N-myc can functionally replace c-myc in murine development, cellular growth, and differentiation

Genes Dev. 2000 Jun 1;14(11):1390-9.

Abstract

Members of the myc family of cellular oncogenes have been implicated as transcriptional regulators in pathways that govern cellular proliferation and death. In addition, N-myc and c-myc are essential for completion of murine embryonic development. However, the basis for the evolutionary conservation of myc gene family has remained unclear. To elucidate this issue, we have generated mice in which the endogenous c-myc coding sequences have been replaced with N-myc coding sequences. Strikingly, mice homozygous for this replacement mutation can survive into adulthood and reproduce. Moreover, when expressed from the c-myc locus, N-myc is similarly regulated and functionally complementary to c-myc in the context of various cellular growth and differentiation processes. Therefore, the myc gene family must have evolved, to a large extent, to facilitate differential patterns of expression.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Animals
  • Animals, Newborn
  • Bone Marrow / metabolism
  • CD3 Complex / metabolism
  • Cell Differentiation
  • Cell Division
  • Concanavalin A / metabolism
  • Exons
  • Flow Cytometry
  • Genes, myc / genetics*
  • Genes, myc / physiology*
  • Genotype
  • Lipopolysaccharides / metabolism
  • Lymphocytes / cytology
  • Mice / embryology*
  • Mice, Transgenic
  • Models, Genetic
  • Muscle, Skeletal / metabolism
  • Mutagenesis
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • Proto-Oncogene Proteins c-myc / physiology*
  • Spleen / metabolism
  • Stem Cells / metabolism
  • Thymus Gland / metabolism
  • Time Factors
  • Tissue Distribution

Substances

  • CD3 Complex
  • Lipopolysaccharides
  • Proto-Oncogene Proteins c-myc
  • Concanavalin A