Evidence map›Paper›PMID 27911744›Full record

ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Dysregulation of mRNA Localization and Translation in Genetic Disease.

Eric T Wang, J Matthew Taliaferro, Ji-Ann Lee, Indulekha P Sudhakaran, Wilfried Rossoll, Christina Gross, Kathryn R Moss, Gary J Bassell

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 113 citations in OpenAlex.

  1. Review
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  8. smFISH: Quantifying and Mapping RNA at the Single-Molecule Level.Methods in molecular biology (Clifton, N.J.) · 2026
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  19. Review
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7 more citing papers are in PubMed but not listed here.

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

8 authors at 6 institutions in 2 countries.

Eric T WangCenter for NeuroGenetics, University of Florida, Gainesville, Florida 32610, gbassel@emory.edu eric.t.wang@ufl.edu.
J Matthew TaliaferroDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307.ORCID 0000-0001-7580-1433
Ji-Ann LeeDepartment of Biological Chemistry, University of California Los Angeles, Los Angeles, California 90095-1737.ORCID 0000-0002-9069-2113
Indulekha P SudhakaranNational Centre for Biological Sciences-TIFR, Bangalore 560065, India.ORCID 0000-0002-4851-5156
Wilfried RossollDepartment of Cell Biology and Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia 30322, and.
Christina GrossDivision of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229.ORCID 0000-0001-6057-2527
Kathryn R MossDepartment of Cell Biology and Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia 30322, and.
Gary J BassellDepartment of Cell Biology and Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, Georgia 30322, and gbassel@emory.edu eric.t.wang@ufl.edu.
Emory University · USCincinnati Children's Hospital Medical Center · USManipal Academy of Higher Education · INMassachusetts Institute of Technology · USUniversity of California, Los Angeles · USUniversity of Florida · US

Funding

Ppst-transcriptional regulation of gene expression in neuromuscular diseaseDP5OD017865 · OD · UNIVERSITY OF FLORIDA · PI WANG, ERIC T · 2013 to 2017
$2.0M
NIH HHS DP5 OD017865
6 · The paper itself

Abstract

RNA-binding proteins (RBPs) acting at various steps in the post-transcriptional regulation of gene expression play crucial roles in neuronal development and synaptic plasticity. Genetic mutations affecting several RBPs and associated factors lead to diverse neurological symptoms, as characterized by neurodevelopmental and neuropsychiatric disorders, neuromuscular and neurodegenerative diseases, and can often be multisystemic diseases. We will highlight the physiological roles of a few specific proteins in molecular mechanisms of cytoplasmic mRNA regulation, and how these processes are dysregulated in genetic disease. Recent advances in computational biology and genomewide analysis, integrated with diverse experimental approaches and model systems, have provided new insights into conserved mechanisms and the shared pathobiology of mRNA dysregulation in disease. Progress has been made to understand the pathobiology of disease mechanisms for myotonic dystrophy, spinal muscular atrophy, and fragile X syndrome, with broader implications for other RBP-associated genetic neurological diseases. This gained knowledge of underlying basic mechanisms has paved the way to the development of therapeutic strategies targeting disease mechanisms.

Indexed as

AnimalsFragile X SyndromeGene Expression RegulationGenetic Predisposition to DiseaseHumansNervous System DiseasesRNA-Binding ProteinsRNA, MessengerRNA-Binding ProteinsRNA, MessengerFragile X Mental Retardation Protein (FMRP)Fragile X Syndrome (FXS)Muscleblind-like Splicing Regulator (MBNL)Myotonic Dystrophy (DM)RNA Binding Protein Fox-1 Homolog 1 (RBFOX1)Spinal Muscular Atrophy (SMA)Survival of Motor Neuron (SMN)

Identifiers

PMID27911744
PMCPMC5125209
OpenAlexW2551021318

What OpenQuestion 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 OpenQuestion graph.