Evidence map›Paper›PMID 8663363›Full record

ArticleThe Journal of biological chemistry1996

Cloning and characterization of the signal transduction of four splice variants of the human pituitary adenylate cyclase activating polypeptide receptor. Evidence for dual coupling to adenylate cyclase and phospholipase C.

J R Pisegna, S A Wank

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of biological chemistry, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

65 citing papers in PubMed, 187 citations in OpenAlex.

  1. Article
  2. PACInternational journal of molecular sciences · 2022
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Peptide receptors as cancer drug targets.Annals of the New York Academy of Sciences · 2019
    Review
  14. Article
  15. Review
  16. Review
  17. PAC1 Receptors: Shapeshifters in Motion.Journal of molecular neuroscience : MN · 2019
    Review
  18. Review
  19. PACAP-38 and PACAP(6-38) Degranulate Rat Meningeal Mast CellsFrontiers in cellular neuroscience · 2019
    Article
  20. Review

5 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

2 authors at 1 institution in 1 country.

J R PisegnaDigestive Diseases Branch, National Institute of Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
S A Wank
National Institutes of Health · US

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
BLRD VA I01 BX004560NIDDK NIH HHS P30 DK041301RRD VA I01 RX000194
6 · The paper itself

Abstract

Alternative splicing of two exons of the rat pituitary adenylate cyclase activating polypeptide (PACAP) receptor gene generates four major splice variants that are differentially expressed in specific tissues and variably coupled to intracellular second messengers. To evaluate the potential implications of these findings in human physiology, the human PACAP receptor gene was cloned. Alternative splicing about two exons of the gene allowed for four major splice variants that were subsequently identified on cDNA cloning. Each of the four splice variant cDNAs (null, SV-1, SV-2, and SV-3) was stably expressed in NIH/3T3 cells at similar receptor densities. For each splice variant, PACAP (both PACAP-38 and PACAP-27) had similar affinity and potency for stimulating either adenylate cyclase or phospholipase C. However, each receptor splice variant differed in their ligand-stimulated maximal response (efficacy) for total inositol phosphate accumulation with the SV-2 showing the greatest efficacy, followed by the null, SV-1, and SV-3 splice variants. Therefore, unlike the rat, PACAP binds and stimulates signal transduction with nearly equal affinity and potency for each of the receptor splice variants although with varying efficacy for the stimulation of phospholipase C. These results suggest a novel and potentially important mechanism for a single hormone to not only couple to dual signal transduction cascades but also elicit tissue-specific differential activation of phospholipase C in humans.

Indexed as

Alternative SplicingGenetic VariationSignal Transduction3T3 CellsAdenylyl CyclasesAmino Acid SequenceAnimalsBase SequenceCloning, MolecularDNA PrimersExonsHumansInositol PhosphatesKineticsMiceMolecular Sequence DataADCYAP1 protein, humanAdcyap1 protein, mouseAdcyap1 protein, ratADCYAP1R1 protein, humanAdenylyl CyclasesDNA PrimersInositol PhosphatesNeuropeptidesNeurotransmitter AgentsPituitary Adenylate Cyclase-Activating PolypeptideReceptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type IRecombinant ProteinsType C Phospholipases

Identifiers

PMID8663363
PMCPMC6721843
OpenAlexW2057431321

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.