Evidence map›Paper›PMID 24646679›Full record

ArticleGenetics2014

Diverse cell type-specific mechanisms localize G protein-coupled receptors to Caenorhabditis elegans sensory cilia.

Andrea G Brear, Jason Yoon, Martin Wojtyniak, Piali Sengupta

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Functions and trafficking mechanisms of RIC-8 inMolecular biology of the cell · 2026
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  16. TheeLife · 2019
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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 1 institution in 1 country.

Andrea G BrearDepartment of Biology and National Center for Behavioral Genomics, Brandeis University, Waltham, Massachusetts 02454.
Jason YoonDepartment of Biology and National Center for Behavioral Genomics, Brandeis University, Waltham, Massachusetts 02454.
Martin WojtyniakDepartment of Biology and National Center for Behavioral Genomics, Brandeis University, Waltham, Massachusetts 02454.
Piali SenguptaDepartment of Biology and National Center for Behavioral Genomics, Brandeis University, Waltham, Massachusetts 02454 sengupta@brandeis.edu.
Brandeis University · US

Funding

Mouse CoreP30NS045713 · NINDS · BRANDEIS UNIVERSITY · PI ROSBASH, MICHAEL · 2003 to 2013
$7.8M
GENETIC AND BIOCHEMICAL MECHANISMS OF REGULATIONT32GM007122 · NIGMS · BRANDEIS UNIVERSITY · PI LOVETT, SUSAN THOMAS · 1985 to 2020
$7.5M
GENETIC ANALYSIS OF SENSORY SPECIFICATION IN C ELEGANSR01GM056223 · NIGMS · BRANDEIS UNIVERSITY · PI SENGUPTA, PIALI · 1997 to 2009
$3.3M
Genetic analysis of sensory specification in C.elegansR37GM056223 · NIGMS · BRANDEIS UNIVERSITY · PI SENGUPTA, PIALI · 2010 to 2016
$2.6M
NIGMS NIH HHS R01 GM056223NIGMS NIH HHS R37 GM056223NIGMS NIH HHS R37 GM56223NIGMS NIH HHS T32 GM007122NINDS NIH HHS P30 NS045713NINDS NIH HHS P30 NS45713
6 · The paper itself

Abstract

The localization of signaling molecules such as G protein-coupled receptors (GPCRs) to primary cilia is essential for correct signal transduction. Detailed studies over the past decade have begun to elucidate the diverse sequences and trafficking mechanisms that sort and transport GPCRs to the ciliary compartment. However, a systematic analysis of the pathways required for ciliary targeting of multiple GPCRs in different cell types in vivo has not been reported. Here we describe the sequences and proteins required to localize GPCRs to the cilia of the AWB and ASK sensory neuron types in Caenorhabditis elegans. We find that GPCRs expressed in AWB or ASK utilize conserved and novel sequences for ciliary localization, and that the requirement for a ciliary targeting sequence in a given GPCR is different in different neuron types. Consistent with the presence of multiple ciliary targeting sequences, we identify diverse proteins required for ciliary localization of individual GPCRs in AWB and ASK. In particular, we show that the TUB-1 Tubby protein is required for ciliary localization of a subset of GPCRs, implying that defects in GPCR localization may be causal to the metabolic phenotypes of tub-1 mutants. Together, our results describe a remarkable complexity of mechanisms that act in a protein- and cell-specific manner to localize GPCRs to cilia, and suggest that this diversity allows for precise regulation of GPCR-mediated signaling as a function of external and internal context.

Indexed as

Amino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCiliaConserved SequenceMolecular Sequence DataReceptors, G-Protein-CoupledSensory Receptor CellsSignal TransductionCaenorhabditis elegans ProteinsReceptors, G-Protein-CoupledSRBC-64 protein, C eleganstub-1 protein, C elegansC. elegansciliaGPCRtubby

Identifiers

PMID24646679
PMCPMC4063923
OpenAlexW2070305224

What OpenQuestion holds

Textmetadata
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.