Chromosomal localization of the genes for human carboxypeptidase D (CPD) and the active 50-kilodalton subunit of human carboxypeptidase N (CPN1)

Genomics. 1998 May 15;50(1):105-8. doi: 10.1006/geno.1998.5295.

Abstract

Human carboxypeptidase N is a 280-kDa tetrameric enzyme consisting of two 83-kDa regulatory subunits and two catalytic 50-kDa subunits. The 83-kDa subunit is a member of the leucine-rich repeat family of proteins and has been localized to chromosome 8p22-p23. The 50-kDa subunit is a member of the regulatory B-type carboxypeptidase family, which includes carboxypeptidases M, E/H, AEBP1, and a newly described member, carboxypeptidase D, which has three tandem active site domains. The human genes for carboxypeptidase D (HGMW-approved symbol CPD) and the 50-kDa subunit of carboxypeptidase N (HGMW-approved symbol CPN1) were localized to chromosomes 17 and 10, respectively, using the polymerase chain reaction with gene-specific primers and DNAs derived from somatic cell hybrids. The carboxypeptidase D gene was further localized to the centromeric region 17p11.1-q11.1/11.2 by use of a regional mapping panel derived from somatic cell hybrids containing different portions of chromosome 17.

Publication types

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

MeSH terms

  • Carboxypeptidases / genetics*
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 17 / genetics
  • Humans
  • Hybrid Cells / chemistry
  • Hybrid Cells / cytology
  • Lysine Carboxypeptidase / genetics*
  • Molecular Weight

Substances

  • Carboxypeptidases
  • carboxypeptidase D
  • Lysine Carboxypeptidase