Clark-Walker G D, Azad A A
Nucleic Acids Res. 1980 Mar 11;8(5):1009-22. doi: 10.1093/nar/8.5.1009.
We have shown that 2.8 and 3.1 micron circular DNA molecules, previously reported to be present in Saccharomyces cerevisiae and Torulopsis glabrata respectively, contain sequences hybridizing to cytoplasmic ribosomal RNAs. In S. cerevisiae the 2.8 micron circular DNA appears to be identical to the rDNA repeating unit from nuclear DNA, both in length (approximately 9000 base pairs) and in the location of the 25, 18 and 5.8S rRNA sequences on the large HindIII fragment (6500 bp) and the presence of the 5S rRNA sequence on the small HindIII fragment. The 3.1 micron molecule from T. glabrata is approximately 2000 base pairs longer than the S. cerevisiae molecule and in addition, one of the HindIII sites lies within the region hybridizing to 25, 18 and 5.8S rRNAs. In S. cerevisiae the 4-5 copies of the 2.8 micron circular DNA molecules per cell, which have an extra-nuclear location, do not appear to be essential for cell viability as in one strain they were undetectable.
我们已经表明,先前分别报道存在于酿酒酵母和光滑球拟酵母中的2.8微米和3.1微米环状DNA分子,含有与细胞质核糖体RNA杂交的序列。在酿酒酵母中,2.8微米环状DNA在长度(约9000个碱基对)以及大HindIII片段(6500 bp)上25、18和5.8S rRNA序列的位置以及小HindIII片段上5S rRNA序列的存在方面,似乎与来自核DNA的rDNA重复单元相同。来自光滑球拟酵母的3.1微米分子比酿酒酵母分子长约2000个碱基对,此外,其中一个HindIII位点位于与25、18和5.8S rRNAs杂交的区域内。在酿酒酵母中,每个细胞中4 - 5个拷贝的2.8微米环状DNA分子位于核外,对于细胞活力似乎并非必不可少,因为在一个菌株中无法检测到它们。