200203035openalex-snapshot
The roles of Fzy/Cdc20 and Fzr/Cdh1 in regulating the destruction of cyclin B in space and time
inferredcites →https://doi.org/10.1083/jcb.200303167openalex-snapshot
Centromere-associated protein-E is essential for the mammalian mitotic checkpoint to prevent aneuploidy due to single chromosome loss
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.200509158openalex-snapshot
The human Mis12 complex is required for kinetochore assembly and proper chromosome segregation
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.200804114openalex-snapshot
Phosphorylation regulates targeting of cytoplasmic dynein to kinetochores during mitosis
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.200808130openalex-snapshot
Intrakinetochore stretch is associated with changes in kinetochore phosphorylation and spindle assembly checkpoint activity
inferredcites →https://doi.org/10.1083/jcb.200811028openalex-snapshot
Kinetochore stretching inactivates the spindle assembly checkpoint
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/10.1091/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.e08-05-0483openalex-snapshot
Dynein Light Intermediate Chain: An Essential Subunit That Contributes to Spindle Checkpoint Inactivation
inferredcites →https://doi.org/10.1091/mbc.e08-10-1047openalex-snapshot
Systematic Analysis in Caenorhabditis elegans Reveals that the Spindle Checkpoint Is Composed of Two Largely Independent Branches
inferredcites →https://doi.org/10.1093/emboj/18.8.2184openalex-snapshot
The disappearance of cyclin B at the end of mitosis is regulated spatially in Drosophila cells
inferredcites →https://doi.org/10.1093/emboj/cdf659openalex-snapshot
Identification of a MAD2‐binding protein, CMT2, and its role in mitosis
inferredcites →https://doi.org/10.1101/gad.1126303openalex-snapshot
KNL-1 directs assembly of the microtubule-binding interface of the kinetochore in C. elegans
inferredcites →https://doi.org/10.1101/gad.1234104openalex-snapshot
A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension
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.1882109openalex-snapshot
Overcoming inhibition in the spindle checkpoint: Figure 1.
inferredcites →https://doi.org/10.1111/j.1600-0854.2007.00646.xopenalex-snapshot
Dyneins Across Eukaryotes: A Comparative Genomic Analysis
inferredcites →https://doi.org/10.1126/science.275.5300.632openalex-snapshot
How Cells Get the Right Chromosomes
inferredcites →https://doi.org/10.1126/science.279.5353.1041openalex-snapshot
Budding Yeast Cdc20: A Target of the Spindle Checkpoint
inferredcites →https://doi.org/10.1242/jcs.01556openalex-snapshot
TruncatingAPCmutations have dominant effects on proliferation, spindle checkpoint control, survival and chromosome stability
inferredcites →https://doi.org/10.1242/jcs.114.17.3103openalex-snapshot
The ZW10 and Rough Deal checkpoint proteins function together in a large, evolutionarily conserved complex targeted to the kinetochore

What points at this work

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

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The RZZ Complex Facilitates Mad1 Binding to Bub1 Ensuring Efficient Checkpoint Signaling
inferred← citeshttps://doi.org/10.1002/cam4.70597openalex-snapshot
RIOK1 : A Novel Oncogenic Driver in Hepatocellular Carcinoma
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Molecular Mechanisms of Spindle Assembly Checkpoint Activation and Silencing
inferred← citeshttps://doi.org/10.1007/978-3-642-19065-0_4openalex-snapshot
The Spindle Assembly Checkpoint: Clock or Domino?
