Cech T R, Rio D C
Proc Natl Acad Sci U S A. 1979 Oct;76(10):5051-5. doi: 10.1073/pnas.76.10.5051.
R-loop hybridization and electron microscopy were used to map the RNA transcription products of the extrachromosomal rRNA genes of Tetrahymena thermophila. The mature 17S and 26S rRNAs and the nuclear 35S pre-rRNA and pre-26S rRNA were located with a precision of approximately 100 base pairs. A 370-base pair intervening sequence was found in the 26S coding region. It has the same size and relative location as that found in Tetrahymena pigmentosa [Wild, M.A. & Gall, J.G. (1979) Cell 16, 565-573]. One class of R-loop structures formed by nuclear pre-rRNA provided preliminary evidence for a primary transcript that contains the intervening sequence. The results suggested a processing scheme in which splicing of the intervening sequences is followed by a series of strand cleavages to give the mature 17S and 26S rRNAs. Analysis of the data also showed that RNA . DNA and DNA . DNA duplexes, when mounted for electron microscopy by the R-loop procedure, have the same length per base pair within 4%.
运用R环杂交和电子显微镜技术对嗜热四膜虫染色体外rRNA基因的RNA转录产物进行定位。成熟的17S和26S rRNA以及核内35S前体rRNA和前体26S rRNA的定位精度约为100个碱基对。在26S编码区发现了一段370个碱基对的间隔序列。其大小和相对位置与在色素四膜虫中发现的相同[怀尔德,M.A. & 高尔,J.G.(1979年)《细胞》16卷,565 - 573页]。由核内前体rRNA形成的一类R环结构为包含间隔序列的初级转录本提供了初步证据。结果提示了一种加工模式,即间隔序列剪接后接着进行一系列链切割,从而产生成熟的17S和26S rRNA。对数据的分析还表明,当通过R环程序制备用于电子显微镜观察时,RNA·DNA和DNA·DNA双链体每碱基对的长度在4%的范围内相同。