Fine mapping of the human endothelin-converting enzyme gene by fluorescent in situ hybridization and radiation hybrids

Biochem Biophys Res Commun. 1996 Apr 25;221(3):682-7. doi: 10.1006/bbrc.1996.0656.

Abstract

Based on the sequence of the human endothelin-1-converting enzyme (hECE-1) cDNA, we cloned a 1982 bp cDNA fragment and we amplified by PCR a 3' fragment located on the last exon (exon 19). Human metaphase chromosomes were studied by Fluorescent in Situ Hybridization (FISH) using the 1982 digoxigenated hECE-1 fragment as a probe and chromosome 1-specific probes. Twin spot signals on each of the two homologous chromosomes 1 were found by FISH on band p36. The results of monochromosomal hybrids confirmed that hECE-1 is on chromosome 1. Radiation hybrid mapping localized the hECE-1 gene 3.15 cR far from D1S2436 (WI-3177), at about 25 cM from the telomere of the short arm, possibly at the border between 1p36.3 and 1p36.2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aspartic Acid Endopeptidases / genetics*
  • Aspartic Acid Endopeptidases / metabolism
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 1*
  • DNA, Complementary
  • Endothelin-Converting Enzymes
  • Humans
  • Hybrid Cells / radiation effects*
  • In Situ Hybridization
  • Metalloendopeptidases / metabolism
  • Molecular Sequence Data
  • Rodentia

Substances

  • DNA, Complementary
  • Aspartic Acid Endopeptidases
  • Metalloendopeptidases
  • Endothelin-Converting Enzymes