Evidence map›Paper›PMID 31045220›Full record

ArticleMolecular biology and evolution2019

Serotonin Receptor 1A Variation Is Associated with Anxiety and Agonistic Behavior in Chimpanzees.

Nicky Staes, Chet C Sherwood, Hani Freeman, Sarah F Brosnan, Steven J Schapiro, William D Hopkins, Brenda J Bradley

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. The Effects ofAnimals : an open access journal from MDPI · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

7 authors at 4 institutions in 2 countries.

Nicky StaesDepartment of Anthropology, Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC.
Chet C SherwoodDepartment of Anthropology, Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC.
Hani FreemanMichale E. Keeling Center for Comparative Medicine and Research, The University of Texas MD Anderson Cancer CenterBastrop, TX.
Sarah F BrosnanMichale E. Keeling Center for Comparative Medicine and Research, The University of Texas MD Anderson Cancer CenterBastrop, TX.
Steven J SchapiroMichale E. Keeling Center for Comparative Medicine and Research, The University of Texas MD Anderson Cancer CenterBastrop, TX.
William D HopkinsNeuroscience Institute and Language Research Center, Georgia State University, Atlanta, GA.
Brenda J BradleyDepartment of Anthropology, Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC.
George Washington University · USGeorgia State University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Antwerp · BE

Funding

The National Center for Chimpanzee CareU42OD011197 · OD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ABEE, CHRISTIAN R · 2012 to 2019
$19.7M
NIH HHS U42 OD011197
6 · The paper itself

Abstract

Serotonin is a neurotransmitter that plays an important role in regulating behavior and personality in humans and other mammals. Polymorphisms in genes coding for the serotonin receptor subtype 1A (HTR1A), the serotonin transporter (SLC6A4), and the serotonin degrading enzyme monoamine oxidase A (MAOA) are associated with anxiety, impulsivity, and neurotic personality in humans. In primates, previous research has largely focused on SLC6A4 and MAOA, with few studies investigating the role of HTR1A polymorphic variation on behavior. Here, we examined variation in the coding region of HTR1A across apes, and genotyped polymorphic coding variation in a sample of 214 chimpanzees with matched measures of personality and behavior. We found evidence for positive selection at three amino acid substitution sites, one in chimpanzees-bonobos (Thr26Ser), one in humans (Phe33Val), and one in orangutans (Ala274Gly). Investigation of the HTR1A coding region in chimpanzees revealed a polymorphic site, where a C/A single nucleotide polymorphism changes a proline to a glutamine in the amino acid sequence (Pro248Gln). The substitution is located in the third intracellular loop of the receptor, a region important for serotonin signal transduction. The derived variant is the major allele in this population (frequency 0.67), and is associated with a reduction in anxiety, decreased rates of male agonistic behavior, and an increase in socio-positive behavior. These results are the first evidence that the HTR1A gene may be involved in regulating social behavior in chimpanzees and encourage further systematic investigation of polymorphic variation in other primate populations with corresponding data on behavior.

Indexed as

Agonistic BehaviorAmino Acid SequenceAnimalsAnxietyFemaleGenetic VariationMalePan troglodytesPersonalityReceptor, Serotonin, 5-HT1AReceptor, Serotonin, 5-HT1Abehavioral geneticsbehavioral tendenciesdisplaypersonalityprimates

Identifiers

PMID31045220
PMCPMC7968385
OpenAlexW2942379965

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.