Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3

Genomics. 1995 Apr 10;26(3):550-5. doi: 10.1016/0888-7543(95)80174-k.

Abstract

We have isolated and characterized cDNA clones encoding a novel human homeobox gene, MOX2, the homologue of the murine mox-2 gene. The MOX2 protein contains all of the characteristic features of Mox-2 proteins of other vertebrate species, namely the homeobox, the polyhistidine stretch, and a number of potential serine/threonine phosphorylation sites. The homeodomain of MOX2 protein is identical to all other vertebrate species reported so far (rodents and amphibians). Outside the homeodomain, Mox-2 proteins share a high degree of identity, except for a few amino acid differences encountered between the human and the rodent polypeptides. A polyhistidine stretch of 12 amino acids in the N terminal region of the protein is also conserved among humans, rodents, and (only partly) amphibians. The chromosomal position of MOX2 was assigned to 7p22.1-p21.3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 7*
  • DNA, Complementary
  • Genes, Homeobox*
  • Homeodomain Proteins / genetics*
  • Humans
  • Mice
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Sequence Alignment

Substances

  • DNA, Complementary
  • Homeodomain Proteins
  • MEOX2 protein, human
  • Meox2 protein, mouse

Associated data

  • GENBANK/X82629