Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies

被引:14
作者
Arredondo, Juan J. [1 ]
Esther Gallardo, M. [1 ,2 ]
Garcia-Pavia, Pablo [3 ,4 ]
Domingo, Veronica [1 ]
Breton, Begona [1 ]
Teresa Garcia-Silva, M. [5 ]
Jesus Sedano, M. [6 ]
Martin, Miguel A. [2 ,7 ]
Arenas, Joaquin [2 ,7 ]
Cervera, Margarita [1 ]
Garesse, Rafael [1 ,2 ]
Bornstein, Belen [1 ,2 ,8 ]
机构
[1] Univ Autonoma Madrid, Fac Med, CSIC, Dept Bioquim,Inst Invest Biomed Alberto Sols, E-28029 Madrid, Spain
[2] CIBERER, Madrid, Spain
[3] Hosp Univ Puerta de Hierro, Serv Cardiol, Madrid, Spain
[4] Red Invest Clin & Basica Insuficiencia Cardiaca R, Madrid, Spain
[5] Hosp Univ 12 Octubre, Serv Pediat, Madrid, Spain
[6] Hosp Gen Yague, Serv Neurol, Burgos, Spain
[7] Hosp Univ 12 Octubre, Ctr Invest, Lab Enfermedades Mitocondriales, Madrid, Spain
[8] Hosp Univ Puerta de Hierro, Serv Bioquim, Madrid, Spain
关键词
Mitochondrial DNA; m.1628C > T; m.1644G > A; Mitochondrial tRNA quantification; Mitochondrial diseases; Mitochondrial cardiomyopathies; LACTIC-ACIDOSIS; DNA; GENE; TRNA(LYS); SEQUENCE; AMINOACYLATION; PATHOGENICITY; MYOPATHY; HISTORY;
D O I
10.1016/j.mito.2011.09.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of this study was to identify the genetic defect in two patients having cardiac dysfunction accompanied by neurological symptoms, and in one case MRI evidence of cortical and cerebellar atrophy with hyper-intensities in the basal ganglia. Muscle biopsies from each patient revealed single and combined mitochondrial respiratory chain deficiency. The complete mtDNA sequencing of both patients revealed two transitions in the mitochondrial tRNA(Val) gene (MT-TV) (m.1628C>T in Patient 1, and m.1644G>A in Patient 2). The functional and molecular analyses reported here suggest that the MT-TV gene should be routinely considered in the diagnosis of mitochondrial cardiomyopathies. (C) 2011 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
收藏
页码:357 / 362
页数:6
相关论文
共 46 条
[1]   OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes [J].
Amati-Bonneau, Patrizia ;
Valentino, Maria Lucia ;
Reynier, Pascal ;
Gallardo, Maria Esther ;
Bornstein, Belen ;
Boissiere, Anne ;
Campos, Yolanda ;
Rivera, Henry ;
de la Aleja, Jesus Gonzalez ;
Carroccia, Rosanna ;
Iommarini, Luisa ;
Labauge, Pierre ;
Figarella-Branger, Dominique ;
Marcorelles, Pascale ;
Furby, Alain ;
Beauvais, Katell ;
Letournel, Franck ;
Liguori, Rocco ;
La Morgia, Chiara ;
Montagna, Pasquale ;
Liguori, Maria ;
Zanna, Claudia ;
Rugolo, Michela ;
Cossarizza, Andrea ;
Wissinger, Bernd ;
Verny, Christophe ;
Schwarzenbacher, Robert ;
Martin, Miguel Angel ;
Arenas, Joaquin ;
Ayuso, Carmen ;
Garesse, Rafael ;
Lenaers, Guy ;
Bonneau, Dominique ;
Carelli, Valerio .
BRAIN, 2008, 131 :338-351
[2]   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
[3]   Quantification of mitochondrial DNA copy number: Pre-analytical factors [J].
Andreu, Antonio L. ;
Martinez, Ramiro ;
Marti, Ramon ;
Garcia-Arumi, Elena .
MITOCHONDRION, 2009, 9 (04) :242-246
[4]   Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA [J].
Andrews, RM ;
Kubacka, I ;
Chinnery, PF ;
Lightowlers, RN ;
Turnbull, DM ;
Howell, N .
NATURE GENETICS, 1999, 23 (02) :147-147
[5]   Decreased mitochondrial tRNALys steady-state levels and aminoacylation are associated with the pathogenic G8313A mitochondrial DNA mutation [J].
Bacman, SR ;
Atencio, DP ;
Moraes, CT .
BIOCHEMICAL JOURNAL, 2003, 374 :131-136
[6]   Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophlic cardiomyopathy and encephalopathy [J].
Bénit, P ;
Beugnot, R ;
Chretien, D ;
Giurgea, I ;
De Lonlay-Debeney, P ;
Issartel, JP ;
Corral-Debrinski, M ;
Kerscher, S ;
Rustin, P ;
Rötig, A ;
Munnich, A .
HUMAN MUTATION, 2003, 21 (06) :582-586
[7]   Childhood neurological presentation of a novel mitochondrial tRNAVal gene mutation [J].
Blakely, EL ;
Poulton, J ;
Pike, M ;
Wojnarowska, F ;
Turnbull, PM ;
McFarland, R ;
Taylor, RW .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 225 (1-2) :99-103
[8]   Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNALys gene [J].
Bornstein, B ;
Mas, JA ;
Patrono, C ;
Fernández-Moreno, MA ;
González-Vioque, E ;
Campos, Y ;
Carrozzo, R ;
Martín, MA ;
del Hoyo, P ;
Santorelli, FM ;
Arenas, J ;
Garesse, R .
BIOCHEMICAL JOURNAL, 2005, 387 :773-778
[9]   A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome [J].
Chalmers, RM ;
Lamont, PJ ;
Nelson, I ;
Ellison, DW ;
Thomas, NH ;
Harding, AE ;
Hammans, SR .
NEUROLOGY, 1997, 49 (02) :589-592
[10]   A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency [J].
Da Pozzo, Paola ;
Cardaioli, Elena ;
Malfatti, Edoardo ;
Gallus, Gian Nicola ;
Malandrini, Alessandro ;
Gaudiano, Carmen ;
Berti, Gianna ;
Invernizzi, Federica ;
Zeviani, Massimo ;
Federico, Antonio .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2009, 17 (08) :1092-1096