Evidence map›Paper›PMID 42148867›Full record

ArticleJournal of cell science2026

Conditional deletion of human STN1 leads to telomere dysfunction, genome instability and proliferation defects.

Jaclyn S Holbrooks, Colin A Loveless, Kennedy A Vogler, S Donte' Reed, Grayson H Duvall, Carlan V Romney, Stephanie M Ackerson, Madison B Kircher, Jason A Stewart

Abstract read
In one paragraph

Article in Journal of cell science, 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

9 authors.

Jaclyn S HolbrooksDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.
Colin A LovelessDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.
Kennedy A VoglerDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.
S Donte' ReedDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.
Grayson H DuvallDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.
Carlan V RomneyDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA.
Stephanie M AckersonDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA.
Madison B KircherDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.
Jason A StewartDepartment of Biological Sciences, Western Kentucky University, Bowling Green, KY, 42101, USA.ORCID 0000-0003-4969-5440

Funding

WKU Lead Faculty AwardP20GM103436 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ERIC C ROUCHKA · 2012 to 2026
$60.1M
Mechanisms of Telomere Maintenance and ProtectionR15GM160955 · NIGMS · WESTERN KENTUCKY UNIVERSITY · PI STEWART, JASON AARON · 2025 to 2025
$532k
NIGMS NIH HHS P20 GM103436NIGMS NIH HHS P20GM103436NIGMS NIH HHS R15 GM160955NIGMS NIH HHS R15GM160955Western Kentucky University
6 · The paper itself

Abstract

CTC1-STN1-TEN1 (CST) is a heterotrimeric, RPA-like complex that binds single-stranded DNA, stimulates DNA polymerase α-primase, and functions in several genome maintenance pathways, including telomere maintenance and DNA replication and repair. During telomere replication, CST prevents telomerase from overextending the G-rich single-stranded DNA overhang (G-overhang) and promotes fill-in of the C-rich strand by stimulating DNA polymerase α-primase. Previous work characterized the effects of CST loss by deleting CTC1 or TEN1. Interestingly, CTC1 knockout (KO) caused severe proliferation defects and telomeric damage signaling, whereas these phenotypes were absent following TEN1 KO. Molecular analysis revealed that, while loss of CTC1 or TEN1 leads to defective C-strand fill-in, only CTC1 KO exhibited excessive G-overhang lengthening. Here, we characterized conditional STN1 KO cells and determined that STN1 KO leads to proliferation defects, telomeric damage signaling, and genome instability in the form of anaphase bridges and micronuclei. Our findings indicate that STN1 KO closely resembles CTC1 versus TEN1 KO and leads to increased genome instability.

Indexed as

Cell ProliferationGene DeletionGenomic InstabilityTelomereTelomere-Binding ProteinsDNA DamageDNA ReplicationHumansTelomere HomeostasisCtc1 protein, humanStn1 protein, humanTelomere-Binding ProteinsTen1 protein, humanCSTGenome instabilitySTN1Telomere

Identifiers

PMID42148867
PMCPMC13282564

What OpenQuestion holds

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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.