Acetyl-CoA–dependent processes are preferentially supported by local metabolite synthesis

The cell nucleus is an active metabolic site. Numerous enzymes best known for their roles in cytosolic or mitochondrial pathways also function in the nucleus, where they contribute to gene regulation and DNA replication and repair. Although metabolites can diffuse through nuclear pores, it remains unclear the extent to which the nucleus and cytosol operate as continuous versus distinct metabolic spaces. Both compartments require acetyl-CoA-for example, for histone acetylation and lipid synthesis-and the acetyl-CoA generating enzyme ATP-citrate lyase (ACLY) resides in both locations, but the significance of its dual localization is incompletely understood. Using cell lines in which ACLY is localized to either compartment, we find that ACLY in either location supports fatty acid synthesis and histone acetylation, yet compartment-localized ACLY enables finer control. Nuclear ACLY preserves histone H3K23 acetylation under glucose limitation and modulates specific transcriptional programs, whereas cytosolic ACLY most efficiently supports lipid biosynthetic fluxes. Thus, local synthesis defines a preferential metabolic fate, providing more precise regulation.

Authors

Institutions

Publication Details

Journal
Science Advances
Published
2026-09-11
DOI
https://doi.org/10.1126/sciadv.aee4935
Primary Topic
Sirtuins and Resveratrol in Medicine
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Acetyl-CoA–dependent processes are preferentially supported by local metabolite synthesis

Julianna Supplee, Mariola M. Marcinkiewicz, Christina Demetriadou, Karl A. Wessendorf-Rodriguez et al.
Science Advances
Sirtuins and Resveratrol in Medicine
article

Acetyl-CoA–dependent processes are preferentially supported by local metabolite synthesis

Julianna Supplee, Mariola M. Marcinkiewicz, Christina Demetriadou, Karl A. Wessendorf-Rodriguez, Pedro Costa‐Pinheiro, Christian M. Metallo, Simone Sidoli, Ronen Marmorstein, Nivitha Murali, Nathaniel W. Snyder, Stephanie Stransky, Kathryn E. Wellen, Jennifer L. Pennise, Qihua Yang, Joy Li
article en

Abstract

The cell nucleus is an active metabolic site. Numerous enzymes best known for their roles in cytosolic or mitochondrial pathways also function in the nucleus, where they contribute to gene regulation and DNA replication and repair. Although metabolites can diffuse through nuclear pores, it remains unclear the extent to which the nucleus and cytosol operate as continuous versus distinct metabolic spaces. Both compartments require acetyl-CoA-for example, for histone acetylation and lipid synthesis-and the acetyl-CoA generating enzyme ATP-citrate lyase (ACLY) resides in both locations, but the significance of its dual localization is incompletely understood. Using cell lines in which ACLY is localized to either compartment, we find that ACLY in either location supports fatty acid synthesis and histone acetylation, yet compartment-localized ACLY enables finer control. Nuclear ACLY preserves histone H3K23 acetylation under glucose limitation and modulates specific transcriptional programs, whereas cytosolic ACLY most efficiently supports lipid biosynthetic fluxes. Thus, local synthesis defines a preferential metabolic fate, providing more precise regulation.

Science AdvancesVol. 12(37)
Albert Einstein College of Medicine (US), Salk Institute for Biological Studies (US), La Jolla Bioengineering Institute (US), University of Pennsylvania (US), Temple University (US), Philadelphia University (US)
Hevolution Foundation, American Foundation for Aging Research, Ludwig Institute for Cancer Research, National Institutes of Health, NIH Office of the Director, National Cancer Institute
Openalex Percentile: Top 14%
Sirtuins and Resveratrol in Medicine
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.