inferred← citeshttps://doi.org/10.1007/978-981-13-3065-0_2openalex-snapshot
Multiple Roles, Multiple Adaptors: Dynein During Cell Cycle
inferred← citeshttps://doi.org/10.1007/s00018-020-03472-4openalex-snapshot
Dynamics of kinetochore structure and its regulations during mitotic progression
inferred← citeshttps://doi.org/10.1007/s00412-012-0378-5openalex-snapshot
Connecting up and clearing out: how kinetochore attachment silences the spindle assembly checkpoint
inferred← citeshttps://doi.org/10.1007/s00412-013-0401-5openalex-snapshot
Making an effective switch at the kinetochore by phosphorylation and dephosphorylation
inferred← citeshttps://doi.org/10.1007/s00412-013-0446-5openalex-snapshot
KNL1: bringing order to the kinetochore
inferred← citeshttps://doi.org/10.1007/s00412-014-0458-9openalex-snapshot
Conditional targeting of MAD1 to kinetochores is sufficient to reactivate the spindle assembly checkpoint in metaphase
inferred← citeshttps://doi.org/10.1007/s00412-014-0468-7openalex-snapshot
Function and regulation of dynein in mitotic chromosome segregation
inferred← citeshttps://doi.org/10.1007/s00412-015-0515-zopenalex-snapshot
Connecting the microtubule attachment status of each kinetochore to cell cycle arrest through the spindle assembly checkpoint
inferred← citeshttps://doi.org/10.1007/s10577-010-9180-5openalex-snapshot
The Ndc80 complex: integrating the kinetochore's many movements
inferred← citeshttps://doi.org/10.1007/s12672-026-04576-2openalex-snapshot
SPDL1 is associated with prognosis and tumor proliferation in pancreatic adenocarcinoma
inferred← citeshttps://doi.org/10.1016/b978-0-12-382004-4.10020-2openalex-snapshot
Roles of Cytoplasmic Dynein During Mitosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.20062-xopenalex-snapshot
The Mitotic Spindle
inferred← citeshttps://doi.org/10.1016/b978-0-12-800255-1.00002-8openalex-snapshot
Microtubule Plus-End Tracking Proteins and Their Roles in Cell Division
inferred← citeshttps://doi.org/10.1016/b978-0-12-809471-6.00018-8openalex-snapshot
Role of cytoplasmic dynein and dynactin in mitotic checkpoint silencing
inferred← citeshttps://doi.org/10.1016/b978-0-12-809471-6.00019-xopenalex-snapshot
Cytoplasmic dynein during mitosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00178-4openalex-snapshot
The Mitotic Spindle
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2016.08.004openalex-snapshot
Molecular Regulation of the Spindle Assembly Checkpoint by Kinases and Phosphatases
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.02.024openalex-snapshot
Suppression of spindly delays mitotic exit and exacerbates cell death response of cancer cells treated with low doses of paclitaxel
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.10.005openalex-snapshot
Mitosis inhibitors in anticancer therapy: When blocking the exit becomes a solution
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.09.002openalex-snapshot
Mitotic Spindle Assembly and Genomic Stability in Breast Cancer Require PI3K-C2α Scaffolding Function
inferred← citeshttps://doi.org/10.1016/j.ceb.2013.12.005openalex-snapshot
Linked in: formation and regulation of microtubule attachments during chromosome segregation
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.02.016openalex-snapshot
Attachment issues: kinetochore transformations and spindle checkpoint silencing
inferred← citeshttps://doi.org/10.1016/j.cell.2019.05.035openalex-snapshot
The Cytoplasmic DNA Sensor cGAS Promotes Mitotic Cell Death
inferred← citeshttps://doi.org/10.1016/j.cell.2020.06.006openalex-snapshot
Ribosome Collisions Trigger General Stress Responses to Regulate Cell Fate
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.01.017openalex-snapshot
Interactions between N-terminal Modules in MPS1 Enable Spindle Checkpoint Silencing
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108805openalex-snapshot
The BRCT domains of ECT2 have distinct functions during cytokinesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110610openalex-snapshot
Augmin-dependent microtubule self-organization drives kinetochore fiber maturation in mammals
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117493openalex-snapshot
