Evidence map›Paper›PMID 31019071›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Telomere DNA G-quadruplex folding within actively extending human telomerase.

Linnea I Jansson, Jendrik Hentschel, Joseph W Parks, Terren R Chang, Cheng Lu, Rishika Baral, Clive R Bagshaw, Michael D Stone

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
6.8field-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

58 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
  2. Article
  3. Cancer-associated TRF1 mutations alter PARP1 interaction dynamics: an in silico study.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
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  6. Review
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  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. G-quadruplex propensity inNAR genomics and bioinformatics · 2024
    Article
  18. Combating multidrug-resistance inNAR molecular medicine · 2024
    Article
  19. Article
  20. Review
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

8 authors at 2 institutions in 1 country.

Linnea I JanssonMolecular, Cell and Developmental Biology Department, University of California, Santa Cruz, CA 95064.
Jendrik HentschelChemistry and Biochemistry Department, University of California, Santa Cruz, CA 95064.
Joseph W ParksInvitae, San Francisco, CA 94103.
Terren R ChangChemistry and Biochemistry Department, University of California, Santa Cruz, CA 95064.
Cheng LuDepartment of Protein Chemistry, Genentech Inc., South San Francisco, CA 94080.
Rishika BaralChemistry and Biochemistry Department, University of California, Santa Cruz, CA 95064.
Clive R BagshawChemistry and Biochemistry Department, University of California, Santa Cruz, CA 95064.
Michael D StoneChemistry and Biochemistry Department, University of California, Santa Cruz, CA 95064; mds@ucsc.edu.
University of California, Santa Cruz · USInvitae (United States) · US

Funding

Structure and dynamics of the Tetrahymena telomerase ribonucleoproteinR01GM095850 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI STONE, MICHAEL D · 2011 to 2023
$4.4M
Training Program/Molecular/Cell/Developmental BiologyT32GM008646 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI STROME, SUSAN · 1999 to 2018
$3.7M
The roles of telomerase and non-coding RNA in cancerK00CA212439 · NCI · UNIVERSITY OF COLORADO · PI JANSSON-FRITZBERG, LINNEA · 2018 to 2022
$432k
The roles of telomerase and non-coding RNA in cancerF99CA212439 · NCI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI JANSSON-FRITZBERG, LINNEA · 2016 to 2017
$73k
NCI NIH HHS F99 CA212439NCI NIH HHS K00 CA212439NIGMS NIH HHS R01 GM095850NIGMS NIH HHS T32 GM008646
6 · The paper itself

Abstract

Telomerase reverse transcribes short guanine (G)-rich DNA repeat sequences from its internal RNA template to maintain telomere length. G-rich telomere DNA repeats readily fold into G-quadruplex (GQ) structures in vitro, and the presence of GQ-prone sequences throughout the genome introduces challenges to replication in vivo. Using a combination of ensemble and single-molecule telomerase assays, we discovered that GQ folding of the nascent DNA product during processive addition of multiple telomere repeats modulates the kinetics of telomerase catalysis and dissociation. Telomerase reactions performed with telomere DNA primers of varying sequence or using GQ-stabilizing K

Indexed as

DNADNA PrimersFluorescence Resonance Energy TransferG-QuadruplexesHumansKineticsShelterin ComplexTelomeraseTelomereTelomere-Binding ProteinsACD protein, humanDNADNA PrimersShelterin ComplexTelomeraseTelomere-Binding ProteinsDNA structureG quadruplexPOT1–TPP1telomerasetelomere

Identifiers

PMID31019071
PMCPMC6510993
OpenAlexW2951699836

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.