首页> 美国卫生研究院文献>The Journal of Clinical Investigation >New amber mutation in a beta-thalassemic gene with nonmeasurable levels of mutant messenger RNA in vivo.
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New amber mutation in a beta-thalassemic gene with nonmeasurable levels of mutant messenger RNA in vivo.

机译:β-地中海贫血基因中的新琥珀突变体内突变信使RNA的水平无法测量。

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摘要

We have identified a beta-thalassemia gene that carries a novel nonsense mutation in a Chinese patient. This mutation, a G to T substitution at the first position of codon 43, changes the glutamic acid coding triplet (GAG) to a terminator codon (TAG). Based on oligonucleotide hybridization studies of 78 Chinese and Southeast Asian beta-thalassemia chromosomes, we estimate that this mutation accounts for a small minority of the beta-thalassemia mutations in that population. Study of the expression of this cloned gene in a transient expression system demonstrated a 65% decrease in levels of normally spliced mutant beta-globin mRNA. However, the study of reticulocyte RNA isolated from an individual heterozygous for this mutation demonstrated a total absence of this mutant mRNA in vivo. The basis for this big discrepancy between the level of accumulated mRNA in vivo and in vitro is probably the result of differences in the stabilities of the mutant mRNA in erythroid cells.
机译:我们已经鉴定出在中国患者中携带新型无意义突变的β地中海贫血基因。这种突变是在第43个密码子的第一个位置进行了G到T取代,将谷氨酸编码三联体(GAG)更改为终止子密码子(TAG)。基于对78个中国和东南亚β-地中海贫血染色体的寡核苷酸杂交研究,我们估计该突变占该人群中β-地中海贫血突变的一小部分。在瞬时表达系统中对该克隆基因表达的研究表明,正常剪接的突变型β-珠蛋白mRNA的水平降低了65%。然而,从单个杂合子中分离出针对这种突变的网状细胞RNA的研究表明,该突变体在体内完全不存在。体内和体外积累的mRNA水平之间存在巨大差异的基础可能是突变型mRNA在红系细胞中稳定性差异的结果。

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