8EZ6

The DBC1/SIRT1 Interaction is Choreographed by Post-translational Modification

8EZ6 の概要

• エントリーDOI: 10.2210/pdb8ez6/pdb
• 分子名称: Cell cycle and apoptosis regulator protein 2 (2 entities in total)
• 機能のキーワード: dbc1, s1-like, insulin signaling, liver metabolism, chaperone, gene regulation
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 16000.15

構造登録者

Krzysiak, T.C.,Gronenborn, A.M. (登録日: 2022-10-31, 公開日: 2024-03-27, 最終更新日: 2026-03-04)

主引用文献

Krzysiak, T.C.,Choi, Y.J.,Kim, Y.J.,Yang, Y.,DeHaven, C.,Thompson, L.,Ponticelli, R.,Mermigos, M.M.,Thomas, L.,Marquez, A.,Sipula, I.,Kemper, J.K.,Jurczak, M.,Thomas, G.,Gronenborn, A.M.
Inhibitory protein-protein interactions of the SIRT1 deacetylase are choreographed by post-translational modification.
Protein Sci., 33:e4938-e4938, 2024

PubMed Abstract: Regulation of SIRT1 activity is vital to energy homeostasis and plays important roles in many diseases. We previously showed that insulin triggers the epigenetic regulator DBC1 to prime SIRT1 for repression by the multifunctional trafficking protein PACS-2. Here, we show that liver DBC1/PACS-2 regulates the diurnal inhibition of SIRT1, which is critically important for insulin-dependent switch in fuel metabolism from fat to glucose oxidation. We present the x-ray structure of the DBC1 S1-like domain that binds SIRT1 and an NMR characterization of how the SIRT1 N-terminal region engages DBC1. This interaction is inhibited by acetylation of K112 of DBC1 and stimulated by the insulin-dependent phosphorylation of human SIRT1 at S162 and S172, catalyzed sequentially by CK2 and GSK3, resulting in the PACS-2-dependent inhibition of nuclear SIRT1 enzymatic activity and translocation of the deacetylase in the cytoplasm. Finally, we discuss how defects in the DBC1/PACS-2-controlled SIRT1 inhibitory pathway are associated with disease, including obesity and non-alcoholic fatty liver disease.

PubMed: 38533551
DOI: 10.1002/pro.4938

実験手法

X-RAY DIFFRACTION (2 Å)