Single kinetochores execute an ordered series of molecular events as the spindle assembly checkpoint is silenced
inferred← citeshttps://doi.org/10.1016/j.cub.2010.05.017openalex-snapshot
Kinetochores: Orchestrating the Chromosomal Minuet
inferred← citeshttps://doi.org/10.1016/j.cub.2012.10.006openalex-snapshot
The Spindle Assembly Checkpoint
inferred← citeshttps://doi.org/10.1016/j.cub.2015.08.051openalex-snapshot
The Molecular Biology of Spindle Assembly Checkpoint Signaling Dynamics
inferred← citeshttps://doi.org/10.1016/j.cub.2018.08.056openalex-snapshot
Self-Assembly of the RZZ Complex into Filaments Drives Kinetochore Expansion in the Absence of Microtubule Attachment
inferred← citeshttps://doi.org/10.1016/j.cub.2018.10.006openalex-snapshot
Distinct Roles of RZZ and Bub1-KNL1 in Mitotic Checkpoint Signaling and Kinetochore Expansion
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.05.008openalex-snapshot
Spindle Checkpoint Silencing Requires Association of PP1 to Both Spc7 and Kinesin-8 Motors
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.06.013openalex-snapshot
Evolution and Function of the Mitotic Checkpoint
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.08.005openalex-snapshot
A Conserved RhoGAP Limits M Phase Contractility and Coordinates with Microtubule Asters to Confine RhoA during Cytokinesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.08.022openalex-snapshot
Distinct Roles of the Chromosomal Passenger Complex in the Detection of and Response to Errors in Kinetochore-Microtubule Attachment
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.09.011openalex-snapshot
Opposing motors provide mechanical and functional robustness in the human spindle
inferred← citeshttps://doi.org/10.1016/j.devcel.2023.08.012openalex-snapshot
Centrins control chicken cone cell lipid droplet dynamics through lipid-droplet-localized SPDL1
inferred← citeshttps://doi.org/10.1016/j.ejcb.2024.151430openalex-snapshot
The CCTδ subunit of the molecular chaperone CCT is required for correct localisation of p150Glued to spindle poles during mitosis
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.07.011openalex-snapshot
Dynein‐dependent transport of spindle assembly checkpoint proteins off kinetochores toward spindle poles
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.10.017openalex-snapshot
Co‐silencing of human Bub3 and dynein highlights an antagonistic relationship in regulating kinetochore–microtubule attachments
inferred← citeshttps://doi.org/10.1016/j.isci.2026.116312openalex-snapshot
hSpindly dynamics modulate spindle assembly checkpoint signaling, promoting resistance to mitotic inhibitors
inferred← citeshttps://doi.org/10.1016/j.jmb.2021.166812openalex-snapshot
The Disordered Spindly C-terminus Interacts with RZZ Subunits ROD-1 and ZWL-1 in the Kinetochore through the Same Sites in C. Elegans
inferred← citeshttps://doi.org/10.1016/j.molcel.2013.05.019openalex-snapshot
Catalytic Assembly of the Mitotic Checkpoint Inhibitor BubR1-Cdc20 by a Mad2-Induced Functional Switch in Cdc20
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.10.008openalex-snapshot
The spindle checkpoint in plants — a green variation over a conserved theme?
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.03.008openalex-snapshot
Mutual regulation between the spindle checkpoint and APC/C
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.03.008openalex-snapshot
Kinetochore assembly throughout the cell cycle
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.06.009openalex-snapshot
Spindle assembly checkpoint activation and silencing at kinetochores
inferred← citeshttps://doi.org/10.1016/j.tcb.2014.08.006openalex-snapshot
Joined at the hip: kinetochores, microtubules, and spindle assembly checkpoint signaling
inferred← citeshttps://doi.org/10.1016/j.tcb.2020.04.006openalex-snapshot
Crowning the Kinetochore: The Fibrous Corona in Chromosome Segregation
inferred← citeshttps://doi.org/10.1016/j.tibs.2013.03.004openalex-snapshot
Tracking spindle checkpoint signals from kinetochores to APC/C
inferred← citeshttps://doi.org/10.1016/j.tibs.2015.11.002openalex-snapshot
A Centromere-Signaling Network Underlies the Coordination among Mitotic Events
inferred← citeshttps://doi.org/10.1021/acs.biochem.8b01065openalex-snapshot
