The exit of naive pluripotency contains a metabolism-induced checkpoint for telomere homeostasis

During peri-implantation development, the pluripotent tissue of the early embryo undergoes profound cellular and biochemical reprogramming. These transformations are essential for subsequent development, yet how they are coordinated with the preservation of genome integrity remains poorly understood. Here, we uncover a telomere length checkpoint that is elicited by metabolic remodeling as mouse embryonic stem cells (ESCs) transition from the naive to formative pluripotent state. We show that the exit of naive pluripotency is marked by accelerated mitochondrial respiration and de novo lipogenesis, fueling lipid droplet accumulation required for tissue remodeling. Unexpectedly, these acute metabolic shifts trigger transient telomere shortening and activate ZSCAN4, a pluripotency-associated regulator of telomeres, followed by telomere re-elongation as cells adopt a more glycolytic metabolic profile. Our findings reveal a feedback mechanism in which metabolism-induced telomere stress engages ZSCAN4 as a protective response, thereby linking metabolic state to telomere homeostasis during early developmental progression.

Authors

Institutions

Publication Details

Journal
Cell Reports
Published
2025-12-01
DOI
https://doi.org/10.1016/j.celrep.2025.116654
Primary Topic
Telomeres, Telomerase, and Senescence
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The exit of naive pluripotency contains a metabolism-induced checkpoint for telomere homeostasis

Bryony J. Leeke, Megha Prakash Bangalore, Hendrik Marks, Michelle Percharde et al.
Cell Reports
Telomeres, Telomerase, and Senescence
article

The exit of naive pluripotency contains a metabolism-induced checkpoint for telomere homeostasis

Bryony J. Leeke, Megha Prakash Bangalore, Hendrik Marks, Michelle Percharde, David Barneda, Joop H. Jansen, James K. Ellis, Nick G.P. Bovee, Mark Christian, Clara Lopes Novo, Bebiana C. Sousa, Hector C. Keun, Donja Karimlou, Roshni A. de Souza, Mauricio Barahona, Andrea F. Lopez‐Clavijo, Véronique Azuara, Songyang Li, Yuhan Zheng, Zijing Liu, Eveline J.E.M. Kahlman
article en

Abstract

During peri-implantation development, the pluripotent tissue of the early embryo undergoes profound cellular and biochemical reprogramming. These transformations are essential for subsequent development, yet how they are coordinated with the preservation of genome integrity remains poorly understood. Here, we uncover a telomere length checkpoint that is elicited by metabolic remodeling as mouse embryonic stem cells (ESCs) transition from the naive to formative pluripotent state. We show that the exit of naive pluripotency is marked by accelerated mitochondrial respiration and de novo lipogenesis, fueling lipid droplet accumulation required for tissue remodeling. Unexpectedly, these acute metabolic shifts trigger transient telomere shortening and activate ZSCAN4, a pluripotency-associated regulator of telomeres, followed by telomere re-elongation as cells adopt a more glycolytic metabolic profile. Our findings reveal a feedback mechanism in which metabolism-induced telomere stress engages ZSCAN4 as a protective response, thereby linking metabolic state to telomere homeostasis during early developmental progression.

Cell ReportsVol. 44(12)
Babraham Institute (GB), Radboud University Nijmegen (NL), Radboud University Medical Center (NL), Radboud Institute for Molecular Life Sciences (NL), Imperial College London (GB)
Openalex Percentile: Top 51%
Telomeres, Telomerase, and Senescence
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.