Dual localization of human DNA topoisomerase IIIα to mitochondria and nucleus

被引:94
作者
Wang, Y [1 ]
Lyu, YL [1 ]
Wang, JC [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1073/pnas.192449499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human TOP3alpha gene encoding DNA topoisomerase Ilia (hTop3alpha) has two potential start codons for the synthesis of proteins 1,001 and 976 aa residues in length. The sequence of the N-terminal region of the 1,001-residue form resembles signal peptide sequences for mitochondrial import, and fluorescence microscopy shows that the addition of as few as the first 34 aa of the 1,001-residue form of hTop3alpha to a green fluorescent protein can direct the chimeric protein to mitochondria. Biochemical analyses of subcellular fractions of HeLa cells further demonstrate that a distinctive fraction of hTop3alpha is present inside mitochondria, as evidenced by its resistance to proteinase K. This fraction constitutes several percent of the enzyme in the nuclear fraction, suggesting that the distribution of the mitochondrial and nuclear forms of hTop3alpha is roughly in proportion to the DNA contents of these cellular compartments. The presence of a type IA DNA topoisomerase in the mitochondria of other eukaryotes is supported by an examination of the amino acid sequences of mouse and Drosophila DNA topoisomerase IIIalpha and Schizosaccharomyces pombe DNA topoisomerase III. Given the presence of at least one type IA DNA topoisomerase in all forms of life examined to date, the finding of a type IA enzyme in mitochondria further supports the notion of a key role of such enzymes in DNA transactions.
引用
收藏
页码:12114 / 12119
页数:6
相关论文
共 64 条
[1]  
Bennett RJ, 2000, J BIOL CHEM, V275, P26898
[2]   Association of yeast DNA topoisomerase III and Sgs1 DNA helicase: Studies of fusion proteins [J].
Bennett, RJ ;
Wang, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) :11108-11113
[3]   An atypical topoisomerase II from archaea with implications for meiotic recombination [J].
Bergerat, A ;
deMassy, B ;
Gadelle, D ;
Varoutas, PC ;
Nicolas, A ;
Forterre, P .
NATURE, 1997, 386 (6623) :414-417
[4]   DNA topoisomerases: Structure, function, and mechanism [J].
Champoux, JJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :369-413
[5]  
CHAVALITSHEWINK.P, 2001, ASIAN J TROP MED PUB, V32, P733
[6]   Computational method to predict mitochondrially imported proteins and their targeting sequences [J].
Claros, MG ;
Vincens, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 241 (03) :779-786
[7]   An alternate form of Ku80 is required for DNA end-binding activity in mammalian mitochondria [J].
Coffey, G ;
Campbell, C .
NUCLEIC ACIDS RESEARCH, 2000, 28 (19) :3793-3800
[8]   Mitochondrial DNA repair pathways [J].
Croteau, DL ;
Stierum, RH ;
Bohr, VA .
MUTATION RESEARCH-DNA REPAIR, 1999, 434 (03) :137-148
[9]   THE YEAST TYPE-I TOPOISOMERASE TOP3 INTERACTS WITH SGS1, A DNA HELICASE HOMOLOG - A POTENTIAL EUKARYOTIC REVERSE GYRASE [J].
GANGLOFF, S ;
MCDONALD, JP ;
BENDIXEN, C ;
ARTHUR, L ;
ROTHSTEIN, R .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8391-8398
[10]   CLEAVAGE-SITE MOTIFS IN MITOCHONDRIAL TARGETING PEPTIDES [J].
GAVEL, Y ;
VONHEIJNE, G .
PROTEIN ENGINEERING, 1990, 4 (01) :33-37