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The relative levels of β A and β S mRNAs in Hb S heterozygotes and in patients with Hb S‐β + ‐thalassaemia or Hb S‐β + ‐HPFH combinations
Author(s) -
Dimovski A. J.,
Efremov D. G.,
Gu LH.,
Huisman T. H. J.
Publication year - 1994
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1994.tb04921.x
Subject(s) - microbiology and biotechnology , heterozygote advantage , hemoglobinopathy , compound heterozygosity , fetal hemoglobin , messenger rna , loss of heterozygosity , thalassemia , gene expression , gene , biology , genetics , fetus , genotype , hemolytic anemia , allele , immunology , pregnancy
SUMMARY. We have used a quantitative reverse transcription/ polymerase chain reaction (RT/PCR) procedure to evaluate the relative amounts of β A and β S mRNA transcripts in eight subjects with a simple Hb S heterozygosity, in six with Hb S‐ β + ‐thalassaemia (thal), and in three individuals with Hb S‐ β + ‐HPFH [hereditary persistence of fetal haemoglobin (Hb)] [two with the Atlanta type and one with the G γ‐202 (C ± G) substitution]. A balanced synthesis of β A and β S mRNAs was observed in all Hb S heterozygotes, whereas the β A mRNA levels were reduced to ˜ 16% of that of the β S mRNA in the six Hb S‐ β + ‐thal compound heterozygotes, to ˜43% in the two subjects with Hb S‐ β + ‐HPFH (Atlanta type), and to 23.8% in the one individual with Hb S‐ β + ‐HPFH [ G γ‐202 (C ± G) substitution]. The higher Hb A versus Hb S levels observed in all groups of the patients studied, further confirm a post‐translational control mechanism in determining the levels of Hb A and Hb S in the peripheral blood of these individuals. The procedure described here provides an accurate and easy method for studying the relative expression of particular globin genes at the transcriptional level in patients with various haemoglobinopathies.