Evidence map›Paper›PMID 33137089›Full record

Observational studyPLoS genetics2020

Differential transcript usage in the Parkinson's disease brain.

Fiona Dick, Gonzalo S Nido, Guido Werner Alves, Ole-Bjørn Tysnes, Gry Hilde Nilsen, Christian Dölle, Charalampos Tzoulis

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Dynamic changes in mRNA isoform usage during human retinal development.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Characterisation of the Function of a SINE-VNTR-Frontiers in molecular neuroscience · 2022
    Article
  15. RNA Modifications and RNA Metabolism in Neurological Disease Pathogenesis.International journal of molecular sciences · 2021
    Review
  16. Article
  17. 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

7 authors at 2 institutions in 1 country.

Fiona DickNeuro-SysMed, Department of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-4728-9345
Gonzalo S NidoNeuro-SysMed, Department of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-1766-4108
Guido Werner AlvesThe Norwegian Center for Movement Disorders and Department of Neurology, Stavanger University Hospital, Stavanger, Norway.ORCID 0000-0003-0630-2870
Ole-Bjørn TysnesNeuro-SysMed, Department of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-7230-6426
Gry Hilde NilsenNeuro-SysMed, Department of Neurology, Haukeland University Hospital, Bergen, Norway.
Christian DölleNeuro-SysMed, Department of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0003-2427-8130
Charalampos TzoulisNeuro-SysMed, Department of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0003-0341-5191
Haukeland University Hospital · NOStavanger University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies of differential gene expression have identified several molecular signatures and pathways associated with Parkinson's disease (PD). The role of isoform switches and differential transcript usage (DTU) remains, however, unexplored. Here, we report the first genome-wide study of DTU in PD. We performed RNA sequencing following ribosomal RNA depletion in prefrontal cortex samples of 49 individuals from two independent case-control cohorts. DTU was assessed using two transcript-count based approaches, implemented in the DRIMSeq and DEXSeq tools. Multiple PD-associated DTU events were detected in each cohort, of which 23 DTU events in 19 genes replicated across both patient cohorts. For several of these, including THEM5, SLC16A1 and BCHE, DTU was predicted to have substantial functional consequences, such as altered subcellular localization or switching to non-protein coding isoforms. Furthermore, genes with PD-associated DTU were enriched in functional pathways previously linked to PD, including reactive oxygen species generation and protein homeostasis. Importantly, the vast majority of genes exhibiting DTU were not differentially expressed at the gene-level and were therefore not identified by conventional differential gene expression analysis. Our findings provide the first insight into the DTU landscape of PD and identify novel disease-associated genes. Moreover, we show that DTU may have important functional consequences in the PD brain, since it is predicted to alter the functional composition of the proteome. Based on these results, we propose that DTU analysis is an essential complement to differential gene expression studies in order to provide a more accurate and complete picture of disease-associated transcriptomic alterations.

Indexed as

Case-Control StudiesComputational BiologyGenome-Wide Association StudyHumansModels, GeneticParkinson DiseasePrefrontal CortexProtein IsoformsRNA-SeqTranscriptomeProtein Isoforms

Identifiers

PMID33137089
PMCPMC7660910
OpenAlexW3097769501

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.