Evidence map›Paper›PMID 40655553›Full record

ReviewFrontiers in plant science2025

Lipid droplets in plants: turnover and stress responses.

Yujie Zhao, Rui Cao, Jincheng Li, Yingying Xu, Lijuan Zhou, Yajin Ye

Erratum issuedAbstract readReview
In one paragraph

Review in Frontiers in plant science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Yujie ZhaoState Key Laboratory of Tree Genetics and Breeding, National Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China.
Rui CaoState Key Laboratory of Tree Genetics and Breeding, National Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China.
Jincheng LiState Key Laboratory of Tree Genetics and Breeding, National Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China.
Yingying XuState Key Laboratory of Tree Genetics and Breeding, National Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China.
Lijuan ZhouState Key Laboratory of Tree Genetics and Breeding, National Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China.
Yajin YeState Key Laboratory of Tree Genetics and Breeding, National Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid droplets (LDs) have emerged as dynamic organelles central to plant lipid metabolism, stress adaptation, and energy homeostasis. This review synthesizes recent advances in understanding LD biogenesis and degradation in plants, highlighting conserved and divergent mechanisms relative to other eukaryotes. LD formation originates in the endoplasmic reticulum (ER), where neutral lipids synthesized by diacylglycerol acyltransferases (DGAT) and phospholipid: diacylglycerol acyltransferases (PDAT) accumulate into lens-like structures. These structures bud into the cytosol via ER machinery, including SEIPIN complexes, vesicle-associated membrane proteins, and LD-associated protein-interacting protein which regulate LD size and abundance. Degradation occurs through two major pathways: lipolysis, mainly mediated by the patatin-like lipase SUGAR-DEPENDENT1, and lipophagy, where AUTOPHAGY-RELATED proteins deliver LDs for breakdown. LDs also function as stress-responsive hubs, accumulating under abiotic stresses and during pathogen interactions, where they participate in membrane remodeling and antimicrobial defense. Extensive studies in major oilseed crops reveal that expressions of multiple genes involved in LD turnover are significantly induced under various abiotic stresses and phytohormone treatments. These genetic components operate autonomously or synergistically (e.g. DGAT and PDAT) within the TAG biosynthesis and LD metabolic pathways, effecting concurrent enhancements in stress resilience and oil production under suboptimal growth conditions. Critical knowledge gaps persist, including the interplay between lipolysis and lipophagy, the integration of energy-related signaling pathways in LD turnover, and stress-modulated post-translational control of LD proteome. Deciphering these mechanisms will advance our understanding towards LD biology.

Indexed as

biogenesisdegradationlipid dropletslipophagySDP1stress responses

Identifiers

PMID40655553
PMCPMC12247314

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.