Yamasaki Tomohito, Kurokawa Sayuri, Watanabe Kazuo I, Ikuta Kyosuke, Ohama Takeshi
Graduate School of Engineering, Department of Environmental Systems Engineering, Kochi University of Technology (KUT), Tosayamada, Kochi, Japan.
Plant Mol Biol. 2005 Jul;58(4):515-27. doi: 10.1007/s11103-005-7081-3.
Three types of respiratory deficient mitochondrial strains have been reported in Chlamydomonas reinhardtii: a deficiency due to (i) two base substitutions causing an amino acid change in the apocytochrome b (COB) gene (i.e., strain named dum-15), (ii) one base deletion in the COXI gene (dum-19), or (iii) a large deletion extending from the left terminus of the genome to somewhere in the COB gene (dum-1, -14, and -16). We found that these respiratory deficient strains of C. reinhardtii can be divided into two groups: strains that are constantly transformable and those could not be transformed in our experiments. All transformable mitochondrial strains were limited to the type that has a large deletion in the left arm of the genome. For these mitochondria, transformation was successful not only with purified intact mitochondrial genomes but also with DNA-constructs containing the compensating regions. In comparison, mitochondria of all the non-transformable strains have both of their genome termini intact, leading us to speculate that mitochondria lacking their left genome terminus have unstable genomes and might have a higher potential for recombination. Analysis of mitochondrial gene organization in the resulting respiratory active transformants was performed by DNA sequencing and restriction enzyme digestion. Such analysis showed that homologous recombination occurred at various regions between the mitochondrial genome and the artificial DNA-constructs. Further analysis by Southern hybridization showed that the wild-type genome rapidly replaces the respiratory deficient monomer and dimer mitochondrial genomes, while the E. coli vector region of the artificial DNA-construct likely does not remain in the mitochondria.
(i)由于两个碱基替换导致脱辅基细胞色素b(COB)基因中的氨基酸发生变化而产生的缺陷(即命名为dum - 15的菌株),(ii)COXI基因中的一个碱基缺失(dum - 19),或(iii)从基因组左端延伸至COB基因某处的大片段缺失(dum - 1、- 14和- 16)。我们发现,莱茵衣藻的这些呼吸缺陷型菌株可分为两组:持续可转化的菌株和在我们的实验中无法转化的菌株。所有可转化的线粒体菌株都局限于基因组左臂有大片段缺失的类型。对于这些线粒体,不仅用纯化的完整线粒体基因组,而且用含有补偿区域的DNA构建体都能成功实现转化。相比之下,所有不可转化菌株的线粒体基因组两端都是完整的,这使我们推测,缺乏基因组左端的线粒体基因组不稳定,可能具有更高的重组潜力。通过DNA测序和限制性内切酶消化对所得呼吸活性转化体中的线粒体基因组织进行了分析。这种分析表明,线粒体基因组与人工DNA构建体之间的各个区域都发生了同源重组。通过Southern杂交进一步分析表明,野生型基因组迅速取代了呼吸缺陷型单体和二聚体线粒体基因组,而人工DNA构建体的大肠杆菌载体区域可能不会保留在线粒体中。