Incorporating Motility in the Motor: Role of the Hook Protein Family in Regulating Dynein Motility
inferred← citeshttps://doi.org/10.1021/acs.biochem.9b00772openalex-snapshot
Role of Dynactin in the Intracellular Localization and Activation of Cytoplasmic Dynein
inferred← citeshttps://doi.org/10.1038/emboj.2011.239openalex-snapshot
Probing the in vivo function of Mad1:C‐Mad2 in the spindle assembly checkpoint
inferred← citeshttps://doi.org/10.1038/emboj.2013.30openalex-snapshot
Dynactin helps target Polo‐like kinase 1 to kinetochores via its left‐handed beta‐helical p27 subunit
inferred← citeshttps://doi.org/10.1038/ncb3060openalex-snapshot
Kinetochore motors drive congression of peripheral polar chromosomes by overcoming random arm-ejection forces
inferred← citeshttps://doi.org/10.1038/ncomms10151openalex-snapshot
Cep57 is a Mis12-interacting kinetochore protein involved in kinetochore targeting of Mad1–Mad2
inferred← citeshttps://doi.org/10.1038/ncomms5795openalex-snapshot
Spatial-temporal model for silencing of the mitotic spindle assembly checkpoint
inferred← citeshttps://doi.org/10.1038/ncomms8162openalex-snapshot
Distinct domains in Bub1 localize RZZ and BubR1 to kinetochores to regulate the checkpoint
inferred← citeshttps://doi.org/10.1038/ncomms9987openalex-snapshot
Kinetochore–microtubule attachment is sufficient to satisfy the human spindle assembly checkpoint
inferred← citeshttps://doi.org/10.1038/nrm3494openalex-snapshot
Microtubule attachment and spindle assembly checkpoint signalling at the kinetochore
inferred← citeshttps://doi.org/10.1038/nrm3888openalex-snapshot
Signalling dynamics in the spindle checkpoint response
inferred← citeshttps://doi.org/10.1038/onc.2012.98openalex-snapshot
P21-activated kinase 4 (PAK4) is required for metaphase spindle positioning and anchoring
inferred← citeshttps://doi.org/10.1038/s41467-018-06774-1openalex-snapshot
TRIP13 and APC15 drive mitotic exit by turnover of interphase- and unattached kinetochore-produced MCC
inferred← citeshttps://doi.org/10.1038/s41467-023-41091-2openalex-snapshot
CENP-E activation by Aurora A and B controls kinetochore fibrous corona disassembly
inferred← citeshttps://doi.org/10.1038/s41467-024-52964-5openalex-snapshot
Kinetochore dynein is sufficient to biorient chromosomes and remodel the outer kinetochore
inferred← citeshttps://doi.org/10.1038/s41467-025-62316-6openalex-snapshot
CENcyclopedia: dynamic landscape of kinetochore architecture throughout the cell cycle
inferred← citeshttps://doi.org/10.1038/s41467-025-64148-wopenalex-snapshot
CENP-E initiates chromosome congression by opposing Aurora kinases to promote end-on attachments
inferred← citeshttps://doi.org/10.1038/s41556-018-0130-3openalex-snapshot
Dynamic kinetochore size regulation promotes microtubule capture and chromosome biorientation in mitosis
inferred← citeshttps://doi.org/10.1038/s41580-026-00988-8openalex-snapshot
Structure and function of the outer kinetochore
inferred← citeshttps://doi.org/10.1038/s41598-018-22164-5openalex-snapshot
Lateral attachment of kinetochores to microtubules is enriched in prometaphase rosette and facilitates chromosome alignment and bi-orientation establishment
inferred← citeshttps://doi.org/10.1038/s41598-018-32685-8openalex-snapshot
USP45 and Spindly are part of the same complex implicated in cell migration
inferred← citeshttps://doi.org/10.1042/bst0381645openalex-snapshot
Adapt or die: how eukaryotic cells respond to prolonged activation of the spindle assembly checkpoint
inferred← citeshttps://doi.org/10.1042/bst20140250openalex-snapshot
Sharpening the anaphase switch
inferred← citeshttps://doi.org/10.1073/pnas.1416277111openalex-snapshot
Bimodal activation of BubR1 by Bub3 sustains mitotic checkpoint signaling
inferred← citeshttps://doi.org/10.1073/pnas.2005394117openalex-snapshot
Kinetochore protein Spindly controls microtubule polarity in Drosophila axons
inferred← citeshttps://doi.org/10.1074/jbc.m111.226605openalex-snapshot
Polo-like Kinase1 Is Required for Recruitment of Dynein to Kinetochores during Mitosis
inferred← citeshttps://doi.org/10.1074/jbc.ra117.001699openalex-snapshot
Antagonism between the dynein and Ndc80 complexes at kinetochores controls the stability of kinetochore–microtubule attachments during mitosis
