Evidence map›Paper›PMID 38316990›Full record

ArticleThe EMBO journal2024

The DDHD2-STXBP1 interaction mediates long-term memory via generation of saturated free fatty acids.

Isaac O Akefe, Saber H Saber, Benjamin Matthews, Bharat G Venkatesh, Rachel S Gormal, Daniel G Blackmore, Suzy Alexander, Emma Sieriecki, Yann Gambin, Jesus Bertran-Gonzalez and 10 more

Open access · diamondAbstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Neurons run on fat.npj metabolic health and disease · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. DDHD2 possesses both lipase and transacylase capacities that remodel triglyceride acyl chains.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Microglia-to-neuron signaling linksProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

20 authors at 5 institutions in 3 countries.

Isaac O Akefe *Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-4738-0701
Saber H Saber *Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-1296-2023
Benjamin Matthews *Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.
Bharat G VenkateshClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-1003-1970
Rachel S GormalClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-1604-0253
Daniel G BlackmoreClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.
Suzy AlexanderClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.
Emma SierieckiSchool of Medical Science, University of New South Wales, Randwick, NSW, 2052, Australia.ORCID http://orcid.org/0000-0001-9970-868X
Yann GambinSchool of Medical Science, University of New South Wales, Randwick, NSW, 2052, Australia.
Jesus Bertran-GonzalezDecision Neuroscience Lab, School of Psychology, UNSW Sydney, Sydney, Australia.
Nicolas VitaleInstitut des Neurosciences Cellulaires et Intégratives, UPR-3212 CNRS - Université de Strasbourg, Strasbourg, France.ORCID http://orcid.org/0000-0002-4752-4907
Yann HumeauInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, Université de Bordeaux, Bordeaux, France.
Arnaud GaudinClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.ORCID http://orcid.org/0000-0002-6644-1824
Sevannah A EllisClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-2304-8763
Alysee A MichaelsDepartment of Neuroscience, Baylor College of Medicine, Houston, TX, USA.
Mingshan XueDepartment of Neuroscience, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0003-1463-8884
Benjamin CravattThe Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA, USA.
Merja JoensuuClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia. m.joensuu@uq.edu.au.ORCID http://orcid.org/0000-0002-4533-0455
Tristan P WallisClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia. t.wallis@uq.edu.au.ORCID http://orcid.org/0000-0002-6515-9157
Frédéric A MeunierClem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, 4072, Australia. f.meunier@uq.edu.au.ORCID http://orcid.org/0000-0001-6400-1107
The University of Queensland · AUUNSW Sydney · AUBaylor College of Medicine · USCentre National de la Recherche Scientifique · FRScripps Research Institute · US

Funding

Department of Education and Training | Australian Research Council (ARC) DE190100565DHAC | National Health and Medical Research Council (NHMRC) 2010901DHAC | National Health and Medical Research Council (NHMRC) GNT1155794
6 · The paper itself

Abstract

The phospholipid and free fatty acid (FFA) composition of neuronal membranes plays a crucial role in learning and memory, but the mechanisms through which neuronal activity affects the brain's lipid landscape remain largely unexplored. The levels of saturated FFAs, particularly of myristic acid (C14:0), strongly increase during neuronal stimulation and memory acquisition, suggesting the involvement of phospholipase A1 (PLA1) activity in synaptic plasticity. Here, we show that genetic ablation of the PLA1 isoform DDHD2 in mice dramatically reduces saturated FFA responses to memory acquisition across the brain. Furthermore, DDHD2 loss also decreases memory performance in reward-based learning and spatial memory models prior to the development of neuromuscular deficits that mirror human spastic paraplegia. Via pulldown-mass spectrometry analyses, we find that DDHD2 binds to the key synaptic protein STXBP1. Using STXBP1/2 knockout neurosecretory cells and a haploinsufficient STXBP1

Indexed as

Fatty Acids, NonesterifiedMemory, Long-TermMunc18 ProteinsPhospholipasesAnimalsBrainMemoryMiceDDHD2 protein, mouseFatty Acids, NonesterifiedMunc18 ProteinsPhospholipasesStxbp1 protein, mouseFree Fatty AcidsLearning and MemoryLipidsMyristic AcidPhospholipase A1

Identifiers

PMID38316990
PMCPMC10897203
OpenAlexW4391543819

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.