早期区β -珠蛋白cDNA取代的SV40重组体的构建与鉴定

P J Southern, B H Howard, P Berg
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引用次数: 0

摘要

编码兔β -珠蛋白的cDNA片段被插入到猴病毒40 (SV40)早期区的不同位置。这些重组体中插入的序列是从SV40早期区域启动子转录而来的,初级转录本利用病毒干预序列和早期区域多聚腺苷化位点加工成成熟的mrna。多种重组体感染后,β -珠蛋白翻译起始密码子位于信使RNA序列的第一个AUG时,β -珠蛋白多肽才会合成。当早期转录本包含-珠蛋白cDNA序列3-邻小t抗原编码序列时,无法检测到-珠蛋白合成。然而,这些重组产生小t抗原和大t抗原的缩写形式。
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Construction and characterization of SV40 recombinants with beta-globin cDNA substitutions in their early regions.

A cDNA segment coding for rabbit beta-globin has been inserted at different locations in the early region of simian virus 40 (SV40). The inserted sequences in these recombinants are transcribed from the SV40 early region promoter, and the primary transcripts are processed to mature mRNAs using viral intervening sequences and the early region polyadenylation site. After infection with various recombinants, beta-globin polypeptide is synthesized only when the beta-globin translation initiation codon is the first AUG in the messenger RNA sequence. When the early region transcripts contain the beta-globin cDNA sequence 3-proximal to the small t antigen coding sequence, beta-globin synthesis is not detectable. However, these recombinants produce small t antigen and abbreviated forms of large T antigen.

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