Evidence map›Paper›PMID 29729314›Full record

ArticleBiochimica et biophysica acta. Molecular basis of disease2018

The human MAPT locus generates circular RNAs.

Justin R Welden, Jacob van Doorn, Peter T Nelson, Stefan Stamm

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular basis of disease, 2018. 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
1.1field-weighted citation impact, top 23% 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, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Review
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  7. Article
  8. circRNA fromInternational journal of molecular sciences · 2023
    Article
  9. Article
  10. Article
  11. Profile ofInternational journal of molecular sciences · 2022
    Article
  12. Review
  13. Circular RNAs: Emblematic Players of Neurogenesis and Neurodegeneration.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Article
  16. Review
  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

4 authors at 1 institution in 1 country.

Justin R WeldenUniversity of Kentucky, Lexington, KY 40503, United States.
Jacob van DoornUniversity of Kentucky, Lexington, KY 40503, United States.
Peter T NelsonUniversity of Kentucky, Lexington, KY 40503, United States.
Stefan StammUniversity of Kentucky, Lexington, KY 40503, United States. Electronic address: stefan@stamms-lab.net.
University of Kentucky · US

Funding

University of Kentucky Alzheimer's Disease Core Center - Biomarker CoreP30AG028383 · NIA · UNIVERSITY OF KENTUCKY · PI SCHMITT, FREDERICK · 2006 to 2020
$23.3M
Changing serotonin receptor 2C splice variants to combat spasticity after spinal cord injuryR21NS098186 · NINDS · UNIVERSITY OF KENTUCKY · PI RABCHEVSKY, ALEXANDER GEORGE, STAMM, STEFAN · 2017 to 2018
$414k
NIA NIH HHS P30 AG028383NIH HHS 1R21NS098186-01A1NIH HHS P30 AG028383NINDS NIH HHS R21 NS098186
6 · The paper itself

Abstract

The microtubule-associated protein Tau, generated by the MAPT gene is involved in dozens of neurodegenerative conditions ("tauopathies"), including Alzheimer's disease (AD) and frontotemporal lobar degeneration/frontotemporal dementia (FTLD/FTD). The pre-mRNA of MAPT is well studied and its aberrant pre-mRNA splicing is associated with frontotemporal dementia. Using a PCR screen of RNA from human brain tissues, we found that the MAPT locus generates circular RNAs through a backsplicing mechanism from exon 12 to either exon 10 or 7. MAPT circular RNAs are localized in the cytosol and contain open reading frames encoding Tau protein fragments. The MAPT exon 10 is alternatively spliced and proteins involved in its regulation, such as CLK2, SRSF7/9G8, PP1 (protein phosphatase 1) and NIPP1 (nuclear inhibitor of PP1) reduce the abundance of the circular MAPT exon 12 → 10 backsplice RNA after being transfected into cultured HEK293 cells. In summary, we report the identification of new bona fide human brain RNAs produced from the MAPT locus. These may be a component of normal human brain Tau regulation and, since the circular RNAs could generate high molecular weight proteins with multiple microtubule binding sites, they could contribute to taupathies.

Indexed as

AgedAged, 80 and overAlternative SplicingBrainExonsFemaleFrontotemporal DementiaHEK293 CellsHumansMaleMutationRNARNA, CircularRNA PrecursorsTauopathiestau ProteinsMAPT protein, humanRNARNA, CircularRNA Precursorstau ProteinsAlternative pre-mRNA splicingAlzheimer's diseaseCircular RNAsGene expressionTau

Identifiers

PMID29729314
PMCPMC6434521
OpenAlexW2801837101

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Registered trials

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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.