Evidence map›Paper›PMID 21343290›Full record

ArticleThe Journal of biological chemistry2011

Gi/o signaling and the palmitoyltransferase DHHC2 regulate palmitate cycling and shuttling of RGS7 family-binding protein.

Lixia Jia, Maurine E Linder, Kendall J Blumer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. 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
1.9field-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, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Mechanisms and Regulation of Neuronal GABACurrent topics in behavioral neurosciences · 2022
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. How many lives does CLIMP-63 have?Biochemical Society transactions · 2015
    Review
  12. The physiology of protein S-acylation.Physiological reviews · 2015
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. GIRK channel modulation by assembly with allosterically regulated RGS proteins.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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

3 authors at 2 institutions in 1 country.

Lixia JiaDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Maurine E Linder
Kendall J Blumer
Washington University in St. Louis · USCornell University · US

Funding

MECHANISM &REGULATION OF RECEPTOR G PROTEIN SIGNALINGR01GM044592 · NIGMS · WASHINGTON UNIVERSITY · PI BLUMER, KENDALL J · 1990 to 2017
$7.5M
RGS PROTEIN FUNCTION AND REGULATIONR01HL075632 · NHLBI · WASHINGTON UNIVERSITY · PI BLUMER, KENDALL J · 2005 to 2013
$4.5M
PROTEIN PALMITOYLATION IN SIGNALING SYSTEMSR01GM051466 · NIGMS · WASHINGTON UNIVERSITY · PI LINDER, MAURINE E · 1994 to 2010
$3.2M
NHLBI NIH HHS HL075632NHLBI NIH HHS R01 HL075632NIGMS NIH HHS GM044592NIGMS NIH HHS GM051466NIGMS NIH HHS R01 GM044592NIGMS NIH HHS R01 GM051466
6 · The paper itself

Abstract

R7BP (RGS7 family-binding protein) has been proposed to function in neurons as a palmitoylation-regulated protein that shuttles heterodimeric, G(i/o)α-specific GTPase-activating protein (GAP) complexes composed of Gβ5 and RGS7 (R7) isoforms between the plasma membrane and nucleus. To test this hypothesis we studied R7BP palmitoylation and localization in neuronal cells. We report that R7BP undergoes dynamic, signal-regulated palmitate turnover; the palmitoyltransferase DHHC2 mediates de novo and turnover palmitoylation of R7BP; DHHC2 silencing redistributes R7BP from the plasma membrane to the nucleus; and G(i/o) signaling inhibits R7BP depalmitoylation whereas G(i/o) inactivation induces nuclear accumulation of R7BP. In concert with previous evidence, our findings suggest that agonist-induced changes in palmitoylation state facilitate GAP action by (i) promoting Giα depalmitoylation to create optimal GAP substrates, and (ii) inhibiting R7BP depalmitoylation to stabilize membrane association of R7-Gβ5 GAP complexes. Regulated palmitate turnover may also enable R7BP-bound GAPs to shuttle between sites of low and high G(i/o) activity or the plasma membrane and nucleus, potentially providing spatio-temporal control of signaling by G(i/o)-coupled receptors.

Indexed as

Active Transport, Cell NucleusAcyltransferasesAnimalsCarrier ProteinsCell NucleusGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding Protein beta SubunitsHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsLipoylationPalmitic AcidProtein Processing, Post-TranslationalRatsRats, Sprague-DawleyRGS ProteinsAcyltransferasesCarrier ProteinsGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding Protein beta SubunitsIntracellular Signaling Peptides and ProteinsPalmitic AcidRGS7BP protein, humanRGS ProteinsTumor Suppressor ProteinsZDHHC2 protein, human

Identifiers

PMID21343290
PMCPMC3075713
OpenAlexW2033785292

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.