Temple G F, Chang J C, Kan Y W
Proc Natl Acad Sci U S A. 1977 Jul;74(7):3047-51. doi: 10.1073/pnas.74.7.3047.
In a patient with homozygous betaO-thalassemia in whom studies of reticulocyte hemoglobin synthesis showed no beta-globin chain synthesis in vivo and in vitro, molecular hybridization studies revealed RNA sequences complementary to beta-globin cDNA. The fact that these sequences were authentic beta-globin mRNA was shown by fingerprint analysis of T1 ribonuclease-digested mRNA and by sequencing of oligonucleotides unique to beta-globin mRNA. The beta-mRNA that failed to direct beta-globin chain synthesis was not detectably shortened or degraded and contained poly(A) sequences.
在一名纯合子β⁰-地中海贫血患者中,对网织红细胞血红蛋白合成的研究显示,体内和体外均无β-珠蛋白链合成,分子杂交研究揭示了与β-珠蛋白cDNA互补的RNA序列。通过对T1核糖核酸酶消化的mRNA进行指纹分析以及对β-珠蛋白mRNA特有的寡核苷酸进行测序,表明这些序列是真实的β-珠蛋白mRNA。未能指导β-珠蛋白链合成的β-mRNA未检测到明显缩短或降解,并且含有多聚腺苷酸序列。