Schenborn E T, Mierendorf R C
Nucleic Acids Res. 1985 Sep 11;13(17):6223-36. doi: 10.1093/nar/13.17.6223.
The in vitro synthesis of extraneous RNA sequences by SP6 and T7 RNA polymerases from specific DNA templates is described. Transcription of templates prepared by digestion with restriction enzymes that leave 3' protruding ends resulted in the production of significant amounts of long, template-sized RNA transcripts which hybridized to vector DNA. Sequences copied from the noncoding template strand were among the extraneous transcripts. The presence of these sequences in probe preparations were detected in Southern and RNase protection hybridization assays. In contrast, transcription of DNA templates with blunt or 5' protruding ends yielded few RNA products as extraneous sequences.
描述了通过SP6和T7 RNA聚合酶从特定DNA模板体外合成无关RNA序列的过程。用产生3'突出末端的限制性内切酶消化制备的模板进行转录,导致产生大量与载体DNA杂交的长的、模板大小的RNA转录本。从非编码模板链复制的序列存在于这些无关转录本中。在Southern杂交和RNA酶保护杂交试验中检测到探针制剂中存在这些序列。相比之下,具有平端或5'突出末端的DNA模板转录产生的作为无关序列的RNA产物很少。