Evidence map›Paper›PMID 22562055›Full record

ReviewBiochimica et biophysica acta2012

Regulation of the Golgi complex by phospholipid remodeling enzymes.

Kevin D Ha, Benjamin A Clarke, William J Brown

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Cytosolic Phospholipase AMolecular neurobiology · 2019
    Article
  6. Review
  7. Phospholipid subcellular localization and dynamics.The Journal of biological chemistry · 2018
    Review
  8. Article
  9. Article
  10. Golgi apparatus self-organizes into the characteristic shape via postmitotic reassembly dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. ER trapping reveals Golgi enzymes continually revisit the ER through a recycling pathway that controls Golgi organization.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  16. Review
  17. Review
  18. Factors influencing the eicosanoids synthesis in vivo.BioMed research international · 2015
    Review
  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 1 institution in 1 country.

Kevin D HaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Benjamin A Clarke
William J Brown
Cornell University · US

Funding

MEMBRANE TRAFFICKING IN MAMMALIAN CELLSR01DK051596 · NIDDK · CORNELL UNIVERSITY ITHACA · PI BROWN, WILLIAM J · 1996 to 2009
$3.0M
Role of Phospholipid Remodeling in Secretion and Golgi Function in Mammalian CellR01GM101027 · NIGMS · CORNELL UNIVERSITY · PI BROWN, WILLIAM J · 2013 to 2016
$1.2M
NIDDK NIH HHS R01 DK051596NIGMS NIH HHS R01 GM101027PHS HHS R01 51596
6 · The paper itself

Abstract

The mammalian Golgi complex is a highly dynamic organelle consisting of stacks of flattened cisternae with associated coated vesicles and membrane tubules that contribute to cargo import and export, intra-cisternal trafficking, and overall Golgi architecture. At the morphological level, all of these structures are continuously remodeled to carry out these trafficking functions. Recent advances have shown that continual phospholipid remodeling by phospholipase A (PLA) and lysophospholipid acyltransferase (LPAT) enzymes, which deacylate and reacylate Golgi phospholipids, respectively, contributes to this morphological remodeling. Here we review the identification and characterization of four cytoplasmic PLA enzymes and one integral membrane LPAT that participate in the dynamic functional organization of the Golgi complex, and how some of these enzymes are integrated to determine the relative abundance of COPI vesicle and membrane tubule formation. This article is part of a Special Issue entitled Lipids and Vesicular Transport.

Indexed as

1-Acylglycerophosphocholine O-AcyltransferaseAnimalsCOP-Coated VesiclesGene ExpressionGolgi ApparatusHumansIsoenzymesLipid MetabolismMembrane MicrodomainsMembrane ProteinsPhospholipases APhospholipidsProtein TransportSaccharomyces cerevisiae1-Acylglycerophosphocholine O-AcyltransferaseIsoenzymesMembrane ProteinsPhospholipases APhospholipids

Identifiers

PMID22562055
PMCPMC3399269
OpenAlexW2141208045

What OpenQuestion holds

Textmetadata
LicenceTDM
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.