Evidence map›Paper›PMID 10575032›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

The ETS domain factor Pet-1 is an early and precise marker of central serotonin neurons and interacts with a conserved element in serotonergic genes.

T Hendricks, N Francis, D Fyodorov, E S Deneris

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed
1.4field-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

153 citing papers in PubMed, 308 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Serotonin neurons are necessary for tonic sodium intake inhibition.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  5. Article
  6. Article
  7. The periaxonal space as a conduit for cerebrospinal fluid flow to peripheral organs.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. iScience · 2023
    Article
  12. Article
  13. Review
  14. Single Nuclei Analyses Reveal Transcriptional Profiles and Marker Genes for Diverse Supraspinal Populations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

93 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

4 authors at 1 institution in 1 country.

T HendricksCase Western Reserve University, Department of Neurosciences, School of Medicine, Cleveland, Ohio 44106, USA.
N Francis
D Fyodorov
E S Deneris
Case Western Reserve University · US

Funding

REGULATION OF NEURONAL NICOTINIC ACETYLOCHOLINE RECEPTORR01NS029123 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI DENERIS, EVAN S · 1991 to 2006
$2.0M
A NEW ETS FACTOR IN THE SEROTONERGIC SYSTEMR03MH058926 · NIMH · CASE WESTERN RESERVE UNIVERSITY · PI DENERIS, EVAN S · 1998 to 1999
–
NIMH NIH HHS MH58926NINDS NIH HHS NS29123NINDS NIH HHS R01 NS029123
6 · The paper itself

Abstract

Serotonin (5-HT) plays a crucial neuromodulatory role in numerous physiological and behavioral functions, and dysfunction of the serotonergic system has been implicated in several psychiatric disorders. Despite the widespread importance of the central serotonergic neurotransmitter system, little is known about the molecular mechanisms controlling the development of 5-HT neurons. We previously identified an ETS domain transcription factor, Pet-1, that is expressed in a small number of tissues, including the brain. Here, we show that expression of Pet-1 RNA in the brain is restricted to, and marks, the entire rostrocaudal extent of rat serotonergic hindbrain raphe nuclei. Remarkably, Pet-1 RNA colocalizes with tryptophan hydroxylase-positive neurons in raphe nuclei but not with their nonserotonergic neuron or non-neuronal neighbors. Pet-1 RNA is limited to two domains in the developing hindbrain, which precedes the appearance of 5-HT in each domain by approximately a half day. Conserved Pet-1 binding sites are present in or near the promoter regions of the human and mouse 5-HT1a receptor, serotonin transporter, tryptophan hydroxylase, and aromatic L-amino acid decarboxylase genes whose expression is characteristic of the serotonergic neuron phenotype. These sites are capable of supporting transcriptional activation through interactions with the Pet-1 ETS domain and can function as enhancers. Together, our findings establish Pet-1 as an early and precise marker of 5-HT neurons and suggest that it functions specifically in the differentiation and maintenance of these neurons.

Indexed as

Transcription FactorsAnimalsBinding SitesBiomarkersBrainConserved SequenceEmbryo, MammalianGene ExpressionNeuronsProto-Oncogene ProteinsRaphe NucleiRatsRats, Sprague-DawleyRhombencephalonRNASerotoninBiomarkersFev protein, mouseFev protein, ratProto-Oncogene ProteinsRNASerotoninTranscription FactorsTyrosine 3-Monooxygenase

Identifiers

PMID10575032
PMCPMC6782418
OpenAlexW2152069082

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.