Structure and localization of the gene encoding human peripheral myelin protein 2 (PMP2)

Genomics. 1993 Nov;18(2):244-8. doi: 10.1006/geno.1993.1462.

Abstract

Peripheral myelin protein 2 (PMP2) is a small, basic, and cytoplasmic lipid binding protein of peripheral myelin. In this paper, we describe the cloning, characterization, and chromosomal mapping of the human PMP2 gene. The gene is about 8 kb long and consists of four exons. All exon-intron junction sequences conform to the GT/AG rule. The 5'-flanking region of the gene has a TA-rich element (TATA-like box) and a single defined transcription initiation site detected by the primer extension method. The gene for human PMP2 was assigned to chromosome 8q21.3-q22.1 by spot hybridization of flow-sorted human chromosomes and fluorescence in situ hybridization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chromosomes, Human, Pair 8*
  • Cloning, Molecular
  • DNA
  • Exons
  • Humans
  • In Situ Hybridization, Fluorescence
  • Introns
  • Molecular Sequence Data
  • Myelin Proteins / genetics*
  • Restriction Mapping
  • TATA Box
  • Transcription, Genetic

Substances

  • Myelin Proteins
  • DNA

Associated data

  • GENBANK/D16179
  • GENBANK/D16180
  • GENBANK/D16181