Evidence map›Paper›PMID 36858083›Full record

ArticleMolecular and cellular neurosciences2023

The Tardigrade damage suppressor protein Dsup promotes DNA damage in neurons.

Rocio Diaz Escarcega, Abhijeet A Patil, Matthew D Meyer, Jose F Moruno-Manchon, Alexander D Silvagnoli, Louise D McCullough, Andrey S Tsvetkov

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
14.5field-weighted citation impact, top 1% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Tardigrade Dsup extendsScience advances · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mitigating age-related somatic mutation burden.Trends in molecular medicine · 2023
    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

7 authors at 2 institutions in 1 country.

Rocio Diaz EscarcegaDepartment of Neurology, The University of Texas McGovern Medical School at Houston, TX 77030, United States of America.
Abhijeet A PatilDepartment of Neurology, The University of Texas McGovern Medical School at Houston, TX 77030, United States of America.
Matthew D MeyerShared Equipment Authority, Rice University, Houston, TX 77005, United States of America.
Jose F Moruno-ManchonDepartment of Neurology, The University of Texas McGovern Medical School at Houston, TX 77030, United States of America.
Alexander D SilvagnoliDepartment of Neurology, The University of Texas McGovern Medical School at Houston, TX 77030, United States of America.
Louise D McCulloughDepartment of Neurology, The University of Texas McGovern Medical School at Houston, TX 77030, United States of America; The University of Texas Graduate School of Biomedical Sciences, Houston, TX 77030, United States of America.
Andrey S TsvetkovDepartment of Neurology, The University of Texas McGovern Medical School at Houston, TX 77030, United States of America; The University of Texas Graduate School of Biomedical Sciences, Houston, TX 77030, United States of America; UTHealth Consortium on Aging, The University of Texas McGovern Medical School, Houston, TX 77030, United States of America. Electronic address: andrey.s.tsvetkov@uth.tmc.edu.
Rice University · USThe University of Texas Health Science Center at Houston · US

Funding

NAAG Peptidase, Chemobrain, and Alzheimer's diseaseR21AG067204 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TSVETKOV, ANDREY · 2020 to 2020
$428k
NIA NIH HHS R21 AG067204
6 · The paper itself

Abstract

Tardigrades are microscopic invertebrates, which are capable of withstanding extreme environmental conditions, including high levels of radiation. A Tardigrade protein, Dsup (Damage Suppressor), protects the Tardigrade's DNA during harsh environmental stress and X-rays. When expressed in cancer cells, Dsup protects DNA from single- and double-strand breaks (DSBs) induced by radiation, increases survival of irradiated cells, and protects DNA from reactive oxygen species. These unusual properties of Dsup suggested that understanding how the protein functions may help in the design of small molecules that could protect humans during radiotherapy or space travel. Here, we investigated if Dsup is protective in cortical neurons cultured from rat embryos. We discovered that, in cortical neurons, the codon-optimized Dsup localizes to the nucleus and, surprisingly, promotes neurotoxicity, leading to neurodegeneration. Unexpectedly, we found that Dsup expression results in the formation of DNA DSBs in cultured neurons. With electron microscopy, we discovered that Dsup promotes chromatin condensation. Unlike Dsup's protective properties in cancerous cells, in neurons, Dsup promotes neurotoxicity, induces DNA damage, and rearranges chromatin. Neurons are sensitive to Dsup, and Dsup is a doubtful surrogate for DNA protection in neuronal cells.

Indexed as

ChromatinDNA DamageAnimalsDNADNA Breaks, Double-StrandedHumansNeuronsRatsChromatinDNADNA damageDsupNeurodegenerationNeurotoxicityThe Tardigrade

Identifiers

PMID36858083
PMCPMC10247392
OpenAlexW4322487406

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.