Evidence map›Paper›PMID 26430805›Full record

ReviewBioarchitecture2015

How the SAC gets the axe: Integrating kinetochore microtubule attachments with spindle assembly checkpoint signaling.

Shivangi Agarwal, Dileep Varma

Abstract readReview
In one paragraph

Review in Bioarchitecture, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
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

2 authors.

Shivangi Agarwala Department of Cell and Molecular Biology ; Feinberg School of Medicine; Northwestern University ; Chicago , IL USA.
Dileep Varmaa Department of Cell and Molecular Biology ; Feinberg School of Medicine; Northwestern University ; Chicago , IL USA.

Funding

Role of the Ndc80 Loop Domain and Cdt1 in Kinetochore Microtubule AttachmentsR00CA178188 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VARMA, DILEEP · 2015 to 2017
$660k
NCI NIH HHS R00 CA178188NCI NIH HHS R00CA178188
6 · The paper itself

Abstract

Mitosis entails the bona fide segregation of duplicated chromosomes. This process is accomplished by the attachment of kinetochores on chromosomes to microtubules (MTs) of the mitotic spindle. Once the appropriate attachment is achieved, the spindle assembly checkpoint (SAC) that delays the premature onset of anaphase needs to be silenced for the cell to proceed to anaphase and cytokinesis. Therefore, while it is imperative to preserve the SAC when kinetochores are unattached, it is of paramount importance that SAC components are removed post kinetochore microtubule (kMT) attachment. Precise knowledge of how kMT attachments trigger the removal of SAC components from kinetochores or how the checkpoint proteins feedback in to the attachment machinery remains elusive. This review aims to describe the recent advances that provide an insight into the interplay of molecular events that coordinate and regulate the SAC activity in response to kMT attachment during cell division.

Indexed as

MitosisSignal TransductionCell Cycle CheckpointsCell Cycle ProteinsCytoskeletal ProteinsGene Expression RegulationHumansKinetochoresMicrotubule-Associated ProteinsMicrotubulesNuclear ProteinsSpindle ApparatusCell Cycle ProteinsCytoskeletal ProteinsKnl1 protein, humanMicrotubule-Associated ProteinsNDC80 protein, humanNuclear ProteinscheckpointkinetochoreKMNKnl1microtubulemitosisNdc80spindle

Identifiers

PMID26430805
PMCPMC4832446

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.