Evidence map›Paper›PMID 26725726›Full record

ArticleScientific reports2016

PARP6 is a Regulator of Hippocampal Dendritic Morphogenesis.

Jeffrey Y Huang, Kang Wang, Anke Vermehren-Schmaedick, John P Adelman, Michael S Cohen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Genome-wide profiling of RNA 2'-bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Review
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  10. Functional roles of ADP-ribosylation writers, readers and erasers.Frontiers in cell and developmental biology · 2022
    Review
  11. Article
  12. Article
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  14. Review
  15. Article
  16. Article
  17. Article
  18. Collapsin Response Mediator Protein-2 Ameliorates Sevoflurane-Mediated Neurocyte Injury by Targeting PI3K-mTOR-S6K Pathway.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  19. Review
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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

5 authors at 2 institutions in 1 country.

Jeffrey Y HuangDepartment of Physiology and Pharmacology, Oregon Health &Science University, Portland, Oregon 97210, United States.
Kang WangVollum Institute, Oregon Health &Science University, Portland, Oregon 97210, United States.
Anke Vermehren-SchmaedickDepartment of Physiology and Pharmacology, Oregon Health &Science University, Portland, Oregon 97210, United States.
John P AdelmanVollum Institute, Oregon Health &Science University, Portland, Oregon 97210, United States.
Michael S CohenDepartment of Physiology and Pharmacology, Oregon Health &Science University, Portland, Oregon 97210, United States.
Oregon Health & Science University · USVollum Institute · US

Funding

Decoding protein MARylation networks in astrocytes using chemical biology approachesR01NS088629 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI COHEN, MICHAEL S · 2014 to 2024
$4.2M
NINDS NIH HHS NS088629NINDS NIH HHS R01 NS088629
6 · The paper itself

Abstract

Mono-ADP-ribosylation (MARylation) of mammalian proteins was first described as a post-translational modification catalyzed by bacterial toxins. It is now known that endogenous MARylation occurs in mammalian cells and is catalyzed by 11 members of the poly-ADP-ribose polymerase (PARP) family of proteins (17 in humans). The physiological roles of these PARPs remain largely unknown. Here we demonstrate that PARP6, a neuronally enriched PARP that catalyzes MARylation, regulates hippocampal dendrite morphogenesis, a process that is critical for proper neural circuit formation during development. Knockdown of PARP6 significantly decreased dendritic complexity in embryonic rat hippocampal neurons in culture and in vivo. Expression of wild-type PARP6 increased dendritic complexity; conversely, expression of a catalytically inactive PARP6 mutant, or a cysteine-rich domain deletion mutant that has significantly reduced catalytic activity, decreased dendritic complexity. The identification of PARP6 as a regulator of dendrite morphogenesis supports a role for MARylation in neurons during development.

Indexed as

ADP Ribose TransferasesAnimalsCells, CulturedDendritesGene ExpressionHippocampusMice, Inbred C57BLMorphogenesisNeurogenesisPoly(ADP-ribose) PolymerasesPrimary Cell CultureProtein DomainsProtein Processing, Post-TranslationalRats, Sprague-DawleyADP Ribose TransferasesPARP6 protein, mousePoly(ADP-ribose) Polymerases

Identifiers

PMID26725726
PMCPMC4698753
OpenAlexW2414493819

What OpenQuestion holds

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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.