On the public citation graph

Molecular mechanism underlying the non-essentiality of Bub1 for the fidelity of chromosome segregation in human cells

https://doi.org/10.1101/2021.02.01.429225

0 signed · 68 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1007/s10753-017-0583-8openalex-snapshot

Protective Effect of Gentianine, a compound from Du Huo Ji Sheng Tang, against Freund’s Complete Adjuvant-Induced Arthritis in Rats

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.chembiol.2008.03.013openalex-snapshot

Inhibition of Polo-like Kinase 1 by Blocking Polo-Box Domain-Dependent Protein-Protein Interactions

inferredcites →https://doi.org/10.1016/j.cub.2004.12.044openalex-snapshot

Human Bub1 Defines the Persistent Cohesion Site along the Mitotic Chromosome by Affecting Shugoshin Localization

inferredcites →https://doi.org/10.1016/j.cub.2006.12.037openalex-snapshot

BI 2536, a Potent and Selective Inhibitor of Polo-like Kinase 1, Inhibits Tumor Growth In Vivo

inferredcites →https://doi.org/10.1016/j.cub.2006.12.046openalex-snapshot

The Small-Molecule Inhibitor BI 2536 Reveals Novel Insights into Mitotic Roles of Polo-like Kinase 1

inferredcites →https://doi.org/10.1016/j.cub.2012.03.051openalex-snapshot

Phosphodependent Recruitment of Bub1 and Bub3 to Spc7/KNL1 by Mph1 Kinase Maintains the Spindle Checkpoint

inferredcites →https://doi.org/10.1016/j.cub.2012.03.052openalex-snapshot

Phosphoregulation of Spc105 by Mps1 and PP1 Regulates Bub1 Localization to Kinetochores

inferredcites →https://doi.org/10.1016/j.cub.2013.07.078openalex-snapshot

Phospho-H2A and Cohesin Specify Distinct Tension-Regulated Sgo1 Pools at Kinetochores and Inner Centromeres

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.2018.07.040openalex-snapshot

Bub1 is not essential for the checkpoint response to unattached kinetochores in diploid human cells

inferredcites →https://doi.org/10.1016/j.cub.2018.10.006openalex-snapshot

Distinct Roles of RZZ and Bub1-KNL1 in Mitotic Checkpoint Signaling and Kinetochore Expansion

inferredcites →https://doi.org/10.1016/j.cub.2019.03.051openalex-snapshot

Aurora B-INCENP Localization at Centromeres/Inner Kinetochores Is Required for Chromosome Bi-orientation in Budding Yeast

inferredcites →https://doi.org/10.1016/j.devcel.2007.08.008openalex-snapshot

Bub1 Maintains Centromeric Cohesion by Activation of the Spindle Checkpoint

inferredcites →https://doi.org/10.1016/j.devcel.2008.04.014openalex-snapshot

Polo on the Rise—from Mitotic Entry to Cytokinesis with Plk1

inferredcites →https://doi.org/10.1016/j.devcel.2017.01.012openalex-snapshot

Large-Scale Analysis of CRISPR/Cas9 Cell-Cycle Knockouts Reveals the Diversity of p53-Dependent Responses to Cell-Cycle Defects

inferredcites →https://doi.org/10.1016/j.molcel.2004.09.031openalex-snapshot

Phosphorylation of Cdc20 by Bub1 Provides a Catalytic Mechanism for APC/C Inhibition by the Spindle Checkpoint

inferredcites →https://doi.org/10.1016/j.molcel.2006.10.016openalex-snapshot

Self-Regulated Plk1 Recruitment to Kinetochores by the Plk1-PBIP1 Interaction Is Critical for Proper Chromosome Segregation

inferredcites →https://doi.org/10.1016/j.molcel.2014.12.036openalex-snapshot

Sequential Multisite Phospho-Regulation of KNL1-BUB3 Interfaces at Mitotic Kinetochores

inferredcites →https://doi.org/10.1016/j.molcel.2015.06.018openalex-snapshot

Mitotic Transcription Installs Sgo1 at Centromeres to Coordinate Chromosome Segregation