inferred← citeshttps://doi.org/10.1074/jbc.ra118.003154openalex-snapshot
The kinetochore proteins CENP-E and CENP-F directly and specifically interact with distinct BUB mitotic checkpoint Ser/Thr kinases
inferred← citeshttps://doi.org/10.1080/15384101.2015.1056698openalex-snapshot
Lipids beyond membranes; farnesylation targets Spindly to kinetochores
inferred← citeshttps://doi.org/10.1080/15384101.2020.1780382openalex-snapshot
RZZ-SPINDLY-DYNEIN: you got to keep ‘em separated
inferred← citeshttps://doi.org/10.1080/19490992.2015.1090669openalex-snapshot
How the SAC gets the axe: Integrating kinetochore microtubule attachments with spindle assembly checkpoint signaling
inferred← citeshttps://doi.org/10.1083/jcb.201003038openalex-snapshot
Release of Mps1 from kinetochores is crucial for timely anaphase onset
inferred← citeshttps://doi.org/10.1083/jcb.201007025openalex-snapshot
The RSC chromatin-remodeling complex influences mitotic exit and adaptation to the spindle assembly checkpoint by controlling the Cdc14 phosphatase
inferred← citeshttps://doi.org/10.1083/jcb.201008023openalex-snapshot
The astrin–kinastrin/SKAP complex localizes to microtubule plus ends and facilitates chromosome alignment
inferred← citeshttps://doi.org/10.1083/jcb.201109001openalex-snapshot
Aurora B controls kinetochore–microtubule attachments by inhibiting Ska complex–KMN network interaction
inferred← citeshttps://doi.org/10.1083/jcb.201111107openalex-snapshot
Microtubule binding by KNL-1 contributes to spindle checkpoint silencing at the kinetochore
inferred← citeshttps://doi.org/10.1083/jcb.201202112openalex-snapshot
Dynein light chain 1 and a spindle-associated adaptor promote dynein asymmetry and spindle orientation
inferred← citeshttps://doi.org/10.1083/jcb.201208098openalex-snapshot
Systematic dissection of dynein regulators in mitosis
inferred← citeshttps://doi.org/10.1083/jcb.201304197openalex-snapshot
Spindle assembly checkpoint proteins are positioned close to core microtubule attachment sites at kinetochores
inferred← citeshttps://doi.org/10.1083/jcb.201311015openalex-snapshot
A Bub1–Mad1 interaction targets the Mad1–Mad2 complex to unattached kinetochores to initiate the spindle checkpoint
inferred← citeshttps://doi.org/10.1083/jcb.201412085openalex-snapshot
A novel role of farnesylation in targeting a mitotic checkpoint protein, human Spindly, to kinetochores
inferred← citeshttps://doi.org/10.1083/jcb.201503122openalex-snapshot
RanGTP aids anaphase entry through Ubr5-mediated protein turnover
inferred← citeshttps://doi.org/10.1083/jcb.201506020openalex-snapshot
Kinetochore function is controlled by a phospho-dependent coexpansion of inner and outer components
inferred← citeshttps://doi.org/10.1083/jcb.201609061openalex-snapshot
Dual recognition of chromatin and microtubules by INCENP is important for mitotic progression
inferred← citeshttps://doi.org/10.1083/jcb.201610108openalex-snapshot
Molecular mechanism of dynein recruitment to kinetochores by the Rod–Zw10–Zwilch complex and Spindly
inferred← citeshttps://doi.org/10.1083/jcb.201611060openalex-snapshot
Structure of the RZZ complex and molecular basis of its interaction with Spindly
inferred← citeshttps://doi.org/10.1083/jcb.201611104openalex-snapshot
Spindle assembly checkpoint satisfaction occurs via end-on but not lateral attachments under tension
inferred← citeshttps://doi.org/10.1083/jcb.201902105openalex-snapshot
Mammalian kinetochores count attached microtubules in a sensitive and switch-like manner
inferred← citeshttps://doi.org/10.1083/jcb.201905018openalex-snapshot
CENP-F stabilizes kinetochore-microtubule attachments and limits dynein stripping of corona cargoes
inferred← citeshttps://doi.org/10.1083/jcb.202010179openalex-snapshot
Sequential dynein effectors regulate axonal autophagosome motility in a maturation-dependent pathway
inferred← citeshttps://doi.org/10.1083/jcb.202206131openalex-snapshot
Conformational transitions of the Spindly adaptor underlie its interaction with Dynein and Dynactin
inferred← citeshttps://doi.org/10.1083/jcb.202310022openalex-snapshot
A force-sensitive mutation reveals a non-canonical role for dynein in anaphase progression
