Evidence map›Paper›PMID 32499435›Full record

ArticleScience (New York, N.Y.)2020

The structure of human CST reveals a decameric assembly bound to telomeric DNA.

Ci Ji Lim, Alexandra T Barbour, Arthur J Zaug, Karen J Goodrich, Allison E McKay, Deborah S Wuttke, Thomas R Cech

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

71 citing papers in PubMed, 117 citations in OpenAlex.

  1. Mechanisms and disease relevance of DNA break repair pathway choice.Nature reviews. Molecular cell biology · 2026
    Review
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11 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

7 authors at 2 institutions in 1 country.

Ci Ji LimDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA.ORCID 0000-0003-3327-1926
Alexandra T BarbourDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA.ORCID 0000-0003-0847-8546
Arthur J ZaugDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA.ORCID 0000-0001-7324-803X
Karen J GoodrichDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA.ORCID 0000-0003-3301-7725
Allison E McKayDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA.ORCID 0000-0003-0288-9731
Deborah S WuttkeDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA. thomas.cech@colorado.edu deborah.wuttke@colorado.edu.ORCID 0000-0002-8158-8795
Thomas R CechDepartment of Biochemistry, University of Colorado Boulder, Boulder, CO 80303, USA. thomas.cech@colorado.edu deborah.wuttke@colorado.edu.ORCID 0000-0001-7338-3389
University of Colorado Boulder · USHoward Hughes Medical Institute · US

Funding

TRAINING IN SIGNAL TRANSDUCTION &CELL CYCLE REGULATIONT32GM008759 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI AHN, NATALIE G. · 2000 to 2020
$5.9M
SINGLE STRANDED DNA RECOGNITION IN TELOMERESR01GM059414 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI WUTTKE, DEBORAH S. · 1999 to 2015
$3.7M
TERT Promoter Mutations and Telomerase Reactivation in Cancer CellsR01GM099705 · NIGMS · UNIVERSITY OF COLORADO · PI CECH, THOMAS ROBERT · 2012 to 2019
$1.4M
RPA and RPA-like Complexes at TelomeresR01GM139274 · NIGMS · UNIVERSITY OF COLORADO · PI WUTTKE, DEBORAH S. · 2020 to 2023
$1.2M
Structural understanding of human shelterin complex assembly at telomere and its regulation mechanism of telomerase activityR00GM131023 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI LIM, CI JI · 2020 to 2022
$730k
Structural understanding of human shelterin complex assembly at telomere and its regulation mechanism of telomerase activityK99GM131023 · NIGMS · UNIVERSITY OF COLORADO · PI LIM, CI JI · 2019 to 2020
$200k
NIGMS NIH HHS K99 GM131023NIGMS NIH HHS R00 GM131023NIGMS NIH HHS R01 GM059414NIGMS NIH HHS R01 GM099705NIGMS NIH HHS R01 GM139274NIGMS NIH HHS T32 GM008759
6 · The paper itself

Abstract

The CTC1-STN1-TEN1 (CST) complex is essential for telomere maintenance and resolution of stalled replication forks genome-wide. Here, we report the 3.0-angstrom cryo-electron microscopy structure of human CST bound to telomeric single-stranded DNA (ssDNA), which assembles as a decameric supercomplex. The atomic model of the 134-kilodalton CTC1 subunit, built almost entirely de novo, reveals the overall architecture of CST and the DNA-binding anchor site. The carboxyl-terminal domain of STN1 interacts with CTC1 at two separate docking sites, allowing allosteric mediation of CST decamer assembly. Furthermore, ssDNA appears to staple two monomers to nucleate decamer assembly. CTC1 has stronger structural similarity to Replication Protein A than the expected similarity to yeast Cdc13. The decameric structure suggests that CST can organize ssDNA analogously to the nucleosome's organization of double-stranded DNA.

Indexed as

Telomere HomeostasisCryoelectron MicroscopyDNA, Single-StrandedHEK293 CellsHumansMultiprotein ComplexesProtein BindingProtein DomainsProtein MultimerizationReplication Protein ATelomereTelomere-Binding ProteinsCtc1 protein, humanDNA, Single-StrandedMultiprotein ComplexesReplication Protein AStn1 protein, humanTelomere-Binding ProteinsTen1 protein, human

Identifiers

PMID32499435
PMCPMC7559292
OpenAlexW3033318436

What OpenQuestion holds

Textmetadata
LicenceTDM
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.