Natural competence of mammalian mitochondria allows the molecular investigation of mitochondrial gene expression

被引:72
作者
Koulintchenko, M
Temperley, RJ
Mason, PA
Dietrich, A
Lightowlers, RN [1 ]
机构
[1] Univ Newcastle Upon Tyne, Inst Neurosci, Mitochondrial Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Univ Newcastle Upon Tyne, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[3] Univ Strasbourg 1, CNRS, Inst Biol Mol Plantes, F-67084 Strasbourg, France
[4] RAS, Siberian Inst Plant Physiol & Biochem, Irkutsk 664033, Russia
基金
英国惠康基金;
关键词
D O I
10.1093/hmg/ddi435
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
Respiration, a fundamental process in mammalian cells, requires two genomes, those of the nucleus and the mitochondrion (mtDNA). Mutations of mtDNA are being increasingly recognized in disease and may play an important role in the ageing process. Accepting the vital role of mtDNA gene products, our limited knowledge concerning the details of mitochondrial gene expression is surprising. This is, in part, due to our inability to transfect mitochondria and to manipulate their genome. There have been claims of successful DNA import into isolated organelles, but most reports lacked evidence of expression and no method has furthered our understanding of gene expression. Here, we report that mammalian mitochondria possess a natural competence for DNA import. Using five functional assays, we show imported DNA can act as templates for DNA synthesis or promoter-driven transcription, with the resultant polycistronic RNA being processed (5' and 3') and excised mt-tRNA matured. Exploiting this natural competence will allow us to explore mitochondrial gene expression in organello and provides the potential for mitochondrial transfection in vivo.
引用
收藏
页码:143 / 154
页数:12
相关论文
共 46 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]   The genome sequence of Rickettsia prowazekii and the origin of mitochondria [J].
Andersson, SGE ;
Zomorodipour, A ;
Andersson, JO ;
Sicheritz-Pontén, T ;
Alsmark, UCM ;
Podowski, RM ;
Näslund, AK ;
Eriksson, AS ;
Winkler, HH ;
Kurland, CG .
NATURE, 1998, 396 (6707) :133-140
[3]   REGULATION OF MITOCHONDRIAL GENE-EXPRESSION IN MAMMALIAN-CELLS [J].
ATTARDI, G ;
CHOMYN, A ;
KING, MP ;
KRUSE, B ;
POLOSA, PL ;
MURDTER, NN .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (04) :509-513
[4]  
BEATTIE DS, 1967, J BIOL CHEM, V242, P3366
[5]   IDENTIFICATION OF A PROMOTER FOR TRANSCRIPTION OF THE HEAVY STRAND OF HUMAN MTDNA - INVITRO TRANSCRIPTION AND DELETION MUTAGENESIS [J].
BOGENHAGEN, DF ;
APPLEGATE, EF ;
YOZA, BK .
CELL, 1984, 36 (04) :1105-1113
[6]  
BRANDON MC, 2005, MITOMAP HUMAN MITOCH
[7]   IDENTIFICATION BY IN ORGANELLO FOOTPRINTING OF PROTEIN CONTACT SITES AND OF SINGLE-STRANDED-DNA SEQUENCES IN THE REGULATORY REGION OF RAT MITOCHONDRIAL-DNA - PROTEIN-BINDING SITES AND SINGLE-STRANDED-DNA REGIONS IN ISOLATED RAT-LIVER MITOCHONDRIA [J].
CANTATORE, P ;
DADDABBO, L ;
FRACASSO, F ;
GADALETA, MN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :25020-25027
[8]   PRECISE IDENTIFICATION OF INDIVIDUAL PROMOTERS FOR TRANSCRIPTION OF EACH STRAND OF HUMAN MITOCHONDRIAL-DNA [J].
CHANG, DD ;
CLAYTON, DA .
CELL, 1984, 36 (03) :635-643
[9]   DNA uptake during bacterial transformation [J].
Chen, I ;
Dubnau, D .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (03) :241-249
[10]   A TRIDECAMER DNA-SEQUENCE SUPPORTS HUMAN MITOCHONDRIAL RNA 3'-END FORMATION INVITRO [J].
CHRISTIANSON, TW ;
CLAYTON, DA .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (10) :4502-4509