Lang K M, Spritz R A
Gene. 1985;33(2):191-6. doi: 10.1016/0378-1119(85)90093-9.
A simple method for extending partial cDNA clones of specific mRNA molecules is described. The method combines plasmid-primed first-strand cDNA synthesis [Okayama and Berg, Mol. Cell. Biol. 2 (1982) 161-170] with second-strand synthesis by primer extension. This approach selects for the synthesis of specific double-stranded cDNAs with complete 3' termini and poly(A) tails. We have used this method to extend preexisting cDNA clones to isolate 3' segments of human beta- and G gamma-globin cDNAs. These recombinants are particularly useful for the construction of templates for in vitro transcription of synthetic polyadenylylated mRNAs and pre-mRNAs. In addition, nucleotide sequence analysis of the cloned gamma-globin cDNA segment defined a previously unreported sequence polymorphism in the 3' untranslated region.
本文描述了一种扩展特定mRNA分子部分cDNA克隆的简单方法。该方法将质粒引发的第一链cDNA合成[冈山县和伯格,《分子细胞生物学》2(1982)161 - 170]与通过引物延伸进行的第二链合成相结合。这种方法可选择合成具有完整3'末端和poly(A)尾的特定双链cDNA。我们已使用此方法扩展现有的cDNA克隆,以分离人β-和Gγ-珠蛋白cDNA的3'片段。这些重组体对于构建用于体外转录合成聚腺苷酸化mRNA和前体mRNA的模板特别有用。此外,对克隆的γ-珠蛋白cDNA片段的核苷酸序列分析确定了3'非翻译区中一个以前未报道的序列多态性。