Evidence map›Paper›PMID 19694817›Full record

ArticleGenes, brain, and behavior2009

Genomic survey of prepulse inhibition in mouse chromosome substitution strains.

M P Leussis, M L Frayne, M Saito, E M Berry, K A Aldinger, G N Rockwell, R P Hammer, A E Baskin-Hill, J B Singer, J H Nadeau and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Genes, brain, and behavior, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Forward genetic approaches to understanding complex behaviors.Current topics in behavioral neurosciences · 2012
    Review
  5. Article
  6. Review
  7. Article
  8. 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

12 authors at 7 institutions in 1 country.

M P LeussisPsychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA, USA.
M L Frayne
M Saito
E M Berry
K A Aldinger
G N Rockwell
R P Hammer
A E Baskin-Hill
J B Singer
J H Nadeau
P Sklar
T L Petryshen
Massachusetts Institute of Technology · USCase Western Reserve University · USMassachusetts General Hospital · USBroad Institute · USHarvard University · USNovartis (United States) · USUniversity of Arizona · US

Funding

MOUSE GENETIC RESOURCES FOR MULTIGENIC DISEASE ANALYSIS: AIDSP40RR012305 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI BERGER, NATHAN A. · 1996 to 2011
$6.8M
Haplotype and Expression Mapping of Prepulse InhibitionR21MH071673 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI SKLAR, PAMELA · 2005 to 2006
$375k
CIHRNCRR NIH HHS P40 RR012305NCRR NIH HHS RR12305NIMH NIH HHS R01 MH0703930NIMH NIH HHS R21 MH071673
6 · The paper itself

Abstract

Prepulse inhibition (PPI) is a measure of sensorimotor gating, a pre-attentional inhibitory brain mechanism that filters extraneous stimuli. Prepulse inhibition is correlated with measures of cognition and executive functioning, and is considered an endophenotype of schizophrenia and other psychiatric illnesses in which patients show PPI impairments. As a first step toward identifying genes that regulate PPI, we performed a quantitative trait locus (QTL) screen of PPI phenotypes in a panel of mouse chromosome substitution strains (CSSs). We identified five CSSs with altered PPI compared with the host C57BL/6J strain: CSS-4 exhibited decreased PPI, whereas CSS-10, -11, -16 and -Y exhibited higher PPI compared with C57BL/6J. These data indicate that A/J chromosomes 4, 10, 11, 16 and Y harbor at least one QTL region that modulates PPI in these CSSs. Quantitative trait loci for the acoustic startle response were identified on seven chromosomes. Like PPI, habituation of the startle response is also disrupted in schizophrenia, and in the present study CSS-7 and -8 exhibited deficits in startle habituation. Linkage analysis of an F(2) intercross identified a highly significant QTL for PPI on chromosome 11 between positions 101.5 and 114.4 Mb (peak LOD = 4.54). Future studies will map the specific genes contributing to these QTLs using congenic strains and other genomic approaches. Identification of genes that modulate PPI will provide insight into the neural mechanisms underlying sensorimotor gating, as well as the psychopathology of disorders characterized by gating deficits.

Indexed as

GenomeAnimalsBrain ChemistryChromosome MappingChromosomes, MammalianCrosses, GeneticFemaleGenetic Predisposition to DiseaseGenetic VariationGenotypeHabituation, PsychophysiologicMaleMiceMice, Inbred C57BLMice, Mutant StrainsMice, Neurologic Mutants

Identifiers

PMID19694817
PMCPMC3746005
OpenAlexW2014669938

What OpenQuestion holds

Textmetadata
LicenceTDM
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.