Evidence map›Paper›PMID 34077532›Full record

ArticleHuman molecular genetics2021

Toxicity of pathogenic ataxin-2 in Drosophila shows dependence on a pure CAG repeat sequence.

Leeanne McGurk, Olivia M Rifai, Oksana Shcherbakova, Alexandra E Perlegos, China N Byrns, Faith R Carranza, Henry W Zhou, Hyung-Jun Kim, Yongqing Zhu, Nancy M Bonini

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Aberrant NSUN1 activity connects mLife science alliance · 2026
    Article
  5. Review
  6. PolyQ-Expansion of Ataxin-2 Disrupts Microtubule Stability and Impairs Axon Outgrowth.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. AreNeural regeneration research · 2022
    Article
  12. 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 2 institutions in 2 countries.

Leeanne McGurkDivision of Cell & Developmental Biology, School of Life Sciences, University of Dundee, Dundee, UK.
Olivia M RifaiDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Oksana ShcherbakovaDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Alexandra E PerlegosNeurosciences Graduate Group, University of Pennsylvania, Philadelphia, PA, USA.
China N ByrnsNeurosciences Graduate Group, University of Pennsylvania, Philadelphia, PA, USA.
Faith R CarranzaDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Henry W ZhouDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Hyung-Jun KimDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Yongqing ZhuDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Nancy M BoniniDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
University of Pennsylvania · USUniversity of Dundee · GB

Funding

TRAINING PROGRAM IN CELL AND MOLECULAR BIOLOGYT32GM007229 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BARTOLOMEI, MARISA S. · 1985 to 2023
$14.0M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Cale Whitworth · 2014 to 2026
$13.5M
Training in Alzheimer’s and Age-Related Neurodegenerative DiseasesT32AG000255 · NIA · UNIVERSITY OF PENNSYLVANIA · PI ALICE S CHEN-PLOTKIN, VIRGINIA M LEE · 1997 to 2026
$12.5M
Molecular Genetic Insight into Neurodegenerative Disease from DrosophilaR35NS097275 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI BONINI, NANCY M · 2017 to 2024
$6.0M
The in vivo role of m6A RNA modification in Cellular Stress, Aging, and Neurological ­DiseaseF31AG063470 · NIA · UNIVERSITY OF PENNSYLVANIA · PI PERLEGOS, ALEXANDRA EMILY · 2019 to 2021
$124k
Novel mechanisms of the glial response to traumatic brain injury: dissecting the role of Ets21c in a Drosophila modelF31NS111868 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI BYRNS, CHINA · 2019 to 2020
$78k
NIA NIH HHS F31 AG063470NIA NIH HHS T32 AG000255NIGMS NIH HHS T32 GM007229NIH HHS P40 OD018537NINDS NIH HHS F31 NS111868NINDS NIH HHS R35 NS097275
6 · The paper itself

Abstract

Spinocerebellar ataxia type 2 is a polyglutamine (polyQ) disease associated with an expanded polyQ domain within the protein product of the ATXN2 gene. Interestingly, polyQ repeat expansions in ATXN2 are also associated with amyotrophic lateral sclerosis (ALS) and parkinsonism depending upon the length of the polyQ repeat expansion. The sequence encoding the polyQ repeat also varies with disease presentation: a pure CAG repeat is associated with SCA2, whereas the CAG repeat in ALS and parkinsonism is typically interrupted with the glutamine encoding CAA codon. Here, we asked if the purity of the CAG sequence encoding the polyQ repeat in ATXN2 could impact the toxicity of the ataxin-2 protein in vivo in Drosophila. We found that ataxin-2 encoded by a pure CAG repeat conferred toxicity in the retina and nervous system, whereas ataxin-2 encoded by a CAA-interrupted repeat or CAA-only repeat failed to confer toxicity, despite expression of the protein at similar levels. Furthermore, the CAG-encoded ataxin-2 protein aggregated in the fly eye, while ataxin-2 encoded by either a CAA/G or CAA repeat remained diffuse. The toxicity of the CAG-encoded ataxin-2 protein was also sensitive to the translation factor eIF4H, a known modifier of the toxic GGGGCC repeat in flies. These data indicate that ataxin-2 encoded by a pure CAG versus interrupted CAA/G polyQ repeat domain is associated with differential toxicity, indicating that mechanisms associated with the purity of the sequence of the polyQ domain contribute to disease.

Indexed as

Amyotrophic Lateral SclerosisAtaxin-2Spinocerebellar AtaxiasAnimalsAtaxin-3AtaxinsDisease Models, AnimalDrosophilaTrinucleotide Repeat ExpansionAtaxin-2Ataxin-3Ataxins

Identifiers

PMID34077532
PMCPMC8444453
OpenAlexW3165318719

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.