Evidence map›Paper›PMID 33988677›Full record

ArticleThe Journal of cell biology2021

Chromosome oscillation promotes Aurora A-dependent Hec1 phosphorylation and mitotic fidelity.

Kenji Iemura, Toyoaki Natsume, Kayoko Maehara, Masato T Kanemaki, Kozo Tanaka

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

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  8. Microtubule poleward flux as a target for modifying chromosome segregation errors.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  13. Targeting the deubiquitinaseOncology reports · 2023
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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

5 authors at 3 institutions in 1 country.

Kenji IemuraDepartment of Molecular Oncology, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Miyagi, Japan.ORCID 0000-0003-0829-5299
Toyoaki NatsumeDepartment of Chromosome Science, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Shizuoka, Japan.ORCID 0000-0002-3544-4491
Kayoko MaeharaDepartment of Nutrition, Graduate School of Health Sciences, Kio University, Kitakatsuragi, Nara, Japan.ORCID 0000-0001-5573-7673
Masato T KanemakiDepartment of Chromosome Science, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Shizuoka, Japan.ORCID 0000-0002-7657-1649
Kozo TanakaDepartment of Molecular Oncology, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Miyagi, Japan.ORCID 0000-0001-6086-2858
National Institute of Genetics · JPTohoku University · JPKio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most cancer cells show chromosomal instability, a condition where chromosome missegregation occurs frequently. We found that chromosome oscillation, an iterative chromosome motion during metaphase, is attenuated in cancer cell lines. We also found that metaphase phosphorylation of Hec1 at serine 55, which is mainly dependent on Aurora A on the spindle, is reduced in cancer cell lines. The Aurora A-dependent Hec1-S55 phosphorylation level was regulated by the chromosome oscillation amplitude and vice versa: Hec1-S55 and -S69 phosphorylation by Aurora A is required for efficient chromosome oscillation. Furthermore, enhancement of chromosome oscillation reduced the number of erroneous kinetochore-microtubule attachments and chromosome missegregation, whereas inhibition of Aurora A during metaphase increased such errors. We propose that Aurora A-mediated metaphase Hec1-S55 phosphorylation through chromosome oscillation, together with Hec1-S69 phosphorylation, ensures mitotic fidelity by eliminating erroneous kinetochore-microtubule attachments. Attenuated chromosome oscillation and the resulting reduced Hec1-S55 phosphorylation may be a cause of CIN in cancer cell lines.

Indexed as

Aurora Kinase AChromosomesChromosome SegregationCytoskeletal ProteinsHeLa CellsHumansKinetochoresMicrotubulesMitosisPhosphorylationSpindle ApparatusAURKA protein, humanAurora Kinase ACytoskeletal ProteinsNDC80 protein, human

Identifiers

PMID33988677
PMCPMC8129796
OpenAlexW3162465942

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.