Evidence map›Paper›PMID 35243767›Full record

ArticleGenes, brain, and behavior2022

A mutant allele of glycoprotein M6-B (Gpm6b) facilitates behavioral flexibility but increases delay discounting.

Sandra Sanchez-Roige, Samuel A Barnes, Jazlene Mallari, Rebecca Wood, Oksana Polesskaya, Abraham A Palmer

Open access · hybridAbstract read
In one paragraph

Article in Genes, brain, and behavior, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The Stage-Based Model of Addiction-UsingInternational journal of molecular sciences · 2023
    Review
  11. 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

6 authors at 1 institution in 1 country.

Sandra Sanchez-RoigeDepartment of Psychiatry, University of California San Diego, La Jolla, California, USA.ORCID 0000-0001-6137-5699
Samuel A BarnesDepartment of Psychiatry, University of California San Diego, La Jolla, California, USA.
Jazlene MallariDepartment of Psychiatry, University of California San Diego, La Jolla, California, USA.
Rebecca WoodDepartment of Psychiatry, University of California San Diego, La Jolla, California, USA.
Oksana PolesskayaDepartment of Psychiatry, University of California San Diego, La Jolla, California, USA.
Abraham A PalmerDepartment of Psychiatry, University of California San Diego, La Jolla, California, USA.ORCID 0000-0003-3634-0747
University of California San Diego · US

Funding

Sequencing CoreP50DA037844 · NIDA · UNIVERSITY OF CHICAGO · PI SOLBERG WOODS, LEAH CATHERINE · 2014 to 2023
$27.4M
Building Bridges to Allow Cross-species Translational genetics for the Study of AddictionDP1DA054394 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SANCHEZ ROIGE, SANDRA · 2021 to 2025
$2.4M
Early postnatal disruptions to glutamate and GABA systems and their contribution to reward deficitsR01MH108653 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BARNES, SAMUEL ALAN · 2016 to 2020
$2.0M
NIDA NIH HHS DP1 DA054394NIDA NIH HHS DP1DA054394NIDA NIH HHS P50 DA037844NIDA NIH HHS P50DA037844NIMH NIH HHS R01 MH108653NIMH NIH HHS R01MH108653
6 · The paper itself

Abstract

The neuronal membrane glycoprotein M6B (Gpm6b) gene encodes a membrane glycoprotein that belongs to the proteolipid protein family, and is enriched in neurons, oligodendrocytes, and subset of astrocytes in the central nervous system. GPM6B is thought to play a role in neuronal differentiation, myelination, and inactivation of the serotonin transporter via internalization. Recent human genome-wide association studies (GWAS) have implicated membrane glycoproteins (both GPM6B and GPM6A) in the regulation of traits relevant to psychiatric disorders, including neuroticism, depressed affect, and delay discounting. Mouse studies have implicated Gpm6b in sensorimotor gating and regulation of serotonergic signaling. We used CRISPR to create a mutant Glycoprotein M6B (Gpm6b) allele on a C57BL/6J mouse background. Because Gpm6b is located on the X chromosome, we focused on male Gpm6b mutant mice and their wild-type littermates (WT) in two behavioral tests that measured aspects of impulsive or flexible decision-making. We found that Gpm6b deletion caused deficits in a delay discounting task. In contrast, reward sensitivity was enhanced thereby facilitating behavioral flexibility and improving performance in the probabilistic reversal learning task. Taken together these data further delineate the role of Gpm6b in decision making behaviors that are relevant to multiple psychiatric disorders.

Indexed as

Delay DiscountingMembrane GlycoproteinsNerve Tissue ProteinsAllelesAnimalsGenome-Wide Association StudyHumansImpulsive BehaviorMaleMiceMice, Inbred C57BLRewardGPM6B protein, humanGpm6b protein, mouseMembrane GlycoproteinsNerve Tissue Proteinsbehavioral flexibilitydelay discountingdepressiongeneticsGPM6Bimpulsivitymouse modelpsychiatric disordersserotoninsuicide

Identifiers

PMID35243767
PMCPMC9211103
OpenAlexW4214840984

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.