Copper-dependence of mitochondrial DNA rearrangements in Podospora anserina

被引:27
作者
Borghouts, C [1 ]
Kerschner, S [1 ]
Osiewacz, HD [1 ]
机构
[1] Univ Frankfurt, Inst Bot, D-60439 Frankfurt, Germany
关键词
Podospora anserina; recombination; mitochondrial DNA; intron transposition;
D O I
10.1007/s002940050528
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rearrangements of the mitochondrial DNA (mtDNA) are a hallmark of senescence in wild-type strains of the ascomycete P, anserina. These rearrangements include the systematic amplification of the first intron (pl-intron) of the cytochrome oxidase subunit-I gene (CoI) as a circular DNA molecule (p1DNA). In addition. deletions and amplifications of other regions of the mtDNA occur. The molecular basis of the underlying processes is not understood in detail. A comparative analysis of the wild-type strain and of the long-lived mutant grisea, affected in the uptake of copper, revealed that mtDNA instabilities are dependent on the availability of cellular copper. In the mutant, the first steps in the corresponding pathway, including the transcription of the Col gene, the splicing of the pl-intron and the transposition of this mobile element, are not impaired. In contrast. recombination processes between short direct repeats, as well as rearrangements between two tandem intron copies leading to the formation of p1DNA, appear to be affected. Additional copper in the growth medium rescues this molecular phenotype. We suggest that copper is a cofactor of a component of the molecular machinery leading to the characteristic age-related mtDNA rearrangements.
引用
收藏
页码:268 / 275
页数:8
相关论文
共 54 条
[1]  
Barrientos A, 1996, AM J HUM GENET, V58, P963
[2]   MOBILE GROUP-II INTRONS, DNA CIRCLES, REVERSE-TRANSCRIPTASE AND SENESCENCE - (GROUP-II INTRONS, TRANSPOSITION, AGING, MITOCHONDRIA, FUNGI) [J].
BELCOUR, L ;
SAINSARDCHANET, A ;
SELLEM, CH .
GENETICA, 1994, 93 (1-3) :225-228
[3]   A SITE-SPECIFIC DELETION IN MITOCHONDRIAL-DNA OF PODOSPORA IS UNDER THE CONTROL OF NUCLEAR GENES [J].
BELCOUR, L ;
BEGEL, O ;
PICARD, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3579-3583
[4]   Singlet oxygen mediates the UVA-induced generation of the photoaging-associated mitochondrial common deletion [J].
Berneburg, M ;
Grether-Beck, S ;
Kürten, V ;
Ruzicka, T ;
Briviba, K ;
Sies, H ;
Krutmann, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (22) :15345-15349
[5]   HYPERACTIVE RECOMBINATION IN THE MITOCHONDRIAL-DNA OF THE NATURAL DEATH NUCLEAR MUTANT OF NEUROSPORA-CRASSA [J].
BERTRAND, H ;
WU, QM ;
SEIDELROGOL, BL .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (11) :6778-6788
[6]  
BLOK RB, 1995, HUM GENET, V95, P75
[7]   Mitochondrial DNA rearrangements of Podospora anserina are under the control of the nuclear gene grisea [J].
Borghouts, C ;
Kimpel, E ;
Osiewacz, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10768-10773
[8]   GRISEA, a copper-modulated transcription factor from Podospora anserina involved in senescence and morphogenesis, is an ortholog of MAC1 in Saccharomyces cerevisiae [J].
Borghouts, C ;
Osiewacz, HD .
MOLECULAR AND GENERAL GENETICS, 1998, 260 (05) :492-502
[9]   EVIDENCE FOR CO-REGULATION OF CU,ZN SUPEROXIDE-DISMUTASE AND METALLOTHIONEIN GENE-EXPRESSION IN YEAST THROUGH TRANSCRIPTIONAL CONTROL BY COPPER VIA THE ACE 1-FACTOR [J].
CARRI, MT ;
GALIAZZO, F ;
CIRIOLO, MR ;
ROTILIO, G .
FEBS LETTERS, 1991, 278 (02) :263-266
[10]   MITOCHONDRIAL-DNA DELETIONS IN HUMAN BRAIN - REGIONAL VARIABILITY AND INCREASE WITH ADVANCED AGE [J].
CORRALDEBRINSKI, M ;
HORTON, T ;
LOTT, MT ;
SHOFFNER, JM ;
BEAL, MF ;
WALLACE, DC .
NATURE GENETICS, 1992, 2 (04) :324-329