SIRT1 suppresses activating transcription factor 4 (ATF4) expression in response to proteasome inhibition

Seon Rang Woo, Jeong Eun Park, Yang Hyun Kim, Yeun Jin Ju, Hyun Jin Shin, Hyun Yoo Joo, Eun Ran Park, Sung Hee Hong, Gil Hong Park, Kee Ho Lee

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)


The synthetic machinery of ATF4 (activating transcription factor 4) is activated in response to various stress conditions involved in nutrient restriction, endoplasmic reticulum homeostasis, and oxidation. Stress-induced inhibition of proteasome activity triggers the unfolded protein response and endoplasmic reticulum stress, where ATF4 is crucial for consequent biological events. In the current study, we showed that the NAD+-dependent deacetylase, SIRT1, suppresses ATF4 synthesis during proteasome inhibition. SIRT1 depletion via transfection of specific siRNA into HeLa cells resulted in a significant increase in ATF4 protein, which was observed specifically in the presence of the proteasome inhibitor MG132. Consistent with SIRT1 depletion data, transient transfection of cells with SIRT1-overexpressing plasmid induced a decrease in the ATF4 protein level in the presence of MG132. Interestingly, however, ATF4 mRNA was not affected by SIRT1, even in the presence of MG132, indicating that SIRT1-induced suppression of ATF4 synthesis occurs under post-transcriptional control. Accordingly, we propose that SIRT1 serves as a negative regulator of ATF4 protein synthesis at the post-transcriptional level, which is observed during stress conditions, such as proteasome inhibition.

Original languageEnglish
Pages (from-to)1785-1790
Number of pages6
JournalJournal of microbiology and biotechnology
Issue number12
Publication statusPublished - 2013
Externally publishedYes


  • ATF4
  • Deacetylase
  • Proteasome inhibition
  • SIRT1
  • Stress

ASJC Scopus subject areas

  • Biotechnology
  • Applied Microbiology and Biotechnology


Dive into the research topics of 'SIRT1 suppresses activating transcription factor 4 (ATF4) expression in response to proteasome inhibition'. Together they form a unique fingerprint.

Cite this