DIFFERENTIAL EXPRESSION OF GENES SPECIFYING 2 ISOFORMS OF SUBUNIT-VIA OF HUMAN CYTOCHROME-C-OXIDASE

被引:36
作者
FABRIZI, GM
SADLOCK, J
HIRANO, M
MITA, S
KOGA, Y
RIZZUTO, R
ZEVIANI, M
SCHON, EA
机构
[1] COLUMBIA UNIV COLL PHYS & SURG, DEPT NEUROL, 630 W 168TH ST, NEW YORK, NY 10032 USA
[2] COLUMBIA UNIV COLL PHYS & SURG, NEW YORK, NY 10032 USA
[3] IST NEUROCHIRURG C BESTA, MILAN, ITALY
[4] COLUMBIA UNIV COLL PHYS & SURG, DEPT GENET & DEV, NEW YORK, NY 10032 USA
关键词
MITOCHONDRIAL PROTEIN; NUCLEAR GENE; RESPIRATORY CHAIN; ELECTRON TRANSPORT; RECOMBINANT DNA; NUCLEOTIDE SEQUENCE ANALYSIS; MUSCLE; LIVER;
D O I
10.1016/0378-1119(92)90288-Z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Subunit VIa of mammalian cytochrome c oxidase (COX; EC 1.9.3.1.) exists in two isoforms, one present ubiquitously ('liver' isoform; COX VIa-L) and the other present only in cardiac and skeletal muscle (COX VIa-M). We have now isolated a full-length cDNA specifying human COX VIa-M. The deduced mature COX VIa-M polypeptide is 62% identical to the human COX VIa-L isoform, but is approximately 80% identical to the bovine and rat COX VIa-M isoforms, suggesting that the two COX VIa isoform-encoding genes arose prior to the mammalian radiation. Transcriptional analysis showed a tissue-specific pattern: whereas COXVIa-L is transcribed ubiquitously, COXVIa-M is transcribed only in heart and skeletal muscle. The cDNA specifying COX VIa-M is a prime candidate for use in investigations of Mendelian-inherited COX deficiences with primary involvement of muscle.
引用
收藏
页码:307 / 312
页数:6
相关论文
共 37 条
[1]   TISSUE-SPECIFIC EXPRESSION AND CHROMOSOME ASSIGNMENT OF GENES SPECIFYING 2 ISOFORMS OF SUBUNIT-VIIA OF HUMAN CYTOCHROME-C-OXIDASE [J].
ARNAUDO, E ;
HIRANO, M ;
SEELAN, RS ;
MILATOVICH, A ;
HSIEH, CL ;
FABRIZI, GM ;
GROSSMAN, LI ;
FRANCKE, U ;
SCHON, EA .
GENE, 1992, 119 (02) :299-305
[2]   FATAL INFANTILE CYTOCHROME-C OXIDASE DEFICIENCY - DECREASE OF IMMUNOLOGICALLY DETECTABLE ENZYME IN MUSCLE [J].
BRESOLIN, N ;
ZEVIANI, M ;
BONILLA, E ;
MILLER, RH ;
LEECH, RW ;
SHANSKE, S ;
NAKAGAWA, M ;
DIMAURO, S .
NEUROLOGY, 1985, 35 (06) :802-812
[3]   INFLUENCE OF BUFFER COMPOSITION, MEMBRANE-LIPIDS AND PROTEASES ON THE KINETICS OF RECONSTITUTED CYTOCHROME-C-OXIDASE FROM BOVINE LIVER AND HEART [J].
BUGE, U ;
KADENBACH, B .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 161 (02) :383-390
[4]  
CAO X, 1988, ANN NY ACAD SCI, V550, P337, DOI 10.1111/j.1749-6632.1988.tb35348.x
[5]   COMPLEXITY AND TISSUE-SPECIFICITY OF THE MITOCHONDRIAL RESPIRATORY-CHAIN [J].
CAPALDI, RA ;
HALPHEN, DG ;
ZHANG, YZ ;
YANAMURA, W .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1988, 20 (03) :291-311
[6]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[7]   MOLECULAR DEFECTS IN CYTOCHROME-OXIDASE IN MITOCHONDRIAL DISEASES [J].
DIMAURO, S ;
ZEVIANI, M ;
RIZZUTO, R ;
LOMBES, A ;
NAKASE, H ;
BONILLA, E ;
MIRANDA, A ;
SCHON, E .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1988, 20 (03) :353-364
[8]   MITOCHONDRIAL MYOPATHIES [J].
DIMAURO, S ;
BONILLA, E ;
ZEVIANI, M ;
NAKAGAWA, M ;
DEVIVO, DC .
ANNALS OF NEUROLOGY, 1985, 17 (06) :521-538
[9]   SWITCHING OF BOVINE CYTOCHROME-C-OXIDASE SUBUNIT VIA ISOFORMS IN SKELETAL-MUSCLE DURING DEVELOPMENT [J].
EWART, GD ;
ZHANG, YZ ;
CAPALDI, RA .
FEBS LETTERS, 1991, 292 (1-2) :79-84
[10]   SEQUENCE OF A CDNA SPECIFYING SUBUNIT-VIA OF HUMAN CYTOCHROME-C OXIDASE [J].
FABRIZI, GM ;
RIZZUTO, R ;
NAKASE, H ;
MITA, S ;
KADENBACH, B ;
SCHON, EA .
NUCLEIC ACIDS RESEARCH, 1989, 17 (15) :6409-6409