Evidence map›Paper›PMID 19679071›Full record

ArticleNeuron2009

Linking genetically defined neurons to behavior through a broadly applicable silencing allele.

Jun Chul Kim, Melloni N Cook, Megan R Carey, Chung Shen, Wade G Regehr, Susan M Dymecki

Abstract read
In one paragraph

Article in Neuron, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
–field-weighted citation impact
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

96 citing papers in PubMed.

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  14. Diverse roles of pontine NPS-expressing neurons in sleep regulation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Article
  16. Article
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  19. Review
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36 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

6 authors.

Jun Chul KimDepartment of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Melloni N Cook
Megan R Carey
Chung Shen
Wade G Regehr
Susan M Dymecki

Funding

VENTRAL MEDULLA, BREATHING, AND CENTRAL CHEMORECEPTIONP01HD036379 · NICHD · HARVARD MEDICAL SCHOOL · PI DYMECKI, SUSAN M. · 1998 to 2017
$32.2M
Short-Term Synaptic Plasticity in the CNSR37NS032405 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI REGEHR, WADE G · 2005 to 2011
$4.7M
Gene to Phenotype Networks for Alcohol & Drug AddictionR01DA020677 · NIDA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GOLDOWITZ, DANIEL · 2006 to 2008
$2.2M
Mapping neuronal circuits in mice with high selectivityR01DK067826 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI DYMECKI, SUSAN M. · 2004 to 2007
$1.7M
Novel tools to study circuit function, development, and periods of vulnerabilityR21MH083613 · NIMH · HARVARD MEDICAL SCHOOL · PI DYMECKI, SUSAN M. · 2008 to 2009
$709k
Developmental Genetics of Serotonin Neuron Subtypes in Brain Reward CircuitsR21DA023643 · NIDA · HARVARD MEDICAL SCHOOL · PI DYMECKI, SUSAN M. · 2007 to 2010
$707k
NICHD NIH HHS P01 HD036379NIDA NIH HHS R01 DA020677NIDA NIH HHS R21 DA023643NIDDK NIH HHS R01 DK067826NIMH NIH HHS R21 MH083613NIMH NIH HHS R21 MH083613-01NINDS NIH HHS R37 NS032405
6 · The paper itself

Abstract

Tools for suppressing synaptic transmission gain power when able to target highly selective neuron subtypes, thereby sharpening attainable links between neuron type, behavior, and disease; and when able to silence most any neuron subtype, thereby offering broad applicability. Here, we present such a tool, RC::PFtox, that harnesses breadth in scope along with high cell-type selection via combinatorial gene expression to deliver tetanus toxin light chain (tox), an inhibitor of vesicular neurotransmission. When applied in mice, we observed cell-type-specific disruption of vesicle exocytosis accompanied by loss of excitatory postsynaptic currents and commensurately perturbed behaviors. Among various test populations, we applied RC::PFtox to silence serotonergic neurons, en masse or a subset defined combinatorially. Of the behavioral phenotypes observed upon en masse serotonergic silencing, only one mapped to the combinatorially defined subset. These findings provide evidence for separability by genetic lineage of serotonin-modulated behaviors; collectively, these findings demonstrate broad utility of RC::PFtox for dissecting neuron functions.

Indexed as

Acoustic StimulationAnalysis of VarianceAnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsBehavior, AnimalBiophysicsCerebellumConditioning, PsychologicalElectric StimulationExploratory BehaviorFearGABA AntagonistsGenetic LinkageGreen Fluorescent ProteinsIn Vitro TechniquesAtoh1 protein, mouseBasic Helix-Loop-Helix ProteinsCGP 55845AGABA AntagonistsGreen Fluorescent ProteinsGt(ROSA)26Sor non-coding RNA, mouseNerve Tissue ProteinsPhosphinic AcidsPropanolaminesProteinsRecombinasesRNA, UntranslatedSerotoninTetanus ToxinVesicle-Associated Membrane Protein 2

Identifiers

PMID19679071
PMCPMC2814245

What OpenQuestion holds

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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.