Evidence map›Paper›PMID 12397184›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Orphan G protein-coupled receptors MrgA1 and MrgC11 are distinctively activated by RF-amide-related peptides through the Galpha q/11 pathway.

Sang-Kyou Han, Xinzhong Dong, Jong-Ik Hwang, Mark J Zylka, David J Anderson, Melvin I Simon

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

71 citing papers in PubMed, 164 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. MRGPRX4 in Cholestatic Pruritus.Seminars in liver disease · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Potential and Realized Impact of Astroglia CaFrontiers in cellular neuroscience · 2021
    Review
  15. Review
  16. Complementary roles of murine NaScientific reports · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. Conopeptides promote itch through human itch receptor hMgprX1.Toxicon : official journal of the International Society on Toxinology · 2018
    Article

11 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 at 2 institutions in 1 country.

Sang-Kyou HanDivision of Biology 147-75, California Institute of Technology, Pasadena 91125, USA.
Xinzhong Dong
Jong-Ik Hwang
Mark J Zylka
David J Anderson
Melvin I Simon
Howard Hughes Medical Institute · USCalifornia Institute of Technology · US

Funding

MOLECULAR BASIS OF SIGNAL TRANSDUCTIONR37GM034236 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI SIMON, MELVIN · 1997 to 2006
$2.9M
MOLECULAR BASIS OF SIGNAL TRANSDUCTIONR01GM034236 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI SIMON, MELVIN · 1985 to 1996
–
NIGMS NIH HHS GM-34236NIGMS NIH HHS R37 GM034236
6 · The paper itself

Abstract

MrgA1 and MrgC11 belong to a recently identified family of orphan G-protein coupled receptors, called mrgs (mas-related genes). They are only expressed in a specific subset of sensory neurons that are known to detect painful stimuli. However, the precise physiological function of Mrg receptors and their underlying mechanisms of signal transduction are not known. We therefore have screened a series of neuropeptides against human embryonic kidney (HEK) 293 cells that stably express either MrgA1 or MrgC11 to identify ligands and/or agonists. MrgA1- or MrgC11-specific agonists stimulated dose-dependent increases in intracellular free Ca(2+) in a pertussis toxin-insensitive manner, but failed to alter basal or forskolin-stimulated levels of intracellular cAMP. Furthermore, studies using embryonic fibroblasts derived from various Galpha protein knockout mice demonstrated that both the MrgA1 and MrgC11 receptors are coupled to the Galpha(q/11) signaling pathway. Screening of neuropeptides identified surrogate agonists, most of these peptides included a common C-terminal -RF(Y)G or -RF(Y) amide motif. Structure-function studies suggest that endogenous ligands of Mrg receptors are likely to be RF(Y)G and/or RF(Y) amide-related peptides and that postprocessing of these peptides may serve to determine Mrg receptor-ligand specificity. The differences in ligand specificity also suggest functional diversity amongst the Mrg receptors.

Indexed as

Receptors, G-Protein-CoupledAmino Acid SequenceAnimalsCalcium SignalingCell LineCyclic AMPFibroblastsGTP-Binding Protein alpha Subunits, Gq-G11GTP-Binding ProteinsHeterotrimeric GTP-Binding ProteinsHumansMiceMice, KnockoutMolecular Sequence DataReceptors, Cell SurfaceRecombinant ProteinsCyclic AMPGTP-Binding Protein alpha Subunits, Gq-G11GTP-Binding ProteinsHeterotrimeric GTP-Binding ProteinsMrgA1 protein, mouseMrgprx1 protein, mouseReceptors, Cell SurfaceReceptors, G-Protein-CoupledRecombinant Proteins

Identifiers

PMID12397184
PMCPMC137489
OpenAlexW2090905251

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.