Ding Martina G, Butler Christine A, Saracco Scott A, Fox Thomas D, Godard François, di Rago Jean-Paul, Trumpower Bernard L
Department of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.
Biochim Biophys Acta. 2008 Sep;1777(9):1147-56. doi: 10.1016/j.bbabio.2008.04.029. Epub 2008 Apr 27.
We have previously used inhibitors interacting with the Qn site of the yeast cytochrome bc(1) complex to obtain yeast strains with resistance-conferring mutations in cytochrome b as a means to investigate the effects of amino acid substitutions on Qn site enzymatic activity [M.G. Ding, J.-P. di Rago, B.L. Trumpower, Investigating the Qn site of the cytochrome bc1 complex in Saccharomyces cerevisiae with mutants resistant to ilicicolin H, a novel Qn site inhibitor, J. Biol. Chem. 281 (2006) 36036-36043.]. Although the screening produced various interesting cytochrome b mutations, it depends on the availability of inhibitors and can only reveal a very limited number of mutations. Furthermore, mutations leading to a respiratory deficient phenotype remain undetected. We therefore devised an approach where any type of mutation can be efficiently introduced in the cytochrome b gene. In this method ARG8, a gene that is normally encoded by nuclear DNA, replaces the naturally occurring mitochondrial cytochrome b gene, resulting in ARG8 expressed from the mitochondrial genome (ARG8(m)). Subsequently replacing ARG8(m) with mutated versions of cytochrome b results in arginine auxotrophy. Respiratory competent cytochrome b mutants can be selected directly by virtue of their ability to restore growth on non-fermentable substrates. If the mutated cytochrome b is non-functional, the presence of the COX2 respiratory gene marker on the mitochondrial transforming plasmid enables screening for cytochrome b mutants with a stringent respiratory deficiency (mit(-)). With this system, we created eight different yeast strains containing point mutations at three different codons in cytochrome b affecting center N. In addition, we created three point mutations affecting arginine 79 in center P. This is the first time mutations have been created for three of the loci presented here, and nine of the resulting mutants have never been described before.
我们之前使用与酵母细胞色素bc(1)复合物的Qn位点相互作用的抑制剂,来获得细胞色素b中具有赋予抗性突变的酵母菌株,以此作为研究氨基酸取代对Qn位点酶活性影响的一种手段[M.G.丁,J.-P.迪拉戈,B.L.特朗普沃尔,用对新型Qn位点抑制剂伊利西考林H具有抗性的突变体研究酿酒酵母中细胞色素bc1复合物的Qn位点,《生物化学杂志》281 (2006) 36036 - 36043]。尽管筛选产生了各种有趣的细胞色素b突变,但它依赖于抑制剂的可用性,并且只能揭示非常有限数量的突变。此外,导致呼吸缺陷表型的突变仍未被检测到。因此,我们设计了一种方法,可以在细胞色素b基因中高效引入任何类型的突变。在这种方法中,通常由核DNA编码的基因ARG8取代天然存在的线粒体细胞色素b基因,导致从线粒体基因组表达的ARG8(ARG8(m))。随后用细胞色素b的突变版本取代ARG8(m)会导致精氨酸营养缺陷。具有呼吸能力的细胞色素b突变体可以直接根据它们在非发酵底物上恢复生长的能力来选择。如果突变的细胞色素b无功能,线粒体转化质粒上COX2呼吸基因标记的存在能够筛选出具有严格呼吸缺陷(mit(-))的细胞色素b突变体。利用这个系统,我们创建了八个不同的酵母菌株,它们在细胞色素b中影响中心N的三个不同密码子处含有点突变。此外,我们创建了三个影响中心P中精氨酸79的点突变。这是首次针对此处呈现的三个位点产生突变,并且所产生的九个突变体中有九个之前从未被描述过。