Evidence map›Paper›PMID 32530796›Full record

ReviewMolecular biology of the cell2020

Lipid and protein dynamics that shape nuclear envelope identity.

Shirin Bahmanyar, Christian Schlieker

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular biology of the cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Mechanisms for assembly of the nucleoplasmic reticulum.Cellular and molecular life sciences : CMLS · 2024
    Review
  10. Article
  11. Article
  12. The role of lipids in genome integrity and pluripotency.Biochemical Society transactions · 2024
    Review
  13. Review
  14. Article
  15. Review
  16. Nuclear envelope budding: Getting large macromolecular complexes out of the nucleus.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Shirin BahmanyarDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520.
Christian SchliekerDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, CT 06520.
Yale University · US

Funding

Defining the role of lipid metabolism in nuclear envelope identity and dynamicsR01GM131004 · NIGMS · YALE UNIVERSITY · PI Shirin Bahmanyar · 2019 to 2026
$2.8M
Structure-function analysis of Torsin ATPases in the context of the membraneR01GM114401 · NIGMS · YALE UNIVERSITY · PI SCHLIEKER, CHRISTIAN DIRK · 2016 to 2019
$1.3M
Defining the nuclear envelope-resident protein turnover machinery implicated in diseases affecting cholesterol metabolismR01GM126835 · NIGMS · YALE UNIVERSITY · PI SCHLIEKER, CHRISTIAN DIRK · 2018 to 2021
$1.3M
National Science Foundation 1846010NIGMS NIH HHS R01 GM114401NIGMS NIH HHS R01 GM126835NIGMS NIH HHS R01 GM131004
6 · The paper itself

Abstract

The nuclear envelope (NE) is continuous with the endoplasmic reticulum (ER), yet the NE carries out many functions distinct from those of bulk ER. This functional specialization depends on a unique protein composition that defines NE identity and must be both established and actively maintained. The NE undergoes extensive remodeling in interphase and mitosis, so mechanisms that seal NE holes and protect its unique composition are critical for maintaining its functions. New evidence shows that closure of NE holes relies on regulated de novo lipid synthesis, providing a link between lipid metabolism and generating and maintaining NE identity. Here, we review regulation of the lipid bilayers of the NE and suggest ways to generate lipid asymmetry across the NE despite its direct continuity with the ER. We also discuss the elusive mechanism of membrane fusion during nuclear pore complex (NPC) biogenesis. We propose a model in which NPC biogenesis is carefully controlled to ensure that a permeability barrier has been established before membrane fusion, thereby avoiding a major threat to compartmentalization.

Indexed as

Lipid MetabolismAnimalsCell CycleHumansLipid BilayersMembrane FusionMitosisNuclear EnvelopeLipid Bilayers

Identifiers

PMID32530796
PMCPMC7353140
OpenAlexW3034444949

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.