Evidence map›Paper›PMID 8491183›Full record

ArticleThe EMBO journal1993

Phosphatidylethanolamine is the donor of the terminal phosphoethanolamine group in trypanosome glycosylphosphatidylinositols.

A K Menon, M Eppinger, S Mayor, R T Schwarz

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Genome-wide CRISPR screen reveals CLPTM1L as a lipid scramblase required for efficient glycosylphosphatidylinositol biosynthesis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Frontiers in cellular and infection microbiology · 2021
    Article
  13. Lipid composition of the cancer cell membrane.Journal of bioenergetics and biomembranes · 2020
    Review
  14. Selenoprotein I is essential for murine embryogenesis.Archives of biochemistry and biophysics · 2020
    Article
  15. Article
  16. Review
  17. Review
  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

4 authors at 1 institution in 1 country.

A K MenonLaboratory of Molecular Parasitology, Rockefeller University, New York, NY 10021.
M Eppinger
S Mayor
R T Schwarz
Rockefeller University · US

Funding

STRUCTURE AND PROCESSING OF TRYPANOSOME VARIANT ANTIGENSR01AI021531 · NIAID · ROCKEFELLER UNIVERSITY · PI CROSS, GEORGE ALAN MARTIN · 1985 to 1996
–
BIOSYNTHESIS OF MEMBRANE PROTEIN GLYCOLIPID ANCHORSR01AI028858 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI MENON, ANANT K · 1991 to 1996
–
NIAID NIH HHS AI21531NIAID NIH HHS AI28858
6 · The paper itself

Abstract

A variety of eukaryotic cell surface proteins, including the variant surface glycoproteins of African trypanosomes, rely on a covalently attached lipid, glycosylphosphatidylinositol (GPI), for membrane attachment. GPI anchors are synthesized in the endoplasmic reticulum by stepwise glycosylation of phosphatidylinositol (via UDP-GlcNAc and dolichol-P-mannose) followed by the addition of phosphoethanolamine. The experiments described in this paper are aimed at identifying the biosynthetic origin of the terminal phosphoethanolamine group. We show that trypanosome GPIs can be labelled via CDP-[3H]ethanolamine or [beta-32P]CDP-ethanolamine in a cell-free system, indicating that phosphoethanolamine is acquired en bloc. In pulse-chase experiments with CDP-[3H]ethanolamine we show that the GPI phosphoethanolamine is not derived directly from CDP-ethanolamine, but instead from a relatively stable metabolite, such as phosphatidylethanolamine (PE), generated from CDP-ethanolamine in the cell-free system. To test the possibility that PE is the immediate donor of the GPI phosphoethanolamine moiety, we describe metabolic labelling experiments with [3H]serine and show that GPIs can be labelled in the absence of detectable radiolabelled CDP-ethanolamine, presumably via [3H]PE generated from [3H]phosphatidylserine (PS). The data support the proposal that the terminal phosphoethanolamine group in trypanosome GPIs is derived from PE.

Indexed as

AnimalsCell-Free SystemCytidine DiphosphateEthanolaminesGlycosylphosphatidylinositolsPhosphatidylethanolaminesRatsSerineTrypanosoma brucei bruceiVariant Surface Glycoproteins, TrypanosomaCDP ethanolamineCytidine DiphosphateEthanolaminesGlycosylphosphatidylinositolsPhosphatidylethanolaminesphosphorylethanolamineSerineVariant Surface Glycoproteins, Trypanosoma

Identifiers

PMID8491183
PMCPMC413411
OpenAlexW1891938237

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.