GLOBIN MESSENGER-RNA IN BETA-THALASSEMIA HETEROZYGOTES WITH DIFFERENTBETA-THALASSEMIA ALLELES AND IN HETEROZYGOTES FOR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN

Reverse transcriptase-polymerase chain reaction (RT-PCR) was used to d etermine the alpha 2/alpha 1-, alpha/beta-, and gamma/beta-mRNA ratios in subjects with beta-thalassemia (beta-thal), hereditary persistence of fetal hemoglobin (HPFH), and normal adults. The alpha- and beta-gl obin gene mutations were characterized with gene mapping, PCR, and DNA sequencing. The average alpha 2/alpha 1-mRNA ratio was the same in no rmal adults and beta-thal heterozygotes with four alpha-globin genes ( 2.61-2.63) or with an alpha-thal-2 trait (1.48-1.55). The average alph a/beta-mRNA ratios were 4.47 and 3.84 in normal adults with four alpha -globin genes and with alpha-thal-2 trait (-alpha/alpha alpha), respec tively. There was an increase of similar to 50% in beta-thal heterozyg otes with transcriptional mutants [-88 (C --> T) and -29 (A --> G)] wi th lower values (similar to 25%) in those with alpha-thal-2 trait (-al pha/alpha). High alpha/beta ratios were also observed for heterozygote s for nonsense or frameshift mutants located in exon 1 or exon 2. Incr eases of similar to 150-165% were seen in subjects with RNA processing defects; an exception was the IVS-I-110 (G --> A) mutation with a nor mal value in the heterozygote. The increases were also less pronounced in heterozygotes for the codon (CD) 121 (G --> T) mutation and the CD s 134-137 insertion/deletion. Normal alpha/(gamma+beta) values were se en in 3 heterozygotes each with a different deletion involving part of the P-globin gene. The presence of the silent beta-thal allele, -101 (C --> T), in trans to a CD 8 (-AA) allele has a minor effect on the a lpha/beta-mRNA ratio. The alpha/beta-mRNA ratio in HPFH heterozygotes was similar to 145% of normal, but with a gamma-mRNA level of 35.4-44. 7% the calculated alpha/(gamma+beta) ratio became as in normal adults. The RT-PCR methodology appears useful in expression studies in beta-t hal (and HPFH) and values of mRNA appear to correspond to the type of prevailing mutation(s) and concomitant alpha-thai.