Evidence map›Paper›PMID 22046400›Full record

ArticlePloS one2011

Modulation ofTcf7l2 expression alters behavior in mice.

Daniel Savic, Margaret G Distler, Greta Sokoloff, Nancy A Shanahan, Stephanie C Dulawa, Abraham A Palmer, Marcelo A Nobrega

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. The Interaction BetweenBrain sciences · 2025
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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 1 institution in 1 country.

Daniel SavicDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.
Margaret G Distler
Greta Sokoloff
Nancy A Shanahan
Stephanie C Dulawa
Abraham A Palmer
Marcelo A Nobrega
University of Chicago · US

Funding

MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
PREDOCTORAL TRAINING IN GENETICS AND REGULATIONT32GM007197 · NIGMS · UNIVERSITY OF CHICAGO · PI ROTHMAN-DENES, LUCIA B. B · 1985 to 2020
$17.0M
Systems Genetic Analysis of Methamphetamine's Motivational Effects in a Mouse AILR01DA021336 · NIDA · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2006 to 2015
$4.0M
Genome-wide association studies in outbred miceR01GM097737 · NIGMS · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2011 to 2014
$1.9M
FINDING GENES THAT CAUSE QLT FOR FEAR LEARNING AND ANXIETYR01MH079103 · NIMH · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2007 to 2011
$1.9M
Mechanisms for 5-HTT control of PPI and perseverative behavior using mouse modelsR01MH079424 · NIMH · UNIVERSITY OF CHICAGO · PI DULAWA, STEPHANIE C · 2007 to 2011
$1.8M
Generation and in vivo validation of cis-regulatory maps in eukaryotic genomesR01HG004428 · NHGRI · UNIVERSITY OF CHICAGO · PI NOBREGA, MARCELO A. · 2007 to 2009
$1.5M
Dissecting of the Tbx20 Regulatory NetworkR01HL088393 · NHLBI · UNIVERSITY OF CHICAGO · PI NOBREGA, MARCELO A. · 2009 to 2010
$844k
In vivo reagents to identify functional noncoding sequences in the TCF7L2 locusR21DK078871 · NIDDK · UNIVERSITY OF CHICAGO · PI NOBREGA, MARCELO A. · 2007 to 2008
$417k
NHGRI NIH HHS HG004428NHGRI NIH HHS R01 HG004428NHLBI NIH HHS R01 HL088393NIDA NIH HHS DA021336NIDA NIH HHS R01 DA021336NIDDK NIH HHS DK-078871NIDDK NIH HHS R21 DK078871NIGMS NIH HHS GM097737NIGMS NIH HHS R01 GM097737NIGMS NIH HHS T32 GM007197NIGMS NIH HHS T32GM007197NIGMS NIH HHS T32 GM007281NIGMS NIH HHS T32GM07281NIMH NIH HHS MH079103NIMH NIH HHS MH079424NIMH NIH HHS R01 MH079103NIMH NIH HHS R01 MH079424
6 · The paper itself

Abstract

The comorbidity of type 2 diabetes (T2D) with several psychiatric diseases is well established. While environmental factors may partially account for these co-occurrences, common genetic susceptibilities could also be implicated in the confluence of these diseases. In support of shared genetic burdens, TCF7L2, the strongest genetic determinant for T2D risk in the human population, has been recently implicated in schizophrenia (SCZ) risk, suggesting that this may be one of many loci that pleiotropically influence both diseases. To investigate whether Tcf7l2 is involved in behavioral phenotypes in addition to its roles in glucose metabolism, we conducted several behavioral tests in mice with null alleles of Tcf7l2 or overexpressing Tcf7l2. We identified a role for Tcf7l2 in anxiety-like behavior and a dose-dependent effect of Tcf7l2 alleles on fear learning. None of the mutant mice showed differences in prepulse inhibition (PPI), which is a well-established endophenotype for SCZ. These results show that Tcf7l2 alters behavior in mice. Importantly, these differences are observed prior to the onset of detectable glucose metabolism abnormalities. Whether these differences are related to human anxiety-disorders or schizophrenia remains to be determined. These animal models have the potential to elucidate the molecular basis of psychiatric comorbidities in diabetes and should therefore be studied further.

Indexed as

Behavior, AnimalAnimalsAnxietyComorbidityDiabetes Mellitus, Type 2EndophenotypesFearGenetic Predisposition to DiseaseGlucoseMiceSchizophreniaTranscription Factor 7-Like 2 ProteinGlucoseTcf7l2 protein, mouseTranscription Factor 7-Like 2 Protein

Identifiers

PMID22046400
PMCPMC3203170
OpenAlexW1966708242

What OpenQuestion holds

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LicenceCC BY
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.