PATIENTS WITH IDIOPATHIC CARDIOMYOPATHY BELONG TO THE SAME MITOCHONDRIAL-DNA GENE FAMILY OF PARKINSONS-DISEASE AND MITOCHONDRIAL ENCEPHALOMYOPATHY

被引:108
作者
OZAWA, T
TANAKA, M
SUGIYAMA, S
INO, H
OHNO, K
HATTORI, K
OHBAYASHI, T
ITO, T
DEGUCHI, H
KAWAMURA, K
NAKANE, Y
HASHIBA, K
机构
[1] NAGOYA UNIV,FAC MED,DEPT INTERNAL MED,NAGOYA,AICHI 466,JAPAN
[2] OSAKA MED COLL,DEPT INTERNAL MED,TAKATSUKI,OSAKA 569,JAPAN
[3] NAGASAKI UNIV,SCH MED,DEPT INTERNAL MED,NAGASAKI 852,JAPAN
关键词
D O I
10.1016/0006-291X(91)92014-B
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
Comparison of total mitochondrial DNA sequences of patients with idiopathic (delated or hypertrophic) cardiomyopathy with those of patients with Parkinson's disease and mitochondrial encephalomyopathies revealed distinct clustering of point mutations among patients. Furthermore, an inverse relation was found between the total number of base-substitution and life span of the patients. Among point mutations found in each patient, sequentially diverged six clusters consisting of 14, 10, 7, 1, 2, and 3 mutations, respectively, were detected. Five sub-clusters consisting of 2, 2, 11, 1, and 1 mutations, respectively, were detected. From each cluster, the patient's unique mutations were diverged with three types of the mutations specific for the disease. The divergence allowed construction of a phylogenetic tree which clearly indicated that patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathies. © 1991.
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收藏
页码:518 / 525
页数:8
相关论文
共 15 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]  
BRISTOW MR, 1980, BIOMEDICAL CLIN ASPE, P179
[3]   STRUCTURAL CONSERVATION AND VARIATION IN THE D-LOOP-CONTAINING REGION OF VERTEBRATE MITOCHONDRIAL-DNA [J].
BROWN, GG ;
GADALETA, G ;
PEPE, G ;
SACCONE, C ;
SBISA, E .
JOURNAL OF MOLECULAR BIOLOGY, 1986, 192 (03) :503-511
[4]  
HATTORI K, 1990, IN PRESS AM J CARDIO
[5]  
HAYAKAWA M, 1991, IN PRESS BIOCH BIOPH
[6]   INCREASE OF DELETED MITOCHONDRIAL-DNA IN THE STRIATUM IN PARKINSONS-DISEASE AND SENESCENCE [J].
IKEBE, S ;
TANAKA, M ;
OHNO, K ;
SATO, W ;
HATTORI, K ;
KONDO, T ;
MIZUNO, Y ;
OZAWA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :1044-1048
[7]   MITOCHONDRIAL LEUCINE TRANSFER-RNA MUTATION IN A MITOCHONDRIAL ENCEPHALOMYOPATHY [J].
INO, H ;
TANAKA, M ;
OHNO, K ;
HATTORI, K ;
IKEBE, S ;
SANO, T ;
OZAWA, T ;
ICHIKI, T ;
KOBAYASHI, M ;
WADA, Y .
LANCET, 1991, 337 (8735) :234-235
[8]   MITOCHONDRIAL-DNA MUTATIONS AS AN IMPORTANT CONTRIBUTOR TO AGEING AND DEGENERATIVE DISEASES [J].
LINNANE, AW ;
OZAWA, T ;
MARZUKI, S ;
TANAKA, M .
LANCET, 1989, 1 (8639) :642-645
[9]   MULTIPLE MITOCHONDRIAL-DNA DELETIONS EXIST IN CARDIOMYOCYTES OF PATIENTS WITH HYPERTROPHIC OR DILATED CARDIOMYOPATHY [J].
OZAWA, T ;
TANAKA, M ;
SUGIYAMA, S ;
HATTORI, K ;
ITO, T ;
OHNO, K ;
TAKAHASHI, A ;
SATO, W ;
TAKADA, G ;
MAYUMI, B ;
YAMAMOTO, K ;
ADACHI, K ;
KOGA, Y ;
TOSHIMA, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (02) :830-836
[10]   DISTINCT CLUSTERING OF POINT MUTATIONS IN MITOCHONDRIAL-DNA AMONG PATIENTS WITH MITOCHONDRIAL ENCEPHALOMYOPATHIES AND WITH PARKINSONS-DISEASE [J].
OZAWA, T ;
TANAKA, M ;
INO, H ;
OHNO, K ;
SANO, T ;
WADA, Y ;
YONEDA, M ;
TANNO, Y ;
MIYATAKE, T ;
TANAKA, T ;
ITOYAMA, S ;
IKEBE, S ;
HATTORI, N ;
MIZUNO, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 176 (02) :938-946