Evidence map›Paper›PMID 24025336›Full record

ArticleThe Journal of biological chemistry2013

Human TEN1 maintains telomere integrity and functions in genome-wide replication restart.

Christopher Kasbek, Feng Wang, Carolyn M Price

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

62 citing papers in PubMed, 84 citations in OpenAlex.

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  20. Telomere Replication: Solving Multiple End Replication Problems.Frontiers in cell and developmental biology · 2021
    Review

2 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Christopher KasbekFrom the Department of Cancer Biology, University of Cincinnati, Cincinnati, Ohio 45267.
Feng WangFrom the Department of Cancer Biology, University of Cincinnati, Cincinnati, Ohio 45267.
Carolyn M PriceFrom the Department of Cancer Biology, University of Cincinnati, Cincinnati, Ohio 45267. Electronic address: carolyn.price@uc.edu.
University of Cincinnati · US

Funding

Training Program in Cancer TherapeuticsT32CA117846 · NCI · UNIVERSITY OF CINCINNATI · PI PRICE, CAROLYN M, TAKIAR, VINITA · 2006 to 2022
$6.5M
TELOMERE STRUCTURE IN EUPLOTES CRASSUSR01GM041803 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI PRICE, CAROLYN M · 1995 to 2017
$4.8M
A Structure/Function Analysis of CTC1 Using Coats plus/DKC MutationsF32CA177120 · NCI · UNIVERSITY OF CINCINNATI · PI KASBEK, CHRISTOPHER G · 2013 to 2014
$60k
TELOMERE STRUCTURE IN EUPLOTES CRASSUSR29GM041803 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI PRICE, CAROLYN M · 1989 to 1993
–
NCI NIH HHS F32 CA177120NCI NIH HHS F32CA177120NCI NIH HHS T32 CA117846NCI NIH HHS T32CA117846NIGMS NIH HHS GM041803NIGMS NIH HHS R01 GM041803
6 · The paper itself

Abstract

TEN1 is a component of the mammalian CTC1-STN1-TEN1 complex. CTC1 and/or STN1 functions in telomere duplex replication, C-strand fill-in, and genome-wide restart of replication following fork stalling. Here we examine the role of human TEN1 and ask whether it also functions as a specialized replication factor. TEN1 depletion causes an increase in multitelomere fluorescent in situ hybridization (FISH) signals similar to that observed after CTC1 or STN1 depletion. However, TEN1 depletion also results in increased telomere loss. This loss is not accompanied by increased telomere deprotection, recombination, or T-circle release. Thus, it appears that both the multiple telomere signals and telomere loss stem from problems in telomere duplex replication. TEN1 depletion can also affect telomere length, but whether telomeres lengthen or shorten is cell line-dependent. Like CTC1 and STN1, TEN1 is needed for G-overhang processing. Depletion of TEN1 does not effect overhang elongation in mid-S phase, but it delays overhang shortening in late S/G2. These results indicate a role for TEN1 in C-strand fill-in but do not support a direct role in telomerase regulation. Finally, TEN1 depletion causes a decrease in genome-wide replication restart following fork stalling similar to that observed after STN1 depletion. However, anaphase bridge formation is more severe than with CTC1 or STN1 depletion. Our findings indicate that TEN1 likely functions in conjunction with CTC1 and STN1 at the telomere and elsewhere in the genome. They also raise the possibility that TEN1 has additional roles and indicate that TEN1/CTC1-STN1-TEN1 helps solve a wide range of challenges to the replication machinery.

Indexed as

Cell CycleDNA ReplicationGenome, HumanHeLa CellsHumansTelomeraseTelomere-Binding ProteinsTelomere HomeostasisCtc1 protein, humanStn1 protein, humanTelomeraseTelomere-Binding ProteinsTen1 protein, humanChromosomesCSTCTC1DNA-binding ProteinDNA ReplicationGenomic InstabilityOBFC1STN1TelomeraseTelomeres

Identifiers

PMID24025336
PMCPMC3798482
OpenAlexW2014646261

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.