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β-地中海贫血由β-珠蛋白基因共有剪接受体序列中的两个新核苷酸替换所致。

Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene.

作者信息

Wong C, Antonarakis S E, Goff S C, Orkin S H, Forget B G, Nathan D G, Giardina P J, Kazazian H H

机构信息

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore.

出版信息

Blood. 1989 Mar;73(4):914-8.

PMID:2920213
Abstract

We have identified two novel RNA-splicing mutations affecting a critical nucleotide (nt) in the acceptor consensus sequences at both the IVS-1/exon 2 and IVS-2/exon 3 junctions of the human beta-globin gene. Both mutations are single nt substitutions, T to G and C to A, at position -3 adjacent to the invariant AG dinucleotide. For the IVS-2/exon 3 mutation abnormal splicing into the cryptic splice site at IVS-2 nt 579 is documented. Identification of these two mutations provides further support for the importance of the location of specific nucleotides within the consensus sequences in splice site selection and RNA processing.

摘要

我们已经鉴定出两个新的RNA剪接突变,它们影响人β-珠蛋白基因IVS-1/外显子2和IVS-2/外显子3连接处受体共有序列中的一个关键核苷酸(nt)。这两个突变都是单核苷酸替换,分别是在与不变的AG二核苷酸相邻的-3位置由T替换为G以及由C替换为A。对于IVS-2/外显子3突变,有文献记录了异常剪接进入IVS-2 nt 579处的隐蔽剪接位点。这两个突变的鉴定进一步支持了共有序列中特定核苷酸的位置在剪接位点选择和RNA加工中的重要性。

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