Extent and high frequency of a short conversion between the human A gamma and G gamma fetal globin genes

Hum Genet. 1990 Jan;84(2):179-84. doi: 10.1007/BF00208937.

Abstract

Southern blotting and DNA sequencing after polymerase chain reaction (PCR) amplification provide evidence for the frequent occurrence (in 7 out of 24 chromosomes) of a short conversion G gamma----A gamma in the 3' end of the human fetal A gamma globin gene. This short conversion is characterized by the presence, 3 nucleotides downstream from the termination codon of the A gamma gene, of the TCAC sequence that is normally present at the equivalent position at the 3' end of the G gamma gene; it is therefore identical to a conversion already described. Interestingly, we have found that this conversion is associated with the presence of the HindIII polymorphic restriction site in the A gamma IVS2, occupying an equivalent position in both the G gamma and A gamma genes. Our observations strengthen the hypothesis that the presence of the HindIII polymorphic restriction site in A gamma IVS2 and the presence of the sequence TCAC at the 3' end of the A gamma gene might be the result of a single conversion event.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Fetal Blood
  • Fetal Hemoglobin / genetics*
  • Gene Conversion*
  • Globins / genetics*
  • Humans
  • Infant, Newborn
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Restriction Mapping

Substances

  • Globins
  • Fetal Hemoglobin