Goursot R, Mangin M, Bernardi G
EMBO J. 1982;1(6):705-11. doi: 10.1002/j.1460-2075.1982.tb01234.x.
We have investigated the mitochondrial genome of eight ori-zero spontaneous petite mutants of Saccharomyces cerevisiae. The tandem repeat units of these genomes do not contain any of the seven canonical ori sequences of the wild-type genome. Instead, they contain one, or more, ori-S sequences. These 44-nucleotide long surrogate origins of replication are a subset of GC clusters characterized by a potential secondary fold with two sequences ATAG and GGAG , inserted in AT spacers, two AT base pairs just following them, a GC stem (broken in the middle, and, in most cases also near the base, by non-paired nucleotides), and a terminal loop. This structure is reminiscent of that of GC clusters A and B from canonical ori sequences and supports the view (Bernardi, 1982a ) that the GC clusters of the mitochondrial genome arose, by an expansion process, from the canonical ori sequences. Like the latter, ori-S sequences are present in both orientations, are located in intergenic regions, and can be used as excision sequences when tandemly oriented. Again as in the case of canonical ori sequences, the density of ori-S sequences on the repeat units of petite genomes are correlated with the replication efficiency of the latter, as assessed by the outcome of crosses with wild-type or petite tester strains.
我们研究了酿酒酵母的八个ori-zero自发小菌落突变体的线粒体基因组。这些基因组的串联重复单元不包含野生型基因组的七个典型ori序列中的任何一个。相反,它们包含一个或多个ori-S序列。这些44个核苷酸长的替代复制起点是GC簇的一个子集,其特征是具有潜在的二级折叠,带有两个序列ATAG和GGAG,插入在AT间隔区中,紧接着它们有两个AT碱基对,一个GC茎(在中间断裂,并且在大多数情况下在碱基附近也被未配对的核苷酸打断),以及一个末端环。这种结构让人联想到典型ori序列中的GC簇A和B的结构,并支持这样一种观点(Bernardi,1982a),即线粒体基因组的GC簇是通过扩展过程从典型ori序列产生的。与典型ori序列一样,ori-S序列以两种方向存在,位于基因间区域,并且当串联排列时可以用作切除序列。同样与典型ori序列的情况一样,小菌落基因组重复单元上ori-S序列的密度与后者的复制效率相关,这通过与野生型或小菌落测试菌株杂交的结果来评估。