Evidence map›Paper›PMID 20181818›Full record

ArticleMolecular pharmacology2010

High-throughput multiplexed transcript analysis yields enhanced resolution of 5-hydroxytryptamine 2C receptor mRNA editing profiles.

Michael V Morabito, Randi J Ulbricht, Richard T O'Neil, David C Airey, Pengcheng Lu, Bing Zhang, Lily Wang, Ronald B Emeson

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmacology, 2010. 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
1.5field-weighted citation impact, top 19% 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, 32 citations in OpenAlex.

  1. Interaction of the Vagus Nerve and Serotonin in the Gut-Brain Axis.International journal of molecular sciences · 2025
    Review
  2. Article
  3. Review
  4. Review
  5. Quantitative Analysis of Adenosine-to-Inosine RNA Editing.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. A Fluorescent Adenosine Analogue as a Substrate for an A-to-I RNA Editing Enzyme.Angewandte Chemie (International ed. in English) · 2015
    Article
  15. Article
  16. Article
  17. Article
  18. Functional status of the serotonin 5-HT2C receptor (5-HT2CR) drives interlocked phenotypes that precipitate relapse-like behaviors in cocaine dependence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    Article
  19. Serotonin 2c receptor RNA editing in major depression and suicide.The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry · 2013
    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.

Michael V MorabitoDepartment of Pharmacology, Vanderbilt University School of Medicine, 465 21st Avenue South, Nashville, TN 37232-8548, USA.
Randi J Ulbricht
Richard T O'Neil
David C Airey
Pengcheng Lu
Bing Zhang
Lily Wang
Ronald B Emeson
Vanderbilt University · US

Funding

Project 6 Interactions of Serotonin and Circadian Signaling NetworksP50MH078028 · NIMH · VANDERBILT UNIVERSITY · PI SNODDY, JAY R · 2007 to 2011
$9.8M
Program in NeurogenomicsT32MH065215 · NIMH · VANDERBILT UNIVERSITY · PI ROGER J COLBRAN · 2002 to 2026
$6.4M
Genetic analysis of Htr2c RNA editing in amygdalaR21MH077942 · NIMH · VANDERBILT UNIVERSITY · PI AIREY, DAVID C · 2007 to 2008
$376k
NIMH NIH HHS P50 MH078028NIMH NIH HHS P50-MH078028NIMH NIH HHS R21 MH077942NIMH NIH HHS R21-MH77942NIMH NIH HHS T32 MH065215
6 · The paper itself

Abstract

RNA editing is a post-transcriptional modification in which adenosine residues are converted to inosine (adenosine-to-inosine editing). Commonly used methodologies to quantify RNA editing levels involve either direct sequencing or pyrosequencing of individual cDNA clones. The limitations of these methods lead to a small number of clones characterized in comparison to the number of mRNA molecules in the original sample, thereby producing significant sampling errors and potentially erroneous conclusions. We have developed an improved method for quantifying RNA editing patterns that increases sequence analysis to an average of more than 800,000 individual cDNAs per sample, substantially increasing accuracy and sensitivity. Our method is based on the serotonin 2C receptor (5-hydroxytryptamine(2C); 5HT(2C)) transcript, an RNA editing substrate in which up to five adenosines are modified. Using a high-throughput multiplexed transcript analysis, we were able to quantify accurately the expression of twenty 5HT(2C) isoforms, each representing at least 0.25% of the total 5HT(2C) transcripts. Furthermore, this approach allowed the detection of previously unobserved changes in 5HT(2C) editing in RNA samples isolated from different inbred mouse strains and dissected brain regions, as well as editing differences in alternatively spliced 5HT(2C) variants. This approach provides a novel and efficient strategy for large-scale analyses of RNA editing and may prove to be a valuable tool for uncovering new information regarding editing patterns in specific disease states and in response to pharmacological and physiological perturbation, further elucidating the impact of 5HT(2C) RNA editing on central nervous system function.

Indexed as

RNA EditingAnimalsBase SequenceDNA, ComplementaryMaleMiceMice, Inbred StrainsReceptor, Serotonin, 5-HT2CRNA, MessengerDNA, ComplementaryReceptor, Serotonin, 5-HT2CRNA, Messenger

Identifiers

PMID20181818
PMCPMC2879922
OpenAlexW2030605994

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.