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Merck

Cloning and characterization of a novel RING-B-box-coiled-coil protein with apoptotic function.

The Journal of biological chemistry (2003-04-15)
Fumihiko Kimura, Shinya Suzu, Yukitsugu Nakamura, Yukiko Nakata, Muneo Yamada, Naruo Kuwada, Takuya Matsumura, Takuya Yamashita, Takashi Ikeda, Ken Sato, Kazuo Motoyoshi
RESUMEN

We have identified a novel RING-B-box-coiled-coil (RBCC) protein (MAIR for macrophage-derived apoptosis-inducing RBCC protein) that consists of an N-terminal RING finger, followed by a B-box zinc finger, a coiled-coil domain, and a B30.2 domain. MAIR mRNA was expressed widely in mouse tissues and was induced by macrophage colony-stimulating factor in murine peritoneal and bone marrow macrophages. MAIR protein initially showed a granular distribution predominantly in the cytoplasm. The addition of zinc to transfectants containing MAIR cDNA as part of a heavy metal-inducible vector caused apoptosis of the cells characterized by cell fragmentation; a reduction in mitochondrial membrane potential; activation of caspase-7, -8, and -9, but not caspase-3; and DNA degradation. We also found that the RING finger and coiled-coil domains were required for MAIR activity by analysis with deletion mutants.