Defects in DNA and globin messenger RNA in homozygotes for hemoglobin Lepore.

نویسندگان

  • F Ramirez
  • J G Mears
  • U Nudel
  • A Bank
  • L Luzzatto
  • G DiPrisco
  • R D'Avino
  • G Pepe
  • L Camardella
  • R Gambino
  • R Cimino
  • N Quattrin
چکیده

Globin messenger RNA (mRNA) isolated from three patients homozygous for hemoglobin Lepore is shown to have a marked reduction of the amount of beta-like globin mRNA (Lepore-globin mRNA sequences) compared with alpha-globin mRNA by molecular hybridization. The relative amounts of alpha- and Lepore mRNA are similar to the amounts of alpha- and Lepore globin synthesized in intact cells and by isolated mRNA in a cell-free system. It is also demonstrated that Lepore-globin mRNA can completely hybridize to full-length or nearly full-length beta-globin specific complementary DNA and protect it from nuclease digestion, indicating close homology between the delta-mRNA sequences present in Lepore mRNA and the beta-complementary-DNA probe. We have also quantitated the numbers of beta-like globin gene sequences in genomic Lepore DNA by molecular hybridization and demonstrated a reduction in their number consistent with the Lepore gene being a delta beta-gene fusion product.

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عنوان ژورنال:
  • The Journal of clinical investigation

دوره 63 4  شماره 

صفحات  -

تاریخ انتشار 1979