Evidence map›Paper›PMID 32760074›Full record

ArticlePloS one2020

A stochastic model for error correction of kinetochore-microtubule attachments in budding yeast.

Anand Banerjee, Neil Adames, Jean Peccoud, John J Tyson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Anand BanerjeeDepartment of Biological Sciences, Virginia Polytechnic Institute & State University, Blacksburg, VA, United States of America.ORCID 0000-0002-2727-3290
Neil AdamesDepartment of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO, United States of America.ORCID 0000-0003-4331-9348
Jean PeccoudDepartment of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO, United States of America.
John J TysonDepartment of Biological Sciences, Virginia Polytechnic Institute & State University, Blacksburg, VA, United States of America.
Colorado State University · USVirginia Tech · US

Funding

Stochastic Models of Cell Cycle Regulation in EukaryotesR01GM078989 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI PECCOUD, JEAN M, TYSON, JOHN J. · 2006 to 2018
$5.3M
NIGMS NIH HHS R01 GM078989
6 · The paper itself

Abstract

To divide replicated chromosomes equally between daughter cells, kinetochores must attach to microtubules emanating from opposite poles of the mitotic spindle (biorientation). An error correction mechanism facilitates this process by destabilizing erroneous kinetochore-microtubule attachments. Here we present a stochastic model of kinetochore-microtubule attachments, via an essential protein Ndc80 in budding yeast, Saccharomyces cerevisiae. Using the model, we calculate the stochastic dynamics of a pair of sister kinetochores as they transition among different attachment states. First of all, we determine the kinase-to-phosphatase balance point that maximizes the probability of biorientation, while starting from an erroneous attachment state. We find that the balance point is sensitive to the rates of microtubule-Ndc80 dissociation and derive an approximate analytical formula that defines the balance point. Secondly, we determine the probability of transition from low-tension amphitelic to monotelic attachment and find that, despite this probability being approximately 33%, biorientation can be achieved with high probability. Thirdly, we calculate the contribution of the geometrical orientation of sister kinetochores to the probability of biorientation and show that, in the absence of geometrical orientation, the biorientation error rate is much larger than that observed in experiments. Finally, we study the coupling of the error correction mechanism to the spindle assembly checkpoint by calculating the average binding of checkpoint-related proteins to the kinetochore during the error correction process.

Indexed as

Chromosome SegregationModels, GeneticKinetochoresMicrotubulesM Phase Cell Cycle CheckpointsNuclear ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsStochastic ProcessesNDC80 protein, S cerevisiaeNuclear ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID32760074
PMCPMC7410253
OpenAlexW3048049998

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.