Ohta K, Nicolas A, Keszenman-Pereyra D, Shibata T
Laboratory of Cellular and Molecular Biology, Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.
Mol Gen Genet. 1996 Mar 7;250(4):395-404. doi: 10.1007/BF02174027.
Site-specific endonucleases have been found in various eukaryotic organelles such as mitochondria, chloroplasts and nuclei. These endonucleases initiate site-specific or homologous gene conversion in mitochondrial and nuclear DNA. Here, we report a new site-specific endonuclease activity, Endo.SK1, identified in mitochondria of strain SK1, a homothallic diploid strain of Saccharomyces cerevisiae. Nucleotide sequences around the Endo.SK1-cleavage sites are different from those of known yeast site-specific endonucleases. The Endo.SK1 activity is, at least partly, specified by a gene in the SK1-derived mitochondria. A novel feature of the Endo.SK1 activity is its inducibility: the endonuclease activity was induced by ca. 40-fold by transfer of cells from a glucose medium into an acetate medium, and was then repressed. This transient induction was independent of the ploidy level of the cells, and coincided with induction of fumarase, a mitochondrial enzyme involved in the TCA cycle. Co-induction and co-repression of the mitochondrial site-specific endonuclease activity and a respiration-related enzyme indicate that the endonuclease activity in regulated in response to physiological conditions, and suggest a possible role for the endonuclease in mitochondrial DNA metabolism.
位点特异性核酸内切酶已在各种真核细胞器中被发现,如线粒体、叶绿体和细胞核。这些核酸内切酶在线粒体和核DNA中引发位点特异性或同源基因转换。在此,我们报告了一种新的位点特异性核酸内切酶活性,Endo.SK1,它是在酿酒酵母同宗配合二倍体菌株SK1的线粒体中鉴定出来的。Endo.SK1切割位点周围的核苷酸序列与已知酵母位点特异性核酸内切酶的不同。Endo.SK1活性至少部分由SK1来源的线粒体中的一个基因决定。Endo.SK1活性的一个新特点是其可诱导性:当细胞从葡萄糖培养基转移到乙酸盐培养基中时,核酸内切酶活性被诱导约40倍,然后被抑制。这种短暂的诱导与细胞的倍性水平无关,并且与延胡索酸酶的诱导同时发生,延胡索酸酶是参与三羧酸循环的一种线粒体酶。线粒体位点特异性核酸内切酶活性与一种呼吸相关酶的共同诱导和共同抑制表明,核酸内切酶活性是根据生理条件进行调节的,并提示该核酸内切酶在线粒体DNA代谢中可能发挥作用。