Peroxisome Proliferator-activated Receptor γ Co-activator 1α (PGC-1α) and Sirtuin 1 (SIRT1) Reside in Mitochondria POSSIBLE DIRECT FUNCTION IN MITOCHONDRIAL BIOGENESIS

被引:277
作者
Aquilano, Katia [1 ]
Vigilanza, Paola [1 ]
Baldelli, Sara [1 ]
Pagliei, Beatrice [1 ]
Rotilio, Giuseppe [1 ,2 ]
Ciriolo, Maria Rosa [1 ,2 ]
机构
[1] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
[2] Ist Ricovero & Cura Carattere Sci, I-00165 Rome, Italy
关键词
TRANSCRIPTION-FACTOR-A; DNA; LOCALIZATION; ASSOCIATION; NUCLEOIDS; ENZYMES; MUSCLE; PGC-1; MTDNA;
D O I
10.1074/jbc.M109.070169
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
The transcriptional co-activator PGC-1 alpha and the NAD(+)-dependent deacetylase SIRT1 are considered important inducers of mitochondrial biogenesis because in the nucleus they regulate transcription of nucleus-encoded mitochondrial genes. We demonstrate that PGC-1 alpha and SIRT1 are also present inside mitochondria and are in close proximity to mtDNA. They interact with mitochondrial transcription factor A (TFAM) as assessed by confocal microscopy analysis and by blue native-PAGE. Nucleoid purification allowed us