Kimura A, Matsunaga E, Takihara Y, Nakamura T, Takagi Y, Lin S, Lee H
J Biol Chem. 1983 Mar 10;258(5):2748-9.
The beta-globin gene from a patient with homozygous beta-thalassemia in Taiwan was cloned and extensively sequenced. Four nucleotides in the codon for amino acids, 41 and 42, are deleted. This change generates a frame-shift mutation and a termination codon in the new 59th codon. Some changes in nucleotide sequence were also found in intervening sequences IVS1 and IVS2, and Exon3, and were considered to be sequence polymorphisms.
克隆并全面测序了来自台湾一名纯合β地中海贫血患者的β珠蛋白基因。第41和42位氨基酸密码子中的四个核苷酸缺失。这一变化产生了一个移码突变,并在新的第59位密码子中产生了一个终止密码子。在内含子序列IVS1、IVS2和外显子3中也发现了核苷酸序列的一些变化,这些变化被认为是序列多态性。