Defects in DNA and globin messenger RNA in homozygotes for hemoglobin Lepore.
Open Access
- 1 April 1979
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 63 (4) , 736-742
- https://doi.org/10.1172/jci109357
Abstract
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.This publication has 39 references indexed in Scilit:
- Studies of Globin Chain Synthesis and Globin mRNA Content in a Patient Homozygous for Hemoglobin LeporeHemoglobin, 1978
- The rabbit β-globin gene contains a large insert in the coding sequenceCell, 1977
- Quantitation of human gamma globin genes and gamma globin mRNA with purified gamma globin complementary DNA.Journal of Clinical Investigation, 1976
- Abnormal or absent β mRNA in β0 Ferrara and gene deletion in δβ thalassaemiaNature, 1976
- δβ-Thalassemia is due to a gene deletionCell, 1976
- A direct estimate of the number of human γ-globin genesCell, 1976
- Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobinCell, 1976
- Deletion of the β-globin structure gene in hereditary persistence of foetal haemoglobinNature, 1975
- The synthesis of human haemoglobin A2 during erythroid maturationBiochemical and Biophysical Research Communications, 1972
- Studies on Hemoglobin Biosynthesis: Asynchronous Synthesis of Hemoglobin A and Hemoglobin A2 by Erythrocyte Precursors *Journal of Clinical Investigation, 1965