inferred← citeshttps://doi.org/10.1091/mbc.e13-02-0076openalex-snapshot
F-actin asymmetry and the endoplasmic reticulum–associated TCC-1 protein contribute to stereotypic spindle movements in theCaenorhabditis elegansembryo
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1091/mbc.e21-09-0438openalex-snapshot
Aurora A phosphorylates Ndel1 to reduce the levels of Mad1 and NuMA at spindle poles
inferred← citeshttps://doi.org/10.1091/mbc.e23-04-0130openalex-snapshot
The role of kinetochore dynein in checkpoint silencing is restricted to disassembly of the corona
inferred← citeshttps://doi.org/10.1096/fj.202101884ropenalex-snapshot
Analysis of the potential role of fission yeast PP2A in spindle assembly checkpoint inactivation
inferred← citeshttps://doi.org/10.1098/rsob.200051openalex-snapshot
The centromere comes into focus: from CENP-A nucleosomes to kinetochore connections with the spindle
inferred← citeshttps://doi.org/10.1098/rstb.2011.0072openalex-snapshot
Spindle assembly checkpoint: the third decade
inferred← citeshttps://doi.org/10.1101/2022.03.25.485878openalex-snapshot
Lis1-dynein drives corona compaction and error-correction at kinetochores
inferred← citeshttps://doi.org/10.1101/2023.04.25.538277openalex-snapshot
A mechanism that integrates microtubule motors of opposite polarity at the kinetochore corona
inferred← citeshttps://doi.org/10.1101/2023.08.03.551815openalex-snapshot
A force-sensitive mutation reveals a spindle assembly checkpoint-independent role for dynein in anaphase progression
inferred← citeshttps://doi.org/10.1101/2023.10.19.563150openalex-snapshot
CENP-E initiates chromosome congression by opposing Aurora kinases to promote end-on attachments
inferred← citeshttps://doi.org/10.1101/2025.07.25.666731openalex-snapshot
hSpindly’s dynamic controls SAC activity independently of the KBB pathway at unattached kinetochores
inferred← citeshttps://doi.org/10.1101/276204openalex-snapshot
Kinetochore recruitment of CENP-F illustrates how paralog divergence shapes kinetochore composition and function
inferred← citeshttps://doi.org/10.1101/297580openalex-snapshot
The RZZ complex integrates spindle checkpoint maintenance with dynamic expansion of unattached kinetochores
inferred← citeshttps://doi.org/10.1111/boc.201900105openalex-snapshot
Mutations in the Drosophila rough deal gene affecting RZZ kinetochore function
inferred← citeshttps://doi.org/10.1111/cas.16406openalex-snapshot
Fibrous corona is reduced in cancer cell lines that attenuate microtubule nucleation from kinetochores
inferred← citeshttps://doi.org/10.1111/odi.13089openalex-snapshot
Spindly and Bub3 expression in oral cancer: Prognostic and therapeutic implications
inferred← citeshttps://doi.org/10.1124/mi.11.2.12openalex-snapshot
Spindle Poisons and Cell Fate: A Tale of Two Pathways
inferred← citeshttps://doi.org/10.1126/science.1246232openalex-snapshot
Crosstalk Between Microtubule Attachment Complexes Ensures Accurate Chromosome Segregation
inferred← citeshttps://doi.org/10.1126/science.aaa4029openalex-snapshot
Kinetochore attachment sensed by competitive Mps1 and microtubule binding to Ndc80C
inferred← citeshttps://doi.org/10.1126/science.aaa4055openalex-snapshot
Competition between MPS1 and microtubules at kinetochores regulates spindle checkpoint signaling
inferred← citeshttps://doi.org/10.1126/science.aat9557openalex-snapshot
A liquid-like spindle domain promotes acentrosomal spindle assembly in mammalian oocytes
inferred← citeshttps://doi.org/10.1126/science.abj3944openalex-snapshot
Mechanism of spindle pole organization and instability in human oocytes
inferred← citeshttps://doi.org/10.1126/scitranslmed.aaf7837openalex-snapshot
Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis–emphysema
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100814-125438openalex-snapshot
Mechanism and Regulation of Cytoplasmic Dynein
inferred← citeshttps://doi.org/10.1146/annurev-genet-072820-034559openalex-snapshot
The Four Causes: The Functional Architecture of Centromeres and Kinetochores
inferred← citeshttps://doi.org/10.1155/np/8895041openalex-snapshot
The Progress in Exploratory Studies of Peripheral Blood Single Nucleated Cells as Seed Cells in Peripheral Nerve Repair
