Assignment of the human poly(A) polymerase (PAP) gene to chromosome 14q32.1-q32.2 and isolation of a polymorphic CA repeat sequence

J Hum Genet. 1999;44(4):253-5. doi: 10.1007/s100380050154.

Abstract

We report the chromosomal localization of the gene for human poly(A) polymerase (PAP) and the characterization of a newly isolated CA repeat near the PAP locus. By fluorescence in situ hybridization and polymerase chain reaction (PCR)-based analysis with both a human/rodent monochromosomal hybrid cell panel and a radiation hybrid mapping panel, this gene was mapped on the q32.1-q32.2 region of chromosome 14. From a genomic clone containing the human PAP locus, we have isolated a polymorphic dinucleotide (CA) sequence. High heterozygosity (0.81) makes this polymorphism a useful marker in the genetic study of disorders localized at the 14q32 region, such as autosomal recessive congenital microphthalmia (CMIC).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping*
  • Chromosomes, Human, Pair 14*
  • Dinucleotide Repeats*
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Physical Chromosome Mapping
  • Polymorphism, Genetic*
  • Polynucleotide Adenylyltransferase / genetics*

Substances

  • Genetic Markers
  • Polynucleotide Adenylyltransferase

Associated data

  • GENBANK/AB025574