1. Academic Validation
  2. Precursor of pro-apoptotic cytokine modulates aminoacylation activity of tRNA synthetase

Precursor of pro-apoptotic cytokine modulates aminoacylation activity of tRNA synthetase

  • J Biol Chem. 1999 Jun 11;274(24):16673-6. doi: 10.1074/jbc.274.24.16673.
S G Park 1 K H Jung J S Lee Y J Jo H Motegi S Kim K Shiba
Affiliations

Affiliation

  • 1 National Creative Research Initiatives Center for ARS Network, Sung Kyun Kwan University, Suwon, Kyunggido, 440-746, Korea.
Abstract

Endothelial monocyte activating polypeptide II (EMAPII) is a cytokine that is specifically induced by Apoptosis. Its precursor (pro-EMAPII) has been suggested to be identical to p43, which is associated with the multi-tRNA synthetase complex. Herein, we have demonstrated that the N-terminal domain of pro-EMAPII interacts with the N-terminal extension of human cytoplasmic arginyl-tRNA synthetase (RRS) using genetic and immunoprecipitation analyses. Aminoacylation activity of RRS was enhanced about 2.5-fold by the interaction with pro-EMAPII but not with its N- or C-terminal domains alone. The N-terminal extension of RRS was not required for Enzyme activity but did mediate activity stimulation by pro-EMAPII. Pro-EMAPII reduced the apparent Km of RRS to tRNA, whereas the kcat value remained unchanged. Therefore, the precursor of EMAPII is a multi-functional protein that assists aminoacylation in normal cells and releases the functional cytokine upon Apoptosis.

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