Evidence map›Paper›PMID 24187132›Full record

ArticleThe Journal of biological chemistry2013

Phosphorylation of microtubule-binding protein Hec1 by mitotic kinase Aurora B specifies spindle checkpoint kinase Mps1 signaling at the kinetochore.

Tongge Zhu, Zhen Dou, Bo Qin, Changjiang Jin, Xinghui Wang, Leilei Xu, Zhaoyang Wang, Lijuan Zhu, Fusheng Liu, Xinjiao Gao and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 67 citations in OpenAlex.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

Tongge ZhuFrom the Anhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science and Technology of China, Hefei 230026, China.
Zhen Dou
Bo Qin
Changjiang Jin
Xinghui Wang
Leilei Xu
Zhaoyang Wang
Lijuan Zhu
Fusheng Liu
Xinjiao Gao
Yuwen Ke
Zhiyong Wang
Felix Aikhionbare
Chuanhai Fu
Xia Ding
Xuebiao Yao
University of Science and Technology of China · CNImaging Center · USMorehouse School of Medicine · USBeijing University of Chinese Medicine · CN

Funding

Morehouse School of Medicine Center of Excellence Research Endowment ProgramS21MD000101 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI MONTGOMERY-RICE, VALERIE C. · 2001 to 2015
$74.3M
TRANSCRIPTION FACTORS AND PROSTATE CANCERG12RR003034 · NCRR · MOREHOUSE SCHOOL OF MEDICINE · PI ZHAO, XUEYING · 1986 to 2011
$32.4M
TRANSPLANTATION OF EXOSOMES FROM HYPOXIA-PRECONDITIONED ADIPOSE-DERIVED STEM CELLS PROMOTES ANGIOGENESIS IN ISCHEMIC HEARTG12MD007602 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI BOND, VINCENT C · 2012 to 2017
$18.4M
The function of ezrin in stimulus-coupled acid secretionR01DK056292 · NIDDK · UNIVERSITY OF WISCONSIN MADISON · PI YAO, XUEBIAO · 1999 to 2012
$2.5M
Function of ACAP4 in CCL18-stimulated breast cancer metastasisR01CA164133 · NCI · MOREHOUSE SCHOOL OF MEDICINE · PI YAO, XUEBIAO · 2012 to 2016
$1.4M
NCI NIH HHS CA164133NCI NIH HHS R01 CA164133NCRR NIH HHS G12 RR003034NCRR NIH HHS G12RR03034NIDDK NIH HHS DK56292NIDDK NIH HHS R01 DK056292NIMHD NIH HHS 8G12MD007602NIMHD NIH HHS G12 MD007602NIMHD NIH HHS S21 MD000101
6 · The paper itself

Abstract

The spindle assembly checkpoint (SAC) is a quality control device to ensure accurate chromosome attachment to spindle microtubule for equal segregation of sister chromatid. Aurora B is essential for SAC function by sensing chromosome bi-orientation via spatial regulation of kinetochore substrates. However, it has remained elusive as to how Aurora B couples kinetochore-microtubule attachment to SAC signaling. Here, we show that Hec1 interacts with Mps1 and specifies its kinetochore localization via its calponin homology (CH) domain and N-terminal 80 amino acids. Interestingly, phosphorylation of the Hec1 by Aurora B weakens its interaction with microtubules but promotes Hec1 binding to Mps1. Significantly, the temporal regulation of Hec1 phosphorylation orchestrates kinetochore-microtubule attachment and Mps1 loading to the kinetochore. Persistent expression of phosphomimetic Hec1 mutant induces a hyperactivation of SAC, suggesting that phosphorylation-elicited Hec1 conformational change is used as a switch to orchestrate SAC activation to concurrent destabilization of aberrant kinetochore attachment. Taken together, these results define a novel role for Aurora B-Hec1-Mps1 signaling axis in governing accurate chromosome segregation in mitosis.

Indexed as

M Phase Cell Cycle CheckpointsSignal TransductionAurora Kinase BCell Cycle CheckpointsCell Cycle ProteinsCytoskeletal ProteinsGene Expression RegulationHeLa CellsHumansKinetochoresMicrotubulesNuclear ProteinsPhosphorylationProtein Serine-Threonine KinasesProtein Structure, TertiaryProtein TransportAURKB protein, humanAurora Kinase BCell Cycle ProteinsCytoskeletal ProteinsNDC80 protein, humanNuclear ProteinsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesTTK protein, humanCenp-eCheckpointCheckpoint ControlKinetochoreMitosisMitotic SpindlePhosphorylation

Identifiers

PMID24187132
PMCPMC3861662
OpenAlexW2145459347

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.