Missense mutation of the last nucleotide of exon 1 (G->C) of beta globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele.

نویسندگان

  • Neeraj Agarwal
  • Ferdane Kutlar
  • Mariluz P Mojica-Henshaw
  • Ching N Ou
  • Amos Gaikwad
  • N Scott Reading
  • Lakeia Bailey
  • Abdullah Kutlar
  • Josef T Prchal
چکیده

Hemoglobin Monroe (beta globin G->C, codon 30) is a missense mutation. We could not detect either the mutant peptide or transcript in reticulocyte-enriched preparation and in expanded erythroid progenitor cells. By quantitative gene expression assay beta globin mRNA was found to be reduced by more than 70% in all heterozygous subjects with different haplotypes. We conclude that this mutation also interferes with expression of wild type allele.

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عنوان ژورنال:
  • Haematologica

دوره 92 12  شماره 

صفحات  -

تاریخ انتشار 2007