Evidence map›Paper›PMID 25255106›Full record

ArticlePLoS genetics2014

Requirement for Drosophila SNMP1 for rapid activation and termination of pheromone-induced activity.

Zhengzheng Li, Jinfei D Ni, Jia Huang, Craig Montell

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

48 citing papers in PubMed, 131 citations in OpenAlex.

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  6. Targeted deletion of olfactory receptors inJournal of neurogenetics · 2024
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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

4 authors at 3 institutions in 1 country.

Zhengzheng LiDepartment of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Jinfei D NiDepartment of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Neuroscience Research Institute and Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, Santa Barbara, California.
Jia HuangNeuroscience Research Institute and Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, Santa Barbara, California.
Craig MontellNeuroscience Research Institute and Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, Santa Barbara, California.
University of California, Santa Barbara · USJohns Hopkins Medicine · USJohns Hopkins University · US

Funding

Molecular Genetics of Taste TransductionR01DC007864 · NIDCD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI CRAIG MONTELL · 2006 to 2026
$7.5M
TRPA1: a polymodal sensor for aversive stimuliR01GM085335 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI MONTELL, CRAIG · 2008 to 2015
$2.8M
NIDCD NIH HHS DC007864NIDCD NIH HHS R01 DC007864NIGMS NIH HHS GM085335NIGMS NIH HHS R01 GM085335
6 · The paper itself

Abstract

Pheromones are used for conspecific communication by many animals. In Drosophila, the volatile male-specific pheromone 11-cis vaccenyl acetate (cVA) supplies an important signal for gender recognition. Sensing of cVA by the olfactory system depends on multiple components, including an olfactory receptor (OR67d), the co-receptor ORCO, and an odorant binding protein (LUSH). In addition, a CD36 related protein, sensory neuron membrane protein 1 (SNMP1) is also involved in cVA detection. Loss of SNMP1 has been reported to eliminate cVA responsiveness, and to greatly increase spontaneous activity of OR67d-expressing olfactory receptor neurons (ORNs). Here, we found the snmp1(1) mutation did not abolish cVA responsiveness or cause high spontaneous activity. The cVA responses in snmp1 mutants displayed a delayed onset, and took longer to reach peak activity than wild-type. Most strikingly, loss of SNMP1 caused a dramatic delay in signal termination. The profound impairment in signal inactivation accounted for the previously reported "spontaneous activity," which represented continuous activation following transient exposure to environmental cVA. We introduced the silk moth receptor (BmOR1) in OR67d ORNs of snmp1(1) flies and found that the ORNs showed slow activation and deactivation kinetics in response to the BmOR1 ligand (bombykol). We expressed the bombykol receptor complex in Xenopus oocytes in the presence or absence of the silk moth SNMP1 (BmSNMP) and found that addition of BmSNMP accelerated receptor activation and deactivation. Our results thus clarify SNMP1 as an important player required for the rapid kinetics of the pheromone response in insects.

Indexed as

Action PotentialsAnimalsBehavior, AnimalDrosophilaFemaleMaleMembrane ProteinsMutationNerve Tissue ProteinsOleic AcidsOlfactory Receptor NeuronsPheromones11-cis-vaccenyl acetateMembrane ProteinsNerve Tissue ProteinsOleic AcidsPheromonessensory neuron membrane protein 1

Identifiers

PMID25255106
PMCPMC4177743
OpenAlexW2007469595

What OpenQuestion holds

Textmetadata
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.