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DEFECTS IN DNA AND GLOBIN MESSENGER-RNA IN HOMOZYGOTES FOR HEMOGLOBIN LEPORE
被引:16
作者:
RAMIREZ, F
MEARS, JG
NUDEL, U
BANK, A
LUZZATTO, L
DIPRISCO, G
DAVINO, R
PEPE, G
CAMARDELLA, L
GAMBINO, R
CIMINO, R
QUATTRIN, N
机构:
[1] COLUMBIA UNIV,HLTH SCI CTR,DEPT HUMAN GENET,NEW YORK,NY 10032
[2] COLUMBIA UNIV,HLTH SCI CTR,DEPT DEV,NEW YORK,NY 10032
[3] OSPED CARDARELLI,SOCIAL CTR THALASSEMIA & GENOTYP HEMOGLOBINOPATH,NAPLES,ITALY
[4] INT INST GENET & BIOPHYS,MARCONI 10,NAPLES,ITALY
[5] ARCO FELICE,MOLEC EMBRIOL LAB,NAPLES,ITALY
[6] OSPED CARDARELLI,DEPT HEMATOL,NAPLES,ITALY
关键词:
D O I:
10.1172/JCI109357
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Globin messenger RNA (mRNA) isolated from 3 patients homozygous for hemoglobin Lepore is shown to have a marked reduction of the amount of β-like globin mRNA (Lepore-globin mRNA sequences) compared with α-globin mRNA by molecular hybridization. The relative amounts of α- and Lepore mRNA are similar to the amounts of α- 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 β-globin specific complementary DNA and protect it from nuclease digestion, indicating close homology between the δ-mRNA sequences present in Lepore mRNA and the β-complementary-DNA probe. The authors have also quantitated the numbers of β-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 δβ-gene fusion product.
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页码:736 / 742
页数:7
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