首页> 外文期刊>Biochimica et biophysica acta. Bioenergetics >Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size
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Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size

机译:线粒体呼吸速率和呼吸链复合物活性与缺失的mtDNA的杂种性呈线性相关,且无阈值,且与缺失大小无关

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To clarify the importance of deleted protein and tRNA genes on the impairment of mitochondrial function, we performed a quantitative analysis of biochemical, genetic and morphological findings in skeletal muscles of 16 patients with single deletions and 5 patients with multiple deletions of mtDNA. Clinically, all patients showed chronic progressive external ophthalmoplegia (CPEO). The size of deletions varied between 2.5 and 9 kb, and heteroplasmy between 31% and 94%. In patients with single deletions, the citrate (CS) activity was nearly doubled. Decreased ratios of pyruvate- and succinate-dependent respiration were detected in fibers of all patients in comparison to controls. Inverse and linear correlations without thresholds were established between heteroplasmy and (i) CS referenced activities of the complexes of respiratory chain, (ii) CS referenced maximal respiratory rates, (iii) and cytochrome-c-oxidase (COX) negative fibers. In patients with single and multiple deletions, all respiratory chain complexes as well as the respiratory rates were decreased to a similar extent. All changes detected in patients with single deletions were independent of deletion size. In one patient, only genes of ND5, ND4L as well as tRNA_(Leu(CUN)), tRNA_(Ser(AGY)), and tRNA_(His) were deleted. The pronounced decrease in COX activity in this patient points to the high pathological impact of these missing tRNA genes. The activity of nuclear encoded SDH was also significantly decreased in patients, but to a lesser extent. This is indication of secondary disturbances of mitochondria at CPEO. In conclusion, we have shown that different deletions cause mitochondrial impariments of the same phenotype correlating with heteroplasmy. The missing threshold at the level of mitochondrial function seems to be characteristic for large-scale deletions were tRNA and protein genes are deleted.
机译:为了阐明缺失的蛋白质和tRNA基因对线粒体功能受损的重要性,我们对16例单缺失的mtDNA和5例多重缺失的mtDNA的骨骼肌进行了生化,遗传和形态学发现的定量分析。临床上,所有患者均表现为慢性进行性眼外肌麻痹(CPEO)。缺失的大小在2.5到9 kb之间变化,异质性在31%到94%之间变化。在具有单一缺失的患者中,柠檬酸盐(CS)活性几乎翻倍。与对照组相比,在所有患者的纤维中检出的丙酮酸和琥珀酸依赖性呼吸比率均降低。异质性与(i)呼吸链复合物的CS参照活性,(ii)CS参照的最大呼吸频率,(iii)和细胞色素-c-氧化酶(COX)阴性纤维之间建立了没有阈值的反相关和线性相关性。在具有单个或多个缺失的患者中,所有呼吸链复合物以及呼吸频率均下降了相似的程度。单个缺失患者中检测到的所有变化均与缺失大小无关。在一名患者中,仅删除了ND5,ND4L以及tRNA_(Leu(CUN)),tRNA_(Ser(AGY))和tRNA_(His)的基因。该患者中COX活性的明显下降表明这些缺失的tRNA基因具有高度的病理学影响。患者中核编码的SDH的活性也显着降低,但程度较小。这表明在CPEO处线粒体的继发性紊乱。总之,我们已经表明,不同的缺失会导致与异质性相关的相同表型的线粒体障碍。线粒体功能水平的缺失阈值似乎是tRNA和蛋白基因被缺失时大规模缺失的特征。

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