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莱茵衣藻线粒体复合体I缺陷型突变体:影响nd1编码序列的两个突变的特征分析

Mutants of Chlamydomonas reinhardtii deficient in mitochondrial complex I: characterization of two mutations affecting the nd1 coding sequence.

作者信息

Remacle C, Baurain D, Cardol P, Matagne R F

机构信息

Laboratory of Genetics of Microorganisms, Department of Plant Biology, University of Liège, B-4000 Liège Sart-Tilman, Belgium.

出版信息

Genetics. 2001 Jul;158(3):1051-60. doi: 10.1093/genetics/158.3.1051.

Abstract

The mitochondrial rotenone-sensitive NADH:ubiquinone oxidoreductase (complex I) comprises more than 30 subunits, the majority of which are encoded by the nucleus. In Chlamydomonas reinhardtii, only five components of complex I are coded for by mitochondrial genes. Three mutants deprived of complex I activity and displaying slow growth in the dark were isolated after mutagenic treatment with acriflavine. A genetical analysis demonstrated that two mutations (dum20 and dum25) affect the mitochondrial genome whereas the third mutation (dn26) is of nuclear origin. Recombinational analyses showed that dum20 and dum25 are closely linked on the genetic map of the mitochondrial genome and could affect the nd1 gene. A sequencing analysis confirmed this conclusion: dum20 is a deletion of one T at codon 243 of nd1; dum25 corresponds to a 6-bp deletion that eliminates two amino acids located in a very conserved hydrophilic segment of the protein.

摘要

线粒体鱼藤酮敏感的NADH:泛醌氧化还原酶(复合体I)由30多个亚基组成,其中大多数由细胞核编码。在莱茵衣藻中,复合体I只有五个组分由线粒体基因编码。在用吖啶黄素进行诱变处理后,分离出了三个缺乏复合体I活性且在黑暗中生长缓慢的突变体。遗传学分析表明,两个突变(dum20和dum25)影响线粒体基因组,而第三个突变(dn26)起源于细胞核。重组分析表明,dum20和dum25在线粒体基因组的遗传图谱上紧密连锁,可能影响nd1基因。测序分析证实了这一结论:dum20是nd1基因第243位密码子处的一个T缺失;dum25对应于一个6个碱基对的缺失,该缺失消除了位于该蛋白质非常保守的亲水片段中的两个氨基酸。

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