MUTATIONS AFFECTING THE MITOCHONDRIAL GENES ENCODING THE CYTOCHROME-OXIDASE SUBUNIT-I AND APOCYTOCHROME-B OF CHLAMYDOMONAS-REINHARDTII

被引:32
作者
COLIN, M
DORTHU, MP
DUBY, F
REMACLE, C
DINANT, M
WOLWERTZ, MR
DUYCKAERTS, C
SLUSE, F
MATAGNE, RF
机构
[1] UNIV LIEGE,DEPT BOT,B-4000 LIEGE,BELGIUM
[2] UNIV LIEGE,CTR INTERDISCIPLINAIRE BIOCHIM NORMALE & PATHOL O,B-4000 LIEGE,BELGIUM
来源
MOLECULAR & GENERAL GENETICS | 1995年 / 249卷 / 02期
关键词
CHLAMYDOMONAS; MITOCHONDRIAL GENETICS; CYTOCHROME C OXIDASE; APOCYTOCHROME B;
D O I
10.1007/BF00290364
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial mutants of the green alga Chlamydomonas reinhardtii that are inactivated in the cytochrome pathway of respiration have previously been isolated. Despite the fact that the alternative oxidase pathway is still active the mutants have lost the capacity to grow heterotrophically (dark + acetate) and display reduced growth under mixotrophic conditions (light + acetate). In crosses between wild-type and mutant cells, the meiotic progeny only inherit the character transmitted by the mt(-) parent, which indicates that the mutations are located in the 15.8 kb linear mitochondrial genome. Two new mutants (dum-18 and dum-19) have now been isolated and characterized genetically, biochemically and at the molecular level. In addition, two previously isolated mutants (dum-11 and dum-15) were characterized in more detail. dum-11 contains two types of deleted mitochondrial DNA molecules: 15.1 kb monomers lacking the subterminal part of the genome, downstream of codon 147 of the apocytochrome b (COB) gene, and dimers resulting from head-to-head fusion of asymmetrically deleted monomers (15.1 and 9.5 kb DNA molecules, respectively). As in the wild type, the three other mutants contain only 15.8 kb mitochondrial DNA molecules. dum-15 is mutated at codon 140 of the COB gene, a serine (TCT) being changed into a tyrosine (TAC). dum-18 and dum-19 both inactivate cytochrome c oxidase, as a result of frameshift mutations (addition or deletion of 1 bp) at codons 145 and 152, respectively, of the COX1 gene encoding subunit I of cytochrome c oxidase. In a total of ten respiratory deficient mitochondrial mutants characterized thus far, only mutations located in COB or COX1 have been isolated. The possibility that the inactivation of the other mitochondrial genes is lethal for the cells is discussed.
引用
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页码:179 / 184
页数:6
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