Evidence map›Paper›PMID 29162720›Full record

ArticleThe Journal of biological chemistry2018

Direct interactions of mitotic arrest deficient 1 (MAD1) domains with each other and MAD2 conformers are required for mitotic checkpoint signaling.

Wenbin Ji, Yibo Luo, Ejaz Ahmad, Song-Tao Liu

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Wenbin JiFrom the Department of Biological Sciences, University of Toledo, Toledo, Ohio 43606.
Yibo LuoFrom the Department of Biological Sciences, University of Toledo, Toledo, Ohio 43606.
Ejaz AhmadFrom the Department of Biological Sciences, University of Toledo, Toledo, Ohio 43606.
Song-Tao LiuFrom the Department of Biological Sciences, University of Toledo, Toledo, Ohio 43606 sliu@utnet.utoledo.edu.
University of Toledo · US

Funding

TRIP13 AAA-ATPase overexpression in chromosomal instability and breast cancerR01CA169500 · NCI · UNIVERSITY OF TOLEDO · PI LIU, SONG-TAO · 2014 to 2017
$1.4M
NCI NIH HHS R01 CA169500
6 · The paper itself

Abstract

As a sensitive signaling system, the mitotic checkpoint ensures faithful chromosome segregation by delaying anaphase onset even when a single kinetochore is unattached to mitotic spindle microtubules. The key signal amplification reaction for the checkpoint is the conformational conversion of "open" mitotic arrest deficient 2 (O-MAD2) into "closed" MAD2 (C-MAD2). The reaction has been suggested to be catalyzed by an unusual catalyst, a MAD1:C-MAD2 tetramer, but how the catalysis is executed and regulated remains elusive. Here, we report that in addition to the well-characterized middle region of MAD1 containing the MAD2-interaction motif (MIM), both N- and C-terminal domains (NTD and CTD) of MAD1 also contribute to mitotic checkpoint signaling. Unlike the MIM, which stably associated only with C-MAD2, the NTD and CTD in MAD1 surprisingly bound both O

Indexed as

Cell Cycle ProteinsCell Line, TumorHumansImmunoblottingKinetochoresMad2 ProteinsMitosisNuclear ProteinsPhosphorylationSignal TransductionSpindle ApparatusCell Cycle ProteinsMAD1L1 protein, humanMad2 ProteinsNuclear Proteinscheckpoint controlkinetochoreMAD1MAD2mitosismitotic checkpointmitotic spindleMPS1 kinasesignal transduction

Identifiers

PMID29162720
PMCPMC5767855
OpenAlexW2769396075

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.