4.4 Review

Antizyme inhibitor 2: molecular, cellular and physiological aspects

Journal

AMINO ACIDS
Volume 38, Issue 2, Pages 603-611

Publisher

SPRINGER WIEN
DOI: 10.1007/s00726-009-0419-4

Keywords

Antizymes; Antizyme inhibitor 2; Polyamines; Ornithine decarboxylase like; Arginine decarboxylase; Spermiogenesis

Funding

  1. Seneca Foundation (Autonomous Community of Murcia) [08681/PI/08]
  2. Spanish Ministry of Science and Innovation [SAF2008-03638]
  3. FEDER

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Polyamines are small organic polycations essential for cell proliferation and survival. Antizymes (AZs) are small proteins regulated by polyamines that inhibit polyamine biosynthesis and uptake in mammalian cells. In addition, antizyme functions are also regulated by antizyme inhibitors, homologue proteins of ornithine decarboxylase lacking enzymatic activity. There are two antizyme inhibitors (AZIN), known as AZIN1 and AZIN2, that bind to AZs and negate their effects on polyamine metabolism. Here, we review different molecular and cellular properties of the novel AZIN2 with particular emphasis on the role that this protein may have in brain and testis physiology. Whereas AZIN1 is ubiquitously found in mammalian tissues, AZIN2 expression appears to be restricted to brain and testis. In transfected cells, AZIN2 is mainly located in the endoplasmic reticulum-Golgi intermediate compartment and in the cis-Golgi network. AZIN2 is a labile protein that is degraded by the proteasome by a ubiquitin-dependent mechanism. Regarding its physiological role, spatial and temporal analyses of AZIN2 expression in the mouse testis suggest that this protein may have a role in spermiogenesis.

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