Evidence map›Paper›PMID 20647312›Full record

ArticleThe Journal of biological chemistry2010

Acylation-dependent export of Trypanosoma cruzi phosphoinositide-specific phospholipase C to the outer surface of amastigotes.

Vicente de Paulo Martins, Michael Okura, Danijela Maric, David M Engman, Mauricio Vieira, Roberto Docampo, Silvia N J Moreno

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Calcium signaling in intracellular protist parasites.Current opinion in microbiology · 2021
    Review
  6. Article
  7. The IPBiochimica et biophysica acta. Molecular cell research · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Intracellular calcium channels in protozoa.European journal of pharmacology · 2014
    Review
  20. Review
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

7 authors at 3 institutions in 1 country.

Vicente de Paulo MartinsDepartment of Cellular Biology, University of Georgia, Center for Tropical and Emerging Global Diseases, Athens, Georgia 30602, USA.
Michael Okura
Danijela Maric
David M Engman
Mauricio Vieira
Roberto Docampo
Silvia N J Moreno
University of Georgia · USNorthwestern University · USUniversity of Illinois Urbana-Champaign · US

Funding

Structure and Function of the Trypanosome Flagellar MembraneR01GM093359 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ENGMAN, DAVID M. · 2010 to 2013
$1.2M
Novel phospholipases C in trypanosomatidsR01AI058297 · NIAID · UNIVERSITY OF GEORGIA · PI MORENO, SILVIA N · 2006 to 2009
$1.1M
NIAID NIH HHS AI-058297NIAID NIH HHS R01 AI058297NIGMS NIH HHS R01 GM093359
6 · The paper itself

Abstract

Phosphoinositide phospholipase C (PI-PLC) plays an essential role in cell signaling. A unique Trypanosoma cruzi PI-PLC (TcPI-PLC) is lipid-modified in its N terminus and localizes to the plasma membrane of amastigotes. Here, we show that TcPI-PLC is located onto the extracellular phase of the plasma membrane of amastigotes and that its N-terminal 20 amino acids are necessary and sufficient to target the fused GFP to the outer surface of the parasite. Mutagenesis of the predicted acylated residues confirmed that myristoylation of a glycine residue in the 2nd position and acyl modification of a cysteine in the 4th but not in the 8th or 15th position of the coding sequence are required for correct plasma membrane localization in T. cruzi epimastigotes or amastigotes. Interestingly, mutagenesis of the cysteine at the 8th position increased its flagellar localization. When expressed as fusion constructs with GFP, the N-terminal 6 and 10 amino acids fused to GFP are predominantly located in the cytosol and concentrated in a compartment that co-localizes with a Golgi complex marker. The N-terminal 20 amino acids of TcPI-PLC associate with lipid rafts when dually acylated. Taken together, these results indicate that N-terminal acyl modifications serve as a molecular addressing system for sending TcPI-PLC to the outer surface of the cell.

Indexed as

AcylationAnimalsCell LineCytosolGolgi ApparatusMembrane MicrodomainsMutagenesisPhosphoinositide Phospholipase CProtein Processing, Post-TranslationalProtein TransportProtozoan ProteinsTrypanosoma cruziPhosphoinositide Phospholipase CProtozoan Proteins

Identifiers

PMID20647312
PMCPMC2945582
OpenAlexW2023847294

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.