inferred← citeshttps://doi.org/10.1186/s12935-022-02461-wopenalex-snapshot
Pan-cancer analysis combined with experiments explores the oncogenic role of spindle apparatus coiled-coil protein 1 (SPDL1)
inferred← citeshttps://doi.org/10.1186/s12964-026-02817-zopenalex-snapshot
Orchestrating homolog segregation in meiosis I: molecular logic and regulatory networks with emphasis on male metaphase I
inferred← citeshttps://doi.org/10.1242/bio.033233openalex-snapshot
Spindly is required for rapid migration of human cells
inferred← citeshttps://doi.org/10.1242/dev.077040openalex-snapshot
Timing of anaphase-promoting complex activation in mouse oocytes is predicted by microtubule-kinetochore attachment but not by bivalent alignment or tension
inferred← citeshttps://doi.org/10.1242/jcs.165712openalex-snapshot
A maternal effectrough dealmutation suggesting multiple pathways regulating Drosophila RZZ kinetochore recruitment
inferred← citeshttps://doi.org/10.1242/jcs.176826openalex-snapshot
A maternal effect rough deal mutation suggests that multiple pathways regulate Drosophila RZZ kinetochore recruitment
inferred← citeshttps://doi.org/10.1242/jcs.220269openalex-snapshot
Dynein at the kinetochore
inferred← citeshttps://doi.org/10.1242/jcs.227132openalex-snapshot
Dynein activators and adaptors at a glance
inferred← citeshttps://doi.org/10.1242/jcs.231589openalex-snapshot
Spindle checkpoint silencing at kinetochores with submaximal microtubule occupancy
inferred← citeshttps://doi.org/10.1242/jcs.260226openalex-snapshot
Lis1–dynein drives corona compaction and limits erroneous microtubule attachment at kinetochores
inferred← citeshttps://doi.org/10.1360/ssv-2025-0109openalex-snapshot
Research progress on dynamic assembly and regulation of centromere
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010397openalex-snapshot
Recovery from spindle checkpoint-mediated arrest requires a novel Dnt1-dependent APC/C activation mechanism
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011400openalex-snapshot
Distinct checkpoint and homolog biorientation pathways regulate meiosis I in Drosophila oocytes
inferred← citeshttps://doi.org/10.1371/journal.pone.0022969openalex-snapshot
Uncoordinated Loss of Chromatid Cohesion Is a Common Outcome of Extended Metaphase Arrest
inferred← citeshttps://doi.org/10.1371/journal.pone.0031813openalex-snapshot
Uncovering the Molecular Machinery of the Human Spindle—An Integration of Wet and Dry Systems Biology
inferred← citeshttps://doi.org/10.1371/journal.pone.0049041openalex-snapshot
Cohesion Fatigue Explains Why Pharmacological Inhibition of the APC/C Induces a Spindle Checkpoint-Dependent Mitotic Arrest
inferred← citeshttps://doi.org/10.1371/journal.pone.0164085openalex-snapshot
Dynamic ASXL1 Exon Skipping and Alternative Circular Splicing in Single Human Cells
inferred← citeshttps://doi.org/10.14348/molcells.2016.0119openalex-snapshot
N-Acetyl-D-Glucosamine Kinase Interacts with Dynein-Lis1-NudE1 Complex and Regulates Cell Division
inferred← citeshttps://doi.org/10.1515/med-2024-0922openalex-snapshot
Emerging role and function of SPDL1 in human health and diseases
inferred← citeshttps://doi.org/10.15252/embj.2018100789openalex-snapshot
Polo regulates Spindly to prevent premature stabilization of kinetochore–microtubule attachments
inferred← citeshttps://doi.org/10.15252/embj.2021110411openalex-snapshot
Structure of the RZZ complex and molecular basis of Spindly‐driven corona assembly at human kinetochores
inferred← citeshttps://doi.org/10.15252/embj.2023114838openalex-snapshot
RZZ‐Spindly and CENP‐E form an integrated platform to recruit dynein to the kinetochore corona
inferred← citeshttps://doi.org/10.15252/embr.201541143openalex-snapshot
Chromosome misalignments induce spindle‐positioning defects
inferred← citeshttps://doi.org/10.17918/etd-7146openalex-snapshot
Transcription factor specificity protein 1 (Sp1) regulates the centrochromatin landscape and centromeric transcription during mitosis
inferred← citeshttps://doi.org/10.18130/v3d57dopenalex-snapshot
The Role of Ndc80 and Ska Complexes in Maturation of Kinetochore-microtubule Attachments
inferred← citeshttps://doi.org/10.18130/v3v863openalex-snapshot
