Evidence map›Paper›PMID 28768828›Full record

ArticleMolecular biology of the cell2017

Sphingolipids facilitate age asymmetry of membrane proteins in dividing yeast cells.

Pushpendra Singh, Sree Kumar Ramachandran, Jin Zhu, Byoung Choul Kim, Debojyoti Biswas, Taekjip Ha, Pablo A Iglesias, Rong Li

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Cell membrane asymmetries and cellular aging.The Biochemical journal · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Membrane Heterogeneity Beyond the Plasma Membrane.Frontiers in cell and developmental biology · 2020
    Review
  11. Article
  12. Article
  13. Distinct segregation patterns of yeast cell-peripheral proteins uncovered by a method for protein segregatome analysis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  14. 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

8 authors at 2 institutions in 2 countries.

Pushpendra SinghCenter for Cell Dynamics, Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Sree Kumar RamachandranCenter for Cell Dynamics, Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Jin ZhuCenter for Cell Dynamics, Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Byoung Choul KimDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University, Baltimore, MD 21205.
Debojyoti BiswasElectrical and Computer Engineering, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21218.
Taekjip HaDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University, Baltimore, MD 21205.
Pablo A IglesiasCenter for Cell Dynamics, Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Rong LiCenter for Cell Dynamics, Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205 rong@jhu.edu.
Johns Hopkins University · USHoward Hughes Medical Institute · US

Funding

Cellular dynamics in division, motility and evolutionary adaptationR35GM118172 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LI, RONG · 2016 to 2019
$2.8M
NIGMS NIH HHS R35 GM118172
6 · The paper itself

Abstract

One proposed mechanism of cellular aging is the gradual loss of certain cellular components that are insufficiently renewed. In an earlier study, multidrug resistance transporters (MDRs) were postulated to be such aging determinants during the yeast replicative life span (RLS). Aged MDR proteins were asymmetrically retained by the aging mother cell and did not diffuse freely into the bud, whereas newly synthesized MDR proteins were thought to be deposited mostly in the bud before cytokinesis. In this study, we further demonstrate the proposed age asymmetry of MDR proteins in dividing yeast cells and investigate the mechanism that controls diffusive properties of MDR proteins to maintain this asymmetry. We found that long-chain sphingolipids, but not the septin/endoplasmic reticulum-based membrane diffusion barrier, are important for restricting MDR diffusion. Depletion of sphingolipids or shortening of their long acyl chains resulted in an increase in the lateral mobility of MDR proteins, causing aged MDR protein in the mother cell to enter the bud. We used a mathematical model to understand the effect of diminished MDR age asymmetry on yeast cell aging, the result of which was qualitatively consistent with the observed RLS shortening in sphingolipid mutants.

Indexed as

AntiportersATP Binding Cassette Transporter, Subfamily BCell DivisionCytokinesisDNA ReplicationEndoplasmic ReticulumMembrane ProteinsMembrane Transport ProteinsOrganic Cation Transport ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSphingolipidsAntiportersATP Binding Cassette Transporter, Subfamily BMembrane ProteinsMembrane Transport ProteinsOrganic Cation Transport ProteinsSaccharomyces cerevisiae ProteinsSphingolipidsTPO1 protein, S cerevisiae

Identifiers

PMID28768828
PMCPMC5620378
OpenAlexW2741077110

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.