Mitochondrial DNA mutations in RRF of healthy subjects of different age

被引:28
作者
Cormio, A
Milella, F
Vecchiet, J
Felzani, G
Gadaleta, MN
Cantatore, P
机构
[1] Univ Bari, Dipartmento Biochim & Biol Mol, I-70125 Bari, Italy
[2] Univ Chieti G Annunzio, Cattedra Malattie Infett, I-66013 Chieti, Italy
[3] Univ Chieti G Annunzio, Dipartimento Med Interna & Sci Invecchiamento, I-66013 Chieti, Italy
[4] CNR, Inst Biomembrane & Bioenerget, I-70125 Bari, Italy
[5] Univ Bari, Ctr Eccellenza Genom Comparata Campo Biomed & Agr, Dipartimento Farmacobiol, I-70125 Bari, Italy
关键词
human skeletal muscle; ragged red fibers; mtDNA; point mutations; aging;
D O I
10.1016/j.neurobiolaging.2004.06.014
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
To obtain information on the mechanisms responsible of the generation of ragged red fibers (RRF) during aging, we analyzed the mitochondrial genotype of single skeletal muscle fibers of healthy individuals having an age comprised between 45 and 92 years. The sequencing of the D-loop region showed many sequence changes with respect to the Cambridge reference sequence (CRS), in both RRF and normal fibers. These changes were more abundant in RRF and their number increased between 50 and 60, and 61 and 70 years and then remained approximately constant. The analysis of the sequence changes showed that each subject contained one or more changes associated to RRF in positions of D-loop region that either do not change or that change very rarely. In general the same type of RRF-associated change was not found in more than one individual; exceptions were changes in positions 189, 295, 374 and 514, detected in 20-50% of analyzed subjects. In particular the A189G age-associated mutation was found only in old individuals and prevalently in RRE Sequencing of other two mtDNA regions showed no relevant changes in the 16S/ND1 region and two RRF-associated original mutations, G5847A and A5884C, in two very conserved positions of tRNA(Tyr). These results indicate that each subject has its own pattern of RRF-associated mutations in both coding and non-coding region of human mtDNA. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:655 / 664
页数:10
相关论文
共 42 条
[1]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[2]   ANIMAL MITOCHONDRIAL-DNA - AN EXTREME EXAMPLE OF GENETIC ECONOMY [J].
ATTARDI, G .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1985, 93 :93-145
[3]   Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle [J].
Brierley, EJ ;
Johnson, MA ;
Lightowlers, RN ;
James, OFW ;
Turnbull, DM .
ANNALS OF NEUROLOGY, 1998, 43 (02) :217-223
[4]   PARTIAL CYTOCHROME-OXIDASE (AA3) DEFICIENCY IN CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA - HISTOCHEMICAL AND BIOCHEMICAL-STUDIES [J].
BYRNE, E ;
DENNETT, X ;
TROUNCE, I ;
HENDERSON, R .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1985, 71 (2-3) :257-271
[5]   ORGANIZATION, STRUCTURE, AND EVOLUTION OF MAMMALIAN MITOCHONDRIAL GENES [J].
CANTATORE, P ;
SACCONE, C .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1987, 108 :149-208
[6]   Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection [J].
Cao, ZJ ;
Wanagat, J ;
McKiernan, SH ;
Aiken, JM .
NUCLEIC ACIDS RESEARCH, 2001, 29 (21) :4502-4508
[7]   MtDNA mutations in aging and apoptosis [J].
Chomyn, A ;
Attardi, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (03) :519-529
[8]   MELAS MUTATION IN MTDNA BINDING-SITE FOR TRANSCRIPTION TERMINATION FACTOR CAUSES DEFECTS IN PROTEIN-SYNTHESIS AND IN RESPIRATION BUT NO CHANGE IN LEVELS OF UPSTREAM AND DOWNSTREAM MATURE TRANSCRIPTS [J].
CHOMYN, A ;
MARTINUZZI, A ;
YONEDA, M ;
DAGA, A ;
HURKO, O ;
JOHNS, D ;
LAI, ST ;
NONAKA, I ;
ANGELINI, C ;
ATTARDI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) :4221-4225
[9]   DETECTION OF A SPECIFIC MITOCHONDRIAL-DNA DELETION IN TISSUES OF OLDER HUMANS [J].
CORTOPASSI, GA ;
ARNHEIM, N .
NUCLEIC ACIDS RESEARCH, 1990, 18 (23) :6927-6933
[10]   Remarkable infidelity of polymerase γA associated with mutations in POLG1 exonuclease domain [J].
Del Bo, R ;
Bordoni, A ;
Sciacco, M ;
Di Fonzo, A ;
Galbiati, S ;
Crimi, M ;
Bresolin, N ;
Comi, GP .
NEUROLOGY, 2003, 61 (07) :903-908