MVP interacts with YPEL4 and inhibits YPEL4-mediated activities of the ERK signal pathway

Biochem Cell Biol. 2010 Jun;88(3):445-50. doi: 10.1139/o09-166.

Abstract

Human YPEL4 is a member of YPEL family. It contains a Yippee domain, which is a putative zinc-finger-like, metal-binding domain. The human YPEL4 gene maps to chromosome 11q12.1, is ubiquitously expressed in adult tissues, and encodes a nuclear protein of 127 amino acids, the function of which remains unknown. To gain insights into the cellular function of this protein, we searched for YPEL4-interacting proteins using a yeast two-hybrid screen. The major vault protein (MVP), a lung resistance associated protein, was identified as a binding partner of YPEL4. The interaction between YPEL4 and MVP in mammalian cells was further demonstrated by a series of biochemical assays including the mammalian two-hybrid assay, GST pull-down assay, co-immunoprecipitation assay, and immunocytochemistry. Using a reporter system, we found that MVP can inhibit YPEL4's ability to activate Elk-1 in the MAPK signaling pathway. This study provides new clues for understanding the molecular mechanism of YPEL4 in cell division and signal transduction pathways and should be helpful for understanding molecular functions of the YPEL family.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Carrier Proteins / antagonists & inhibitors
  • Carrier Proteins / metabolism*
  • Cells, Cultured
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • MAP Kinase Signaling System*
  • Microscopy, Fluorescence
  • Vault Ribonucleoprotein Particles / metabolism*
  • Zinc Fingers

Substances

  • Carrier Proteins
  • Vault Ribonucleoprotein Particles
  • YPEL4 protein, human
  • major vault protein
  • Extracellular Signal-Regulated MAP Kinases