Characterization of mpl cytoplasmic domain sequences required for myeloproliferative leukemia virus pathogenicity

J Virol. 1994 Aug;68(8):5270-4. doi: 10.1128/JVI.68.8.5270-5274.1994.

Abstract

v-mpl is a truncated form of a receptor-like chain which belongs to the cytokine receptor superfamily. This sequence has been transduced in the myeloproliferative leukemia virus as an env-mpl fusion gene responsible for an acute myeloproliferative disorder in mice. We constructed a series of viral mutants in the mpl sequence. Analysis of their oncogenic potential in vivo indicated that a critical 69-amino-acid-long cytoplasmic domain of v-Mpl is required for myoproliferative leukemia virus pathogenicity. We also developed an in vitro assay and showed that expression of the env-mpl gene confers growth factor independence to murine as well as to human hematopoietic growth factor-dependent cell lines. These findings strongly suggest that v-Mpl delivers a constitutive proliferative signal through a limited region of its cytoplasmic domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Amino Acid Sequence
  • Animals
  • Cloning, Molecular
  • Cytoplasm / chemistry
  • Defective Viruses / genetics
  • Defective Viruses / pathogenicity
  • Leukemia Virus, Murine / genetics
  • Leukemia Virus, Murine / pathogenicity*
  • Mice
  • Molecular Sequence Data
  • Mutagenesis
  • Retroviridae Proteins, Oncogenic / chemistry
  • Retroviridae Proteins, Oncogenic / genetics*

Substances

  • Retroviridae Proteins, Oncogenic