Evidence map›Paper›PMID 29950405›Full record

ArticleMolecular pharmacology2018

A Novel CRISPR/Cas9-Based Cellular Model to Explore Adenylyl Cyclase and cAMP Signaling.

Monica Soto-Velasquez, Michael P Hayes, Aktan Alpsoy, Emily C Dykhuizen, Val J Watts

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. A molecular mechanism to diversify CaNature communications · 2024
    Article
  8. Article
  9. Article
  10. Inhibition of adenylyl cyclase by GTPase-deficient GαCell communication and signaling : CCS · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Adenylyl cyclase 3 regulates osteocyte mechanotransduction and primary cilium.Biochemical and biophysical research communications · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

5 authors at 1 institution in 1 country.

Monica Soto-VelasquezDepartment of Medicinal Chemistry and Molecular Pharmacology (M.S.-V., M.P.H., A.A., E.C.D., V.J.W.), Purdue Institute of Drug Discovery (E.C.D., V.J.W.), Purdue University, West Lafayette, Indiana.
Michael P HayesDepartment of Medicinal Chemistry and Molecular Pharmacology (M.S.-V., M.P.H., A.A., E.C.D., V.J.W.), Purdue Institute of Drug Discovery (E.C.D., V.J.W.), Purdue University, West Lafayette, Indiana.
Aktan AlpsoyDepartment of Medicinal Chemistry and Molecular Pharmacology (M.S.-V., M.P.H., A.A., E.C.D., V.J.W.), Purdue Institute of Drug Discovery (E.C.D., V.J.W.), Purdue University, West Lafayette, Indiana.
Emily C DykhuizenDepartment of Medicinal Chemistry and Molecular Pharmacology (M.S.-V., M.P.H., A.A., E.C.D., V.J.W.), Purdue Institute of Drug Discovery (E.C.D., V.J.W.), Purdue University, West Lafayette, Indiana.
Val J WattsDepartment of Medicinal Chemistry and Molecular Pharmacology (M.S.-V., M.P.H., A.A., E.C.D., V.J.W.), Purdue Institute of Drug Discovery (E.C.D., V.J.W.), Purdue University, West Lafayette, Indiana wattsv@purdue.edu.
Purdue University West Lafayette · US

Funding

Understanding adaptive signaling of neuronal adenyly cyclases using siRNAR33MH101673 · NIMH · PURDUE UNIVERSITY · PI WATTS, VAL J · 2015 to 2016
$889k
Understanding adaptive signaling of neuronal adenyly cyclases using siRNAR21MH101673 · NIMH · PURDUE UNIVERSITY · PI WATTS, VAL J · 2014 to 2014
$261k
NIMH NIH HHS R21 MH101673NIMH NIH HHS R33 MH101673
6 · The paper itself

Abstract

Functional characterization of adenylyl cyclase (AC) isoforms has proven challenging in mammalian cells because of the endogenous expression of multiple AC isoforms and the high background cAMP levels induced by nonselective AC activators. To simplify the characterization of individual transmembrane AC (mAC) isoforms, we generated a human embryonic kidney cell line 293 (HEK293) with low cAMP levels by knocking out two highly expressed ACs, AC3 and AC6, using CRISPR/Cas9 technology. Stable HEK293 cell lines lacking either AC6 (HEK-ACΔ6) or both AC3 and AC6 (HEK-ACΔ3/6) were generated. Knockout was confirmed genetically and by comparing cAMP responses of the knockout cells to the parental cell line. HEK-ACΔ6 and HEK-ACΔ3/6 cells revealed an 85% and 95% reduction in the forskolin-stimulated cAMP response, respectively. Forskolin- and G

Indexed as

Adenylyl CyclasesBinding SitesColforsinCRISPR-Associated Protein 9CRISPR-Cas SystemsCyclic AMPDose-Response Relationship, DrugHEK293 CellsHumansIsoproterenolProtein Structure, SecondarySignal TransductionAdenylyl CyclasesColforsinCRISPR-Associated Protein 9Cyclic AMPIsoproterenol

Identifiers

PMID29950405
PMCPMC6064782
OpenAlexW2811161567

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.