Multiple Defects in the Respiratory Chain Lead to the Repression of Genes Encoding Components of the Respiratory Chain and TCA Cycle Enzymes

被引:7
作者
Bourges, Ingrid [2 ]
Mucchielli, Marie-Helene [1 ,3 ]
Herbert, Christopher J. [1 ]
Guiard, Bernard [1 ]
Dujardin, Genevieve [1 ]
Meunier, Brigitte [1 ]
机构
[1] CNRS, Ctr Genet Mol, FRC 3115, F-91198 Gif Sur Yvette, France
[2] Univ Massachusetts, Sch Med, BMP, LRB, Worcester, MA 01605 USA
[3] Univ Paris 06, F-7500 Paris, France
关键词
yeast mutants; respiratory enzymes; gene expression; Hap2/3/4/5; respiratory dysfunction; CYTOCHROME-C-OXIDASE; SACCHAROMYCES-CEREVISIAE; MITOCHONDRIAL BIOGENESIS; MESSENGER-RNAS; YEAST; OXA1; MUTATIONS; COMPLEX; MORPHOLOGY; MEMBRANE;
D O I
10.1016/j.jmb.2009.02.039
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
Respiratory complexes III, IV and V are formed by components of both nuclear and mitochondrial origin and are embedded in the inner mitochondrial membrane. Their assembly requires the auxiliary factor Oxa1, and the absence of this protein has severe consequences on these three major respiratory. chain enzymes. We have studied, in the yeast Saccharomyces cerevisiae, the effect of the loss of Oxa1 function and of other respiratory defects on the expression of nuclear genes encoding components of the respiratory complexes and tricarboxylic acid cycle enzymes. We observed that the concomitant decrease in the level of two respiratory enzymes, complexes III and IV, led to their repression. These genes are known targets of the transcriptional activator complex Hap2/3/4/5 that plays a central role in the reprogramming of yeast metabolism when cells switch from a fermenting, glucose-repressed state to a respiring, derepressed state. We found that the Hap4 protein, the regulatory subunit of the transcriptional complex, was present at a lower level in the oxa1 mutants whereas no change in HAP4 transcript level was observed, suggesting a posttranscriptional modulation. In addition, an altered mitochondrial morphology was observed in mutants with decreased expression of Hap2/3/4/5 target genes. We suggest that the aberrant mitochondrial morphology, presumably caused by the severely decreased level of at least two respiratory enzymes, might be part of the signalling pathway linking the mitochondrial defect and Hap2/3/4/5. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1081 / 1091
页数:11
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