G protein‐coupled oestrogen receptor regulates branched‐chain amino acid metabolism through c‐Jun N‐terminal kinase

Branched-chain amino acids (BCAA) are essential requirements for overall protein turnover, signalling and energy balance, and dysregulation of their metabolic pathway has been associated with many pathophysiological events. Despite the importance of BCAA in human health, our understanding of their metabolic regulation is limited. Here, we present evidence that G protein-coupled oestrogen receptor (GPER) activation inhibits the key BCAA metabolic regulatory enzyme branched-chain α-keto acid dehydrogenase complex (BCKDH) by phosphorylating S293. Inhibition of BCKDH results in leucine, isoleucine and valine accumulation in cells. Interestingly, GPER did not alter the levels of the kinase BCKDK and the phosphatase PPM1K, which regulate BCKDH activity, but activated MAPK signalling. Using gene silencing, we identified that JNK intercedes GPER-mediated BCKDH inhibition. Together, our results demonstrate that GPER inhibits BCAA metabolism through JNK signalling.

Authors

Institutions

Publication Details

Journal
FEBS Letters
Published
2025-03-01
DOI
https://doi.org/10.1002/1873-3468.70030
Citations
1
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
0.94

Funders

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

G protein‐coupled oestrogen receptor regulates branched‐chain amino acid metabolism through c‐Jun N‐terminal kinase

Roshan M. Borkar, Sachin B. Jorvekar, Sudhagar Selvaraju, Anshu Gupta et al.
1 citations
FEBS Letters
Cancer, Hypoxia, and Metabolism
0.94
article

G protein‐coupled oestrogen receptor regulates branched‐chain amino acid metabolism through c‐Jun N‐terminal kinase

Roshan M. Borkar, Sachin B. Jorvekar, Sudhagar Selvaraju, Anshu Gupta, M. Chandrasekaran, Prasad Govind Shinde, Akash Suresh Humane
article en
1 citations

Abstract

Branched-chain amino acids (BCAA) are essential requirements for overall protein turnover, signalling and energy balance, and dysregulation of their metabolic pathway has been associated with many pathophysiological events. Despite the importance of BCAA in human health, our understanding of their metabolic regulation is limited. Here, we present evidence that G protein-coupled oestrogen receptor (GPER) activation inhibits the key BCAA metabolic regulatory enzyme branched-chain α-keto acid dehydrogenase complex (BCKDH) by phosphorylating S293. Inhibition of BCKDH results in leucine, isoleucine and valine accumulation in cells. Interestingly, GPER did not alter the levels of the kinase BCKDK and the phosphatase PPM1K, which regulate BCKDH activity, but activated MAPK signalling. Using gene silencing, we identified that JNK intercedes GPER-mediated BCKDH inhibition. Together, our results demonstrate that GPER inhibits BCAA metabolism through JNK signalling.

FEBS LettersVol. 599(6)
National Institute of Pharmaceutical Education and Research (IN)
Indian Council of Medical Research
Affordable and clean energy
Openalex Percentile: Top 28%
Cancer, Hypoxia, and Metabolism
0.94
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.

G protein‐coupled oestrogen receptor regulates branched‐chain amino acid metabolism through c‐Jun N‐terminal kinase — Roshan M. Borkar, Sachin B. Jorvekar, et al. · FEBS Letters (2025) | TGRS Research Map | TGRS