Chromosomal localization of the human histone H2A.X gene to 11q23.2-q23.3 by fluorescence in situ hybridization

Hum Genet. 1994 Sep;94(3):303-6. doi: 10.1007/BF00208289.

Abstract

The human histone H2A.X gene is unusual in that its transcripts are alternatively processed to yield two species, one a 0.6-kb replication-linked histone mRNA and the other a 1.6-kb polyadenylated mRNA. The H2A.X gene has been localized by fluorescence in situ hybridization to chromosome 11q23.2-q23.3, away from the known clusters of human histone genes on chromosomes 1, 6, and 12. Assignment to chromosome 11 was substantiated by analysis of human-hamster somatic cell hybrid lines. As this work was being completed, an 89-bps sequence overlap was found between the downstream regions of the H2A.X gene and the recently sequenced hydroxymethylbilane (HMB)-synthase gene. The H2A.X and HMB-synthase genes have an unusual arrangement, being transcribed towards each other with their polyadenylation sites 330 bp apart. In addition the HMB-synthase gene contains constitutive and erythroid specific promoters. K562, an erythroid cell line, was found to contain a high concentration of the 1.6-kb polyadenylated H2A.X mRNA.

MeSH terms

  • Animals
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 11*
  • Cricetinae
  • Electrophoresis, Agar Gel
  • HeLa Cells
  • Histones / genetics*
  • Humans
  • Hybrid Cells
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • RNA, Messenger / analysis
  • Uroporphyrinogens / genetics

Substances

  • Histones
  • Oligonucleotide Probes
  • RNA, Messenger
  • Uroporphyrinogens
  • hydroxymethylbilane

Associated data

  • GENBANK/M95623