Sequence Variations in the 5’ Hypersensitive Site-2 of the Locus Control Region of βsChromosomes Are Associated With Different Levels of Fetal Globin in Hemoglobin S Homozygotes

We have compared the sequence of the 5’ hypersensitive site-2 (5‘ ‘HS-2) of the locus control region (LCR) from a sickle cell anemia (SS) patient homozygous for haplotype 19 and with low levels of fetal hemoglobin (HbF), with the same sequence from an SS patient homozygous for haplotype 3 and with high levels of HbF. Several nucleotide variations were present in the 5’HS-2 of the haplotype 19 individual. One is the A → G at position -10905 that creates an Sp1 binding site GCCCC (A → GJCCCC. A second is the T G at position -10924 in a sequence that binds both erythroid and ubiquitous factors and exhibits high homology to the long terminal repeat of the Moloney leukemia viruses and Friend murine leukemia virus. Other differences were in the two AT-rich stretches of DNA, and an A →T substitution at position -10390. Dot-blot analyses of amplified DNA from several SS patients showed that these variations are specific for βs chromosomes with haplotype 19. We also examined the 5’HS-2 sequence from an SS patient who is homozygous for haplotype 19, but has abnormally high levels of HbF (>20%). We observed a cross-over that has placed sequences similar to the 5’HS-2 of haplotype 3 in juxtaposition to the 5’ flanking regions of haplotype 19. Thus, a βs chromosome with haplotype 19 but having a 5’HS-2 (LCR) characteristic for haplotype 3 is associated with high γ-chain expression. We postulate that factors produced under conditions of hematopoietic stress, together with genetic determinants on the haplotype 3-like LCR sequences, allow for high level expression of γ-globin genes.© 1992 by The American Society of Hematology. 0006-4971/92/7903-0024$3.00/0