Cortese R, Harland R, Melton D
Proc Natl Acad Sci U S A. 1980 Jul;77(7):4147-51. doi: 10.1073/pnas.77.7.4147.
The expression of cloned tRNA genes has been studied by injecting single-stranded and double-stranded DNA templates into Xenopus oocyte nuclei. In both forms the genes are faithfully transcribed after injection. Some single-stranded DNA is converted into double-stranded DNA in the oocyte nucleus. This conversion is necessary for the expression of the injected tRNA gene: no tRNA transcription is observed when DNA synthesis is inhibited. We conclude that single-stranded DNA does not serve as a template for faithful transcription of this gene in injected oocytes.
通过将单链和双链DNA模板注射到非洲爪蟾卵母细胞核中,对克隆的tRNA基因的表达进行了研究。两种形式的基因在注射后都能被如实地转录。一些单链DNA在卵母细胞核中被转化为双链DNA。这种转化对于注射的tRNA基因的表达是必需的:当DNA合成受到抑制时,未观察到tRNA转录。我们得出结论,在注射的卵母细胞中,单链DNA不能作为该基因忠实转录的模板。