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noxin, a novel stress-induced gene involved in cell cycle and apoptosis

  • Naoki Nakaya
  • , Jill Hemish
  • , Peter Krasnov
  • , Sang Yong Kim
  • , Yuri Stasiv
  • , Tatyana Michurina
  • , Daniel Herman
  • , Michail S. Davidoff
  • , Ralf Middendorff
  • , Grigori Enikolopov
  • Cold Spring Harbor Laboratory
  • Stony Brook University
  • University of Hamburg
  • Justus Liebig University Giessen

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

We describe a novel stress-induced gene, noxin, and a knockout mouse line with an inactivated noxin gene. The noxin gene does not have sequelogs in the genome and encodes a highly serine-rich protein with predicted phosphorylation sites for ATM, Akt, and DNA-dependent protein kinase kinases; nuclear localization signals; and a Zn finger domain. noxin mRNA and protein levels are under tight control by the cell cycle. noxin, identified as a nitric oxide-inducible gene, is strongly induced by a wide range of stress signals: γ- and UV irradiation, hydrogen peroxide, adriamycin, and cytokines. This induction is dependent on p53. Noxin accumulates in the nucleus in response to stress and, when ectopically expressed, Noxin arrests the cell cycle at G 1; although it also induces p53, the cell cycle arrest function of Noxin is independent of p53 activity. noxin knockout mice are viable and fertile; however, they have an enlarged heart, several altered hematopoietic parameters, and a decreased number of spermatids. Importantly, loss or downregulation of Noxin leads to increased cell death. Our results suggest that Noxin may be a component of the cell defense system: it is activated by various stress stimuli, helps cells to withdraw from cycling, and opposes apoptosis.

Original languageEnglish
Pages (from-to)5430-5444
Number of pages15
JournalMolecular and Cellular Biology
Volume27
Issue number15
DOIs
StatePublished - Aug 2007

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