Vs. Ivanova et al., CHROMOSOMAL LOCALIZATION OF THE HUMAN HISTONE H2A.X GENE TO 11Q23.2-Q23.3 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Human genetics, 94(3), 1994, pp. 303-306
The human histone H2A.X gene is unusual in that its transcripts are al
ternatively processed to yield two species, one a 0.6-kb replication-l
inked histone mRNA and the other a 1.6-kb polyadenylated mRNA. The H2A
.X gene has been localized by fluorescence in situ hybridization to ch
romosome 11q23.2-q23.3, away from the known clusters of human histone
genes on chromosomes 1, 6, and 12. Assignment to chromosome 11 was sub
stantiated by analysis of human-hamster somatic cell hybrid lines. As
this work was being completed, an 89-bps sequence overlap was found be
tween the downstream regions of the H2A.X gene and the recently sequen
ced hydroxymethylbilane (HMB)-synthase gene. The H2A.X and HMB-synthas
e genes have an unusual arrangement, being transcribed towards each ot
her 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 concentrati
on of the 1.6-kb polyadenylated H2A.X mRNA.