Evidence map›Paper›PMID 32461215›Full record

ArticleLife science alliance2020

Lipid-associated PML structures assemble nuclear lipid droplets containing CCTα and Lipin1.

Jonghwa Lee, Jayme Salsman, Jason Foster, Graham Dellaire, Neale D Ridgway

Abstract read
In one paragraph

Article in Life science alliance, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Inner Nuclear Membrane Has a Unique Lipid Signature.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  6. Article
  7. Review
  8. Mechanisms for assembly of the nucleoplasmic reticulum.Cellular and molecular life sciences : CMLS · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. PML Body Biogenesis: A Delicate Balance of Interactions.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Running 'LAPS' Around nLD: Nuclear Lipid Droplet Form and Function.Frontiers in cell and developmental biology · 2022
    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

5 authors.

Jonghwa LeeDepartment of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Canada.
Jayme SalsmanDepartment of Pathology, Dalhousie University, Halifax, Canada.
Jason FosterDepartment of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Canada.
Graham DellaireDepartment of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Canada dellaire@dal.ca.ORCID 0000-0002-3466-6316
Neale D RidgwayDepartment of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Canada nridgway@dal.ca.ORCID 0000-0002-0441-6228

Funding

CIHR PJT62390
6 · The paper itself

Abstract

Nuclear lipid droplets (nLDs) form on the inner nuclear membrane by a mechanism involving promyelocytic leukemia (PML), the protein scaffold of PML nuclear bodies. We report that PML structures on nLDs in oleate-treated U2OS cells, referred to as lipid-associated PML structures (LAPS), differ from canonical PML nuclear bodies by the relative absence of SUMO1, SP100, and DAXX. These nLDs were also enriched in CTP:phosphocholine cytidylyltransferase α (CCTα), the phosphatidic acid phosphatase Lipin1, and DAG. Translocation of CCTα onto nLDs was mediated by its α-helical M-domain but was not correlated with its activator DAG. High-resolution imaging revealed that CCTα and LAPS occupied distinct polarized regions on nLDs. PML knockout U2OS (PML KO) cells lacking LAPS had a 40-50% reduction in nLDs with associated CCTα, and residual nLDs were almost devoid of Lipin1 and DAG. As a result, phosphatidylcholine and triacylglycerol synthesis was inhibited in PML KO cells. We conclude that in response to excess exogenous fatty acids, LAPS are required to assemble nLDs that are competent to recruit CCTα and Lipin1.

Indexed as

AnimalsCell NucleusCHO CellsCholine-Phosphate CytidylyltransferaseCricetulusFatty AcidsHumansLipid DropletsNuclear EnvelopeOleic AcidPhosphatidate PhosphatasePhosphatidylcholinesPromyelocytic Leukemia ProteinCholine-Phosphate CytidylyltransferaseFatty AcidsLPIN1 protein, humanOleic AcidPCYT1A protein, humanPhosphatidate PhosphatasePhosphatidylcholinesPML protein, humanPromyelocytic Leukemia Protein

Identifiers

PMID32461215
PMCPMC7266991

What OpenQuestion holds

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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.