inferredcites →https://doi.org/10.1016/j.molcel.2015.10.027openalex-snapshot

The CENP-L-N Complex Forms a Critical Node in an Integrated Meshwork of Interactions at the Centromere-Kinetochore Interface

inferredcites →https://doi.org/10.1016/j.molcel.2018.03.032openalex-snapshot

The BUB3-BUB1 Complex Promotes Telomere DNA Replication

inferredcites →https://doi.org/10.1016/j.molcel.2020.10.040openalex-snapshot

BUB1 and CENP-U, Primed by CDK1, Are the Main PLK1 Kinetochore Receptors in Mitosis

inferredcites →https://doi.org/10.1016/j.tibs.2010.08.004openalex-snapshot

BUB1 and BUBR1: multifaceted kinases of the cell cycle

inferredcites →https://doi.org/10.1016/s0092-8674(00)80255-xopenalex-snapshot

Kinetochore Localization of Murine Bub1 Is Required for Normal Mitotic Timing and Checkpoint Response to Spindle Damage

inferredcites →https://doi.org/10.1016/s0092-8674(04)00171-0openalex-snapshot

From Silencing to Gene Expression

inferredcites →https://doi.org/10.1038/nature02312openalex-snapshot

The conserved kinetochore protein shugoshin protects centromeric cohesion during meiosis

inferredcites →https://doi.org/10.1038/nature09390openalex-snapshot

Phosphorylation of the CPC by Cdk1 promotes chromosome bi-orientation

inferredcites →https://doi.org/10.1038/ncb1102openalex-snapshot

Correcting improper chromosome–spindle attachments during cell division

inferredcites →https://doi.org/10.1038/ncb2515openalex-snapshot

MPS1/Mph1 phosphorylates the kinetochore protein KNL1/Spc7 to recruit SAC components

inferredcites →https://doi.org/10.1038/ncb2637openalex-snapshot

Phosphorylation-enabled binding of SGO1–PP2A to cohesin protects sororin and centromeric cohesion during mitosis

inferredcites →https://doi.org/10.1038/nchembio.2060openalex-snapshot

Decoding Polo-like kinase 1 signaling along the kinetochore–centromere axis

inferredcites →https://doi.org/10.1038/ncomms10818openalex-snapshot

The Bub1–Plk1 kinase complex promotes spindle checkpoint signalling through Cdc20 phosphorylation

inferredcites →https://doi.org/10.1038/nrc2964openalex-snapshot

Shared and separate functions of polo-like kinases and aurora kinases in cancer

inferredcites →https://doi.org/10.1038/nrd3184openalex-snapshot

Multifaceted polo-like kinases: drug targets and antitargets for cancer therapy

inferredcites →https://doi.org/10.1038/nrm3888openalex-snapshot

Signalling dynamics in the spindle checkpoint response

inferredcites →https://doi.org/10.1038/onc.2017.113openalex-snapshot

Playing polo during mitosis: PLK1 takes the lead

inferredcites →https://doi.org/10.1038/s41467-019-10938-yopenalex-snapshot

PLK1 facilitates chromosome biorientation by suppressing centromere disintegration driven by BLM-mediated unwinding and spindle pulling

inferredcites →https://doi.org/10.1073/pnas.0408600102openalex-snapshot

Human Bub1 protects centromeric sister-chromatid cohesion through Shugoshin during mitosis

inferredcites →https://doi.org/10.1074/jbc.m511735200openalex-snapshot

S-Trityl-L-cysteine Is a Reversible, Tight Binding Inhibitor of the Human Kinesin Eg5 That Specifically Blocks Mitotic Progression

inferredcites →https://doi.org/10.1074/jbc.m805308200openalex-snapshot

Deficiency in Chromosome Congression by the Inhibition of Plk1 Polo Box Domain-dependent Recognition

inferredcites →https://doi.org/10.1080/23723556.2019.1658515openalex-snapshot

Another string to the polo bow: a new mitotic role of PLK1 in centromere protection

