MITOCHONDRIAL THEORY OF SENESCENCE - RESPIRATORY-CHAIN PROTEIN STUDIES IN HUMAN SKELETAL-MUSCLE

被引:24
作者
BYRNE, E [1 ]
TROUNCE, I [1 ]
DENNETT, X [1 ]
机构
[1] UNIV MELBOURNE,DEPT STATE NEUROPATHOL SERV,PARKVILLE,VIC 3052,AUSTRALIA
关键词
HUMAN MUSCLE MITOCHONDRIA; RESPIRATORY COMPLEX PROTEIN COMPOSITION; AGING;
D O I
10.1016/0047-6374(91)90042-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In view of a previously demonstrated negative correlation between stage III respiratory activity in human mitochondria and increasing age, the relationship between human respiratory chain complex protein content and age was investigated. Quantitative immunoblot studies were carried out using holo complex I, III and IV antibody probes in human skeletal muscle mitochondrial homogenate from patients of varying ages. No significant negative correlation between increased age and respiratory complex chain protein content was seen for either total complex activity or for any of the subunits which could be reliably identified. As respiratory complex protein content is preserved with ageing, the decrease in respiratory efficiency is likely to follow aggregation of mutations in structural mitochondrial (mt) DNA genes which do not interfere with mt DNA transcription and protein translation rather than mutations in mt tRNA or ribosomal RNA genes. This is consistent with the fact that mt genes involved in protein translation only occupy a fairly small percentage of the mitochondrial genome.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 13 条
[1]   PROGRESSION FROM MERRF TO MELAS PHENOTYPE IN A PATIENT WITH COMBINED RESPIRATORY COMPLEX-I AND COMPLEX-IV DEFICIENCIES [J].
BYRNE, E ;
TROUNCE, I ;
DENNETT, X ;
GILLIGAN, B ;
MORLEY, JB ;
MARZUKI, S .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1988, 88 (1-3) :327-337
[2]  
BYRNE E, 1990, Current Opinion in Rheumatology, V2, P889
[3]  
CARDELLACH F, 1989, LANCET, V2, P44
[4]   ENZYME-ACTIVITIES, GENE FUNCTION AND AGING IN MAMMALS - (REVIEW) [J].
FINCH, CE .
EXPERIMENTAL GERONTOLOGY, 1972, 7 (01) :53-+
[5]   IS CELL AGING CAUSED BY RESPIRATION-DEPENDENT INJURY TO THE MITOCHONDRIAL GENOME [J].
FLEMING, JE ;
MIQUEL, J ;
COTTRELL, SF ;
YENGOYAN, LS ;
ECONOMOS, AC .
GERONTOLOGY, 1982, 28 (01) :44-53
[6]   DELETIONS OF MUSCLE MITOCHONDRIAL-DNA IN PATIENTS WITH MITOCHONDRIAL MYOPATHIES [J].
HOLT, IJ ;
HARDING, AE ;
MORGANHUGHES, JA .
NATURE, 1988, 331 (6158) :717-719
[7]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[8]  
MARZUKI S, IN PRESS PROGR NEURO, V7
[9]   STUDIES OF SEQUENCE HETEROGENEITY OF MITOCHONDRIAL-DNA FROM RAT AND MOUSE-TISSUES - EVIDENCE FOR AN INCREASED FREQUENCY OF DELETIONS-ADDITIONS WITH AGING [J].
PIKO, L ;
HOUGHAM, AJ ;
BULPITT, KJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 1988, 43 (03) :279-293
[10]   MYOCLONIC EPILEPSY AND RAGGED-RED FIBER DISEASE (MERRF) IS ASSOCIATED WITH A MITOCHONDRIAL-DNA TRANSFER RNALYS MUTATION [J].
SHOFFNER, JM ;
LOTT, MT ;
LEZZA, AMS ;
SEIBEL, P ;
BALLINGER, SW ;
WALLACE, DC .
CELL, 1990, 61 (06) :931-937