An Analysis of Spindle Microtubule Interactions Mediated by the Ndc80 Complex, Cep57R and Cep57
inferred← citeshttps://doi.org/10.18632/oncotarget.10657openalex-snapshot
Aurora B prevents premature removal of spindle assembly checkpoint proteins from the kinetochore: A key role for Aurora B in mitosis
inferred← citeshttps://doi.org/10.2174/1568009621666210129095726openalex-snapshot
The Mad2-Binding Protein p31comet as a Potential Target for Human Cancer Therapy
inferred← citeshttps://doi.org/10.3389/fcell.2014.00025openalex-snapshot
Moonlighting functions of the NRZ (mammalian Dsl1) complex
inferred← citeshttps://doi.org/10.3389/fcell.2022.787294openalex-snapshot
The Role of Mitotic Kinases and the RZZ Complex in Kinetochore-Microtubule Attachments: Doing the Right Link
inferred← citeshttps://doi.org/10.3389/fcell.2022.870745openalex-snapshot
Zombies Never Die: The Double Life Bub1 Lives in Mitosis
inferred← citeshttps://doi.org/10.3389/fcell.2022.871935openalex-snapshot
Nde1 and Ndel1: Outstanding Mysteries in Dynein-Mediated Transport
inferred← citeshttps://doi.org/10.3389/fcell.2024.1491394openalex-snapshot
Role of spindle assembly checkpoint proteins in gametogenesis and embryogenesis
inferred← citeshttps://doi.org/10.3389/fphys.2020.596263openalex-snapshot
Spindle Architectural Features Must Be Considered Along With Cell Size to Explain the Timing of Mitotic Checkpoint Silencing
inferred← citeshttps://doi.org/10.3390/biology6010005openalex-snapshot
A Molecular View of Kinetochore Assembly and Function
inferred← citeshttps://doi.org/10.3390/cells10102638openalex-snapshot
CDK1-Mediated Phosphorylation of BAG3 Promotes Mitotic Cell Shape Remodeling and the Molecular Assembly of Mitotic p62 Bodies
inferred← citeshttps://doi.org/10.3390/cells11091531openalex-snapshot
Polar Chromosomes—Challenges of a Risky Path
inferred← citeshttps://doi.org/10.3390/jdb6020009openalex-snapshot
Requirement of the Dynein-Adaptor Spindly for Mitotic and Post-Mitotic Functions in Drosophila
inferred← citeshttps://doi.org/10.3410/b2-55openalex-snapshot
Spindle checkpoint silencing: ensuring rapid and concerted anaphase onset
inferred← citeshttps://doi.org/10.3410/f.734261327.793553138openalex-snapshot
Faculty Opinions recommendation of TRIP13 and APC15 drive mitotic exit by turnover of interphase- and unattached kinetochore-produced MCC.
inferred← citeshttps://doi.org/10.34626/9d6c-c541openalex-snapshot
Functional Characterization of Dynein Cofactors in the One-Cell C. elegans Embryo
inferred← citeshttps://doi.org/10.3934/molsci.2016.4.597openalex-snapshot
The mitotic checkpoint complex (MCC): looking back and forth after 15 years
inferred← citeshttps://doi.org/10.4161/cc.29027openalex-snapshot
The current view for the silencing of the spindle assembly checkpoint
inferred← citeshttps://doi.org/10.4251/wjgo.v17.i5.104686openalex-snapshot
SPDL1 inhibition enhances colorectal cancer progression via epidermal growth factor receptor/extracellular signal-regulated kinase pathways
inferred← citeshttps://doi.org/10.53846/goediss-7653openalex-snapshot
Optimization and application of Trim-Away for studying a liquid-like spindle domain in mammalian oocytes
inferred← citeshttps://doi.org/10.64898/2026.01.26.701783openalex-snapshot
Microtubule occupancy at kinetochores links checkpoint silencing with mitotic memory
inferred← citeshttps://doi.org/10.70675/665c9010zc455z4aa8zbf42z5e9ce27230a7openalex-snapshot
Structural studies of the cytoplasmic dyneins and the BicD2 cargo adaptor
inferred← citeshttps://doi.org/10.70675/67eb2fa6z259dz4431zaa1az61680c2418edopenalex-snapshot
La protéine ATIP3 et ses partenaires d’interaction : de nouvelles cibles thérapeutiques contre le cancer du sein
inferred← citeshttps://doi.org/10.7150/jca.46173openalex-snapshot
Involvement of the NF-κB signaling pathway in proliferation and invasion inhibited by Zwint-1 deficiency in Pancreatic Cancer Cells
inferred← citeshttps://doi.org/10.7554/elife.01030openalex-snapshot
Bub3 reads phosphorylated MELT repeats to promote spindle assembly checkpoint signaling
inferred← citeshttps://doi.org/10.7554/elife.28257openalex-snapshot
The human cytoplasmic dynein interactome reveals novel activators of motility
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