Evidence map›Paper›PMID 32954964›Full record

ArticleRNA biology2021

Noncanonical cytoplasmic poly(A) polymerases regulate RNA levels, alternative RNA processing, and synaptic plasticity but not hippocampal-dependent behaviours.

Fernanda Mansur, Juan Marcos Alarcon, Emily E Stackpole, Ruijia Wang, Joel D Richter

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Terminal nucleotidyltransferaseRNA (New York, N.Y.) · 2025
    Article
  3. Article
  4. Review
  5. RNA in axons, dendrites, synapses and beyond.Frontiers in molecular neuroscience · 2024
    Review
  6. 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

5 authors at 2 institutions in 1 country.

Fernanda MansurProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Juan Marcos AlarconDepartment of Pathology, SUNY Downstate Health Sciences University, Brooklyn, New York, USA.
Emily E StackpoleProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Ruijia WangProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Joel D RichterProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
University of Massachusetts Chan Medical School · USSUNY Downstate Health Sciences University · US

Funding

Strategies to rescue PI3K dysregulation in Fragile X SyndromeU54HD082013 · NICHD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RICHTER, JOEL D · 2014 to 2019
$10.2M
POLYADENYLATION AND TRANSLATIONAL CONTROLR01GM046779 · NIGMS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI RICHTER, JOEL D · 1992 to 2022
$7.7M
FMRP Regulation of Gene ExpressionR01GM135087 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUBER, KIMBERLY M., RICHTER, JOEL D · 2020 to 2023
$2.4M
Experience-dependent Modulation of Synaptic Circuits in the HippocampusR21NS091830 · NINDS · SUNY DOWNSTATE MEDICAL CENTER · PI ALARCON, JUAN MARCOS · 2015 to 2016
$456k
NICHD NIH HHS U54 HD082013NIGMS NIH HHS R01 GM046779NIGMS NIH HHS R01 GM135087NINDS NIH HHS R21 NS091830
6 · The paper itself

Abstract

Noncanonical poly(A) polymerases are frequently tethered to mRNA 3' untranslated regions and regulate poly(A) tail length and resulting translation. In the brain, one such poly(A) polymerase is Gld2, which is anchored to mRNA by the RNA-binding protein CPEB1 to control local translation at postsynaptic regions. Depletion of CPEB1 or Gld2 from the mouse hippocampus results in a deficit in long-term potentiation (LTP), but only depletion of CPEB1 alters animal behaviour. To test whether a related enzyme, Gld4, compensates for the lack of Gld2, we separately or simultaneously depleted both proteins from hippocampal area CA1 and again found little change in animal behaviour, but observed a deficit in LTP as well as an increase in long-term depression (LTD), two forms of protein synthesis-dependent synaptic plasticity. RNA-seq data from Gld2, Gld4, and Gld2/Gld4-depleted hippocampus show widespread changes in steady state RNA levels, alternative splicing, and alternative poly(A) site selection. Many of the RNAs subject to these alterations encode proteins that mediate synaptic function, suggesting a molecular foundation for impaired synaptic plasticity.

Indexed as

RNA Processing, Post-Transcriptional3' Untranslated RegionsAnimalsAvoidance LearningCA1 Region, HippocampalGene Expression RegulationInjections, IntraventricularIsoenzymesLong-Term PotentiationMaleMaze LearningMiceMice, Inbred C57BLmRNA Cleavage and Polyadenylation FactorsNeuronal PlasticityObsessive Behavior3' Untranslated RegionsCpeb1 protein, mouseGld2 protein, mouseIsoenzymesmRNA Cleavage and Polyadenylation FactorsPolynucleotide AdenylyltransferaseRNA, MessengerRNA, Small InterferingTranscription Factorsalternative RNA processinganimal behaviourNoncanonical poly(A) polymeraseRNA-seqsynaptic plasticity

Identifiers

PMID32954964
PMCPMC8216208
OpenAlexW3087125446

What Socratic holds

Textmetadata
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 Socratic graph.