Evidence map›Paper›PMID 42239309›Full record

ArticlebioRxiv : the preprint server for biology2026

Functional Interaction of SKA and NDC80 Complexes at Kinetochores Promoting Anaphase Onset in Mitosis.

John R Daum, Natalia Romek, Gary J Gorbsky

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

John R DaumCell Cycle & Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK USA.ORCID 0000-0001-5713-3101
Natalia RomekCell Cycle & Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK USA.ORCID 0009-0003-8147-9710
Gary J GorbskyCell Cycle & Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK USA.ORCID 0000-0003-3076-4725

Funding

Understanding Cell DivisionR35GM126980 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI GARY J. GORBSKY · 2018 to 2026
$3.7M
NIGMS NIH HHS R35 GM126980
6 · The paper itself

Abstract

The kinetochore and spindle complex (SKA) and NDC80 complexes are essential kinetochore elements that ensure highly accurate chromosome segregation and successful progression through mitosis. The SKA heterodimer complex consists of SKA1, SKA2, and SKA3 subunits, and the NDC80 complex contains NDC80, NUF2, SPC24, and SPC25 subunits. Through live cell fluorescence timelapse imaging assays and expression of RNAi-resistant SKA3 constructs, we rescue SKA complex function in cells lacking endogenous SKA3. These assays reveal a critical span within SKA3's C-terminus required for successful mitotic progression. Structural protein modeling shows that this span encompasses the majority of a roughly 40 amino acid SKA3 C-terminal structural element that promotes interaction with the coiled-coil NDC80 and NUF2 subunits of the NDC80 complex. Thus, although spindle and kinetochore concentration of the SKA complex is mediated in part by the tubulin and tip-tracking capabilities provided by the SKA1 component of the SKA complex, transition from metaphase to anaphase requires the contribution of SKA3's C-terminal structural interface to mediate interaction between the SKA and NDC80 complexes.

Indexed as

KinetochoreMitosisMitotic SpindleNDC80 ComplexResearch ReportSpindle and Kinetochore Complex

Identifiers

PMID42239309
PMCPMC13228555

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.