Evidence map›Paper›PMID 19403696›Full record

ArticleMolecular biology of the cell2009

Control of protein and sterol trafficking by antagonistic activities of a type IV P-type ATPase and oxysterol binding protein homologue.

Baby-Periyanayaki Muthusamy, Sumana Raychaudhuri, Paramasivam Natarajan, Fumiyoshi Abe, Ke Liu, William A Prinz, Todd R Graham

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Regulation of yeast polarized exocytosis by phosphoinositide lipids.Cellular and molecular life sciences : CMLS · 2024
    Review
  2. Review
  3. Article
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  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Insights into the mechanisms of sterol transport between organelles.Cellular and molecular life sciences : CMLS · 2013
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. A detour for yeast oxysterol binding proteins.The Journal of biological chemistry · 2012
    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

7 authors at 3 institutions in 2 countries.

Baby-Periyanayaki MuthusamyDepartment of Biological Sciences, Vanderbilt University, Nashville, TN 37235-1634, USA.
Sumana Raychaudhuri
Paramasivam Natarajan
Fumiyoshi Abe
Ke Liu
William A Prinz
Todd R Graham
Vanderbilt University · USNational Institutes of Health · USJapan Agency for Marine-Earth Science and Technology · JP

Funding

Intracellular Lipid Trafficking and Organelle BiogenesisZIADK060004 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI PRINZ, WILLIAM · 2009 to 2022
$8.5M
Drs2p Function in Clathrin-coated Vesicle BuddingR01GM062367 · NIGMS · VANDERBILT UNIVERSITY · PI GRAHAM, TODD R · 2001 to 2013
$3.4M
Intramural NIH HHSNIGMS NIH HHS GM-62367NIGMS NIH HHS R01 GM062367
6 · The paper itself

Abstract

The oxysterol binding protein homologue Kes1p has been implicated in nonvesicular sterol transport in Saccharomyces cerevisiae. Kes1p also represses formation of protein transport vesicles from the trans-Golgi network (TGN) through an unknown mechanism. Here, we show that potential phospholipid translocases in the Drs2/Dnf family (type IV P-type ATPases [P4-ATPases]) are downstream targets of Kes1p repression. Disruption of KES1 suppresses the cold-sensitive (cs) growth defect of drs2Delta, which correlates with an enhanced ability of Dnf P4-ATPases to functionally substitute for Drs2p. Loss of Kes1p also suppresses a drs2-ts allele in a strain deficient for Dnf P4-ATPases, suggesting that Kes1p antagonizes Drs2p activity in vivo. Indeed, Drs2-dependent phosphatidylserine translocase (flippase) activity is hyperactive in TGN membranes from kes1Delta cells and is potently attenuated by addition of recombinant Kes1p. Surprisingly, Drs2p also antagonizes Kes1p activity in vivo. Drs2p deficiency causes a markedly increased rate of cholesterol transport from the plasma membrane to the endoplasmic reticulum (ER) and redistribution of endogenous ergosterol to intracellular membranes, phenotypes that are Kes1p dependent. These data suggest a homeostatic feedback mechanism in which appropriately regulated flippase activity in the Golgi complex helps establish a plasma membrane phospholipid organization that resists sterol extraction by a sterol binding protein.

Indexed as

Sequence Homology, Amino AcidCalcium-Transporting ATPasesCell MembraneCloning, MolecularCold TemperatureEndosomesGenes, FungalGenetic Complementation TestMembrane ProteinsMutationOxysterol Binding ProteinsPhenotypeProtein TransportReceptors, SteroidSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCalcium-Transporting ATPasesDRS2 protein, S cerevisiaeKES1 protein, S cerevisiaeMembrane ProteinsOxysterol Binding ProteinsReceptors, SteroidSaccharomyces cerevisiae ProteinsSterols

Identifiers

PMID19403696
PMCPMC2695799
OpenAlexW2154499074

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.