inferredcites →https://doi.org/10.1083/jcb.200609044openalex-snapshot

Bub1 is essential for assembly of the functional inner centromere

inferredcites →https://doi.org/10.1083/jcb.201905144openalex-snapshot

Aurora B kinase is recruited to multiple discrete kinetochore and centromere regions in human cells

inferredcites →https://doi.org/10.1083/jcb.201907087openalex-snapshot

Untangling the contribution of Haspin and Bub1 to Aurora B function during mitosis

inferredcites →https://doi.org/10.1083/jcb.201907092openalex-snapshot

Centromere-localized Aurora B kinase is required for the fidelity of chromosome segregation

inferredcites →https://doi.org/10.1091/mbc.e06-03-0240openalex-snapshot

Phosphorylation- and Polo-Box–dependent Binding of Plk1 to Bub1 Is Required for the Kinetochore Localization of Plk1

inferredcites →https://doi.org/10.1091/mbc.e07-06-0556openalex-snapshot

CENP-O Class Proteins Form a Stable Complex and Are Required for Proper Kinetochore Function

inferredcites →https://doi.org/10.1101/gad.233700.113openalex-snapshot

Mad1 kinetochore recruitment by Mps1-mediated phosphorylation of Bub1 signals the spindle checkpoint

inferredcites →https://doi.org/10.1126/science.1180189openalex-snapshot

Phosphorylation of H2A by Bub1 Prevents Chromosomal Instability Through Localizing Shugoshin

inferredcites →https://doi.org/10.1126/science.1189435openalex-snapshot

Histone H3 Thr-3 Phosphorylation by Haspin Positions Aurora B at Centromeres in Mitosis

inferredcites →https://doi.org/10.1126/science.1189505openalex-snapshot

Survivin Reads Phosphorylated Histone H3 Threonine 3 to Activate the Mitotic Kinase Aurora B

inferredcites →https://doi.org/10.1126/science.1194498openalex-snapshot

Two Histone Marks Establish the Inner Centromere and Chromosome Bi-Orientation

inferredcites →https://doi.org/10.1126/science.aac7041openalex-snapshot

Identification and characterization of essential genes in the human genome

inferredcites →https://doi.org/10.1128/mcb.05326-11openalex-snapshot

Bub1 and BubR1: at the Interface between Chromosome Attachment and the Spindle Checkpoint

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.114.24.4385openalex-snapshot

Kinetochore localisation and phosphorylation of the mitotic checkpoint components Bub1 and BubR1 are differentially regulated by spindle events in human cells

inferredcites →https://doi.org/10.1371/journal.pbio.1001250openalex-snapshot

The Chromosomal Passenger Complex Activates Polo Kinase at Centromeres

inferredcites →https://doi.org/10.15252/embj.2018100977openalex-snapshot

Efficient mitotic checkpoint signaling depends on integrated activities of Bub1 and the RZZ complex

inferredcites →https://doi.org/10.15252/embj.2019101863openalex-snapshot

Histone H2A phosphorylation recruits topoisomerase IIα to centromeres to safeguard genomic stability

inferredcites →https://doi.org/10.15252/embj.2019102423openalex-snapshot

Killing a zombie: a full deletion of the BUB1 gene in HAP1 cells

inferredcites →https://doi.org/10.15252/embj.2019103547openalex-snapshot

Response to Raaijmakers & Medema

inferredcites →https://doi.org/10.15252/embr.201948711openalex-snapshot

Plk1 protects kinetochore–centromere architecture against microtubule pulling forces

inferredcites →https://doi.org/10.3389/fcell.2017.00112openalex-snapshot

The Ins and Outs of Aurora B Inner Centromere Localization

inferredcites →https://doi.org/10.3389/fcell.2018.00062openalex-snapshot

Kinase and Phosphatase Cross-Talk at the Kinetochore

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.42879openalex-snapshot

The COMA complex interacts with Cse4 and positions Sli15/Ipl1 at the budding yeast inner kinetochore

What points at this work

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

inferred← citeshttps://doi.org/10.1371/journal.pgen.1010903openalex-snapshot

Genetic enhancers of partial PLK1 inhibition reveal hypersensitivity to kinetochore perturbations

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.