Orkin S H
J Biol Chem. 1977 Aug 25;252(16):5606-8.
A DNA probe specific for sequences complementary to globin RNA has been prepared in vitro from globin complementary DNA (cDNA). Globin cDNA was used as the template for the synthesis of a complementary strand (ccDNA) by avian myeloblastosis virus DNA polymerase. After treatment with single strand-specific S1 nuclease, double-stranded globin DNA was denatured in the presence of a vast excess of globin RNA. After hybridization of the cDNA with globin RNA, the ccDNA was isolated by hydroxyapatite chromatography. The ccDNA probe hybridized efficiently to globin cDNA, but not at all to globin RNA. This probe should prove useful in assessing the asymmetry of gene expression in cell-free transcriptional systems.
一种与珠蛋白RNA互补序列特异的DNA探针已在体外由珠蛋白互补DNA(cDNA)制备而成。珠蛋白cDNA被用作模板,通过禽成髓细胞瘤病毒DNA聚合酶合成互补链(ccDNA)。用单链特异性S1核酸酶处理后,双链珠蛋白DNA在大量过量的珠蛋白RNA存在下变性。cDNA与珠蛋白RNA杂交后,通过羟基磷灰石柱层析分离出ccDNA。该ccDNA探针能有效地与珠蛋白cDNA杂交,但与珠蛋白RNA完全不杂交。这种探针在评估无细胞转录系统中基因表达的不对称性方面应会证明是有用的。