Evidence map›Paper›PMID 36934410›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2023

SAMHD1 restricts the deoxyguanosine triphosphate pool contributing to telomere stability in telomerase-positive cells.

Giulia D'Aronco, Paola Ferraro, Valentina Sassano, Claudia Dagostino, Melissa Biancotto, Elisa Palumbo, Ettore Presot, Antonella Russo, Vera Bianchi, Chiara Rampazzo

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. SAMHD1 restricts the deoxyguanosine triphosphate pool contributing to telomere stability in telomerase-positive cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
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

10 authors at 1 institution in 1 country.

Giulia D'AroncoDepartment of Biology, University of Padova, Padova, Italy.
Paola FerraroDepartment of Biology, University of Padova, Padova, Italy.
Valentina SassanoDepartment of Biology, University of Padova, Padova, Italy.
Claudia DagostinoDepartment of Biology, University of Padova, Padova, Italy.
Melissa BiancottoDepartment of Biology, University of Padova, Padova, Italy.
Elisa PalumboDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Ettore PresotDepartment of Biology, University of Padova, Padova, Italy.
Antonella RussoDepartment of Molecular Medicine, University of Padova, Padova, Italy.ORCID https://orcid.org/0000-0001-6691-257X
Vera BianchiDepartment of Biology, University of Padova, Padova, Italy.
Chiara RampazzoDepartment of Biology, University of Padova, Padova, Italy.ORCID https://orcid.org/0000-0002-1092-2653
University of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SAMHD1 (Sterile alpha motif and histidine/aspartic acid domain-containing protein 1) is a dNTP triphosphohydrolase crucial in the maintenance of balanced cellular dNTP pools, which support genome integrity. In SAMHD1 deficient fibroblasts isolated from Aicardi-Goutières Syndrome (AGS) patients, all four DNA precursors are increased and markedly imbalanced with the largest effect on dGTP, a key player in the modulation of telomerase processivity. Here, we present data showing that SAMHD1, by restricting the dGTP pool, contributes to telomere maintenance in hTERT-immortalized human fibroblasts from AGS patients as well as in telomerase positive cancer cell lines. Only in cells expressing telomerase, the lack of SAMHD1 causes excessive lengthening of telomeres and telomere fragility, whereas primary fibroblasts lacking both SAMHD1 and telomerase enter normally into senescence. Telomere lengthening observed in SAMHD1 deficient but telomerase proficient cells is a gradual process, in accordance with the intrinsic property of telomerase of adding only a few tens of nucleotides for each cycle. Therefore, only a prolonged exposure to high dGTP content causes telomere over-elongation. hTERT-immortalized AGS fibroblasts display also high fragility of chromosome ends, a marker of telomere replication stress. These results not only demonstrate the functional importance of dGTP cellular level but also reveal the critical role played by SAMHD1 in restraining telomerase processivity and safeguarding telomere stability.

Indexed as

Monomeric GTP-Binding ProteinsSAM Domain and HD Domain-Containing Protein 1TelomeraseDeoxyguanine NucleotidesHumansTelomereDeoxyguanine Nucleotidesdeoxyguanosine triphosphateMonomeric GTP-Binding ProteinsSAM Domain and HD Domain-Containing Protein 1SAMHD1 protein, humanTelomeraseAicardi-Goutières syndrome (AGS)deoxynucleotide metabolismdeoxynucleotide pool imbalancesterile alpha motif and HD domain containing protein 1 (SAMHD1)telomere maintenance

Identifiers

PMID36934410
PMCPMC11977530
OpenAlexW4327857218

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.