Evidence map›Paper›PMID 27113499›Full record

ArticleBiological psychiatry2017

A Comprehensive Analysis of Cell Type-Specific Nuclear RNA From Neurons and Glia of the Brain.

Adarsh S Reddy, David O'Brien, Nilambari Pisat, Claire T Weichselbaum, Kristina Sakers, Miriam Lisci, Jasbir S Dalal, Joseph D Dougherty

Abstract read
In one paragraph

Article in Biological psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. mMolecular neurobiology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Specific expression and functions of circular RNAs.Cell death and differentiation · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Expression and function of circular RNAs in the mammalian brain.Cellular and molecular life sciences : CMLS · 2021
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. circPTN sponges miR-145-5p/miR-330-5p to promote proliferation and stemness in glioma.Journal of experimental & clinical cancer research : CR · 2019
    Article
  20. 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

8 authors at 1 institution in 1 country.

Adarsh S ReddyDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri.
David O'BrienDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri. Electronic address: jdougherty@genetics.wustl.edu.
Nilambari PisatDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri.
Claire T WeichselbaumDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri.
Kristina SakersDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri.
Miriam LisciDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri.
Jasbir S DalalDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri.
Joseph D DoughertyDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri.
Washington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
Systems and Molecular Neurobiology Training ProgramT32GM008151 · NIGMS · WASHINGTON UNIVERSITY · PI SNYDER, LAWRENCE H · 1985 to 2019
$6.5M
AN INDUCIBLE MOLECULAR MEMORY SYSTEM TO RECORD TRANSIENT STATES OF CNS CELLSU01MH109133 · NIMH · WASHINGTON UNIVERSITY · PI MITRA, ROBI D · 2015 to 2017
$3.6M
Training At The Interface of Psychology, Neuroscience, and GeneticsT32GM081739 · NIGMS · WASHINGTON UNIVERSITY · PI BARCH, DEANNA · 2007 to 2016
$2.1M
TOOLS TO ENHANCE STUDY OF REMAK SCHWANN CELLSR21NS083052 · NINDS · WASHINGTON UNIVERSITY · PI DOUGHERTY, JOSEPH D, MONK, KELLY R · 2012 to 2013
$411k
DEVELOPMENT OF A NOVEL APPROACH TO STUDY ALTERNATIVE TRANSLATION IN THE CNSR21DA038458 · NIDA · WASHINGTON UNIVERSITY · PI DOUGHERTY, JOSEPH D · 2014 to 2015
$378k
NCATS NIH HHS UL1 TR000448NCI NIH HHS P30 CA091842NIDA NIH HHS R21 DA038458NIGMS NIH HHS T32 GM008151NIGMS NIH HHS T32 GM081739NIMH NIH HHS U01 MH109133NINDS NIH HHS R21 NS083052
6 · The paper itself

Abstract

backgroundStudies in psychiatric genetics have identified >100 loci associated with disease risk, yet many of these loci are distant from protein coding genes. Recent characterization of the transcriptional landscape of cell lines and whole tissues has suggested widespread transcription in both coding and noncoding regions of the genome, including differential expression from loci that produce regulatory noncoding RNAs that function within the nucleus; however, the nuclear transcriptome of specific cell types in the brain has not been previously investigated.

methodsWe defined the nuclear transcriptional landscape of the three major cellular divisions of the nervous system using flow sorting of genetically labeled nuclei from bacTRAP mouse lines. Next, we characterized the unique expression of coding, noncoding, and intergenic RNAs in the mature mouse brain with RNA-Seq and validation with independent methods.

resultsWe found diverse expression across the cell types of all classes of RNAs, including long noncoding RNAs, several of which were confirmed as highly enriched in the nuclei of specific cell types using anatomic methods. We also discovered several examples of cell type-specific expression of tandem gene fusions, and we report the first cell type-specific expression of circular RNAs-a neuron-specific and nuclear-enriched RNA arising from the gene Hnrnpu.

conclusionsThese data provide an important resource for studies evaluating the function of various noncoding RNAs in the brain, including noncoding RNAs that may play a role in psychiatric disease.

Indexed as

TranscriptomeAnimalsBrainFemaleHeterogeneous-Nuclear Ribonucleoprotein UMaleMiceNeurogliaNeuronsOligodendrogliaRNA, Long NoncodingRNA, NuclearSequence Analysis, RNAHeterogeneous-Nuclear Ribonucleoprotein URNA, Long NoncodingRNA, NuclearCircular RNAHnrnpulincRNAMirg1ncRNANuclear

Identifiers

PMID27113499
PMCPMC4996761
OpenAlexW2285460017

What OpenQuestion holds

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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.