PHD1 interacts with ATF4 and negatively regulates its transcriptional activity without prolyl hydroxylation

Yusuke Hiwatashi, Kohei Kanno, Chikahisa Takasaki, Kenji Goryo, Takuya Sato, Satoru Torii, Kazuhiro Sogawa, Ken ichi Yasumoto

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)


Cellular response to hypoxia plays an important role in both circulatory and pulmonary diseases and cancer. Hypoxia-inducible factors (HIFs) are major transcription factors regulating the response to hypoxia. The α-subunits of HIFs are hydroxylated by members of the prolyl-4-hydroxylase domain (PHD) family, PHD1, PHD2, and PHD3, in an oxygen-dependent manner. Here, we report on the identification of ATF4 as a protein interacting with PHD1 as well as PHD3, but not with PHD2. The central region of ATF4 including the Zipper II domain, ODD domain and β-TrCP recognition motif were involved in the interaction with PHD1. Coexistence of PHD1 stabilized ATF4, as opposed to the destabilization of ATF4 by PHD3. Moreover, coexpression of ATF4 destabilized PHD3, whereas PHD1 stability was not affected by the presence of ATF4. Mutations to alanine of proline residues in ATF4 that satisfied hydroxylation consensus by PHDs did not affect binding activity of ATF4 to PHD1 and PHD3. Furthermore, in vitro prolyl hydroxylation assay clearly indicated that ATF4 did not serve as a substrate of both PHD1 and PHD3. Coexpression of PHD1 or PHD3 with ATF4 repressed the transcriptional activity of ATF4. These results suggest that PHD1 and PHD3 control the transactivation activity of ATF4.

Original languageEnglish
Pages (from-to)2789-2799
Number of pages11
JournalExperimental Cell Research
Issue number20
Publication statusPublished - 2011 Dec 10


  • ATF4
  • HIF prolyl hydroxylation
  • Hypoxia
  • PHD1
  • PHD3


Dive into the research topics of 'PHD1 interacts with ATF4 and negatively regulates its transcriptional activity without prolyl hydroxylation'. Together they form a unique fingerprint.

Cite this