Meyerink J H, Retèl J, Raué H A, Planta R J
Nucleic Acids Res. 1978 Aug;5(8):2801-8. doi: 10.1093/nar/5.8.2801.
The genetic organization of the multiple ribosomal transcription units (RTUs) on the genome of the yeast Saccharomyces carlsbergensis was studied by electron microscopy of purified ribosomal DNA hybridized to 26S rRNA using the R-loop technique (Thomas, M., White, R.L. and Davis, R.W. (1973) Proc. Natl. Acad. Sci. U.S. 73, 2294-2298). Plasmid pBR 322, the molecular weight of which is known, was used as a standard for converting contour length of double-stranded DNA into molecular weight. The 140 yeast RTUs were found to be arrayed in tandem repeats, each repeat containing at most 0.4 X 10(6) D (about 6% of the length of the RTU) of non-transcribed spacer DNA. The repeats, in turn, are arranged in a number of clusters separated by much longer stretches of non-ribosomal DNA.
利用R环技术(Thomas, M., White, R.L.和Davis, R.W.(1973年),《美国国家科学院院刊》73卷,2294 - 2298页),通过对与26S rRNA杂交的纯化核糖体DNA进行电子显微镜观察,研究了卡尔斯伯酵母基因组上多个核糖体转录单位(RTU)的基因组织。已知分子量的质粒pBR 322被用作将双链DNA的轮廓长度转换为分子量的标准。发现140个酵母RTU串联重复排列,每个重复最多包含0.4×10⁶D(约占RTU长度的6%)的非转录间隔DNA。这些重复序列又排列成许多簇,由长得多的非核糖体DNA片段隔开。