Regional chromosomal localization of the human gene for galactose-1-phosphate uridyltransferase

Hum Genet. 1977 Jul 26;37(3):279-84. doi: 10.1007/BF00393609.

Abstract

In the progeny of somatic cell hybrids formed by fusion of human lymphocytes and Chinese hamster mutant cells, a single human chromosome A2 was selectively retained when grown in appropriate medium. Spontaneous breakage of this chromosome in different hybrid subclones led to the assignment of the gene for galactose-1-phosphate uridyltransferase to the centromeric region of this chromosome (2q11 leads to 2q14). This gene is shown to be syntenic to the previously mapped genes for acid phosphatase 1 and malate dehydrogenase 1.

Publication types

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

MeSH terms

  • Acid Phosphatase
  • Animals
  • Chromosome Mapping
  • Chromosomes, Human, 1-3*
  • Cricetinae
  • Genes
  • Humans
  • Hybrid Cells
  • Lymphocytes
  • Malate Dehydrogenase
  • Male
  • Mutation
  • Nucleotidyltransferases*
  • UDPglucose-Hexose-1-Phosphate Uridylyltransferase*

Substances

  • Malate Dehydrogenase
  • Nucleotidyltransferases
  • UDPglucose-Hexose-1-Phosphate Uridylyltransferase
  • Acid Phosphatase