Tumor suppressor NPRL2 induces ROS production and DNA damage response

Yinxing Ma, Licia Silveri, John LaCava, Svetlana Dokudovskaya*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

6 Citations (Scopus)
18 Downloads (Pure)

Abstract

The SEA/GATOR complex is an essential regulator of the mTORC1 pathway. In mammals the GATOR1 complex is composed of the proteins DEPDC5, NPRL2 and NPRL3. GATOR1 serves as an mTORC1 inhibitor and activates the mTORC1-modulating RagA GTPase. However, several GATOR members have mTORC1 independent functions. Here we characterize mammalian cells overexpressing the GATOR1 component NPRL2. We demonstrate that, in the cells with active p53, ectopic expression of NPRL2 induces NOX2-dependent production of reactive oxygen species and DNA damage. Overexpressed NPRL2 accumulates in the nucleus, together with apoptosis-inducing factor (AIF). These events are accompanied by phosphorylation of p53, activation of a DNA-damage response and cell cycle arrest in G1 phase, followed by apoptosis. In the cells negative for active p53, NPRL2 ectopic expression leads to activation of CHK1 or CHK2 kinases and cell cycle arrest in S or G2/M phases. Combined, these results demonstrate a new role for the NPRL2, distinct from its function in mTORC1 regulation.

Original languageEnglish
Article number15311
Number of pages15
JournalScientific Reports
Volume7
DOIs
Publication statusPublished - 10-Nov-2017
Externally publishedYes

Keywords

  • SEA COMPLEX
  • MAMMALIAN TARGET
  • G(1) ARREST
  • TORC1
  • GENE
  • AUTOPHAGY
  • PROTEIN
  • MECHANISMS
  • RESISTANCE
  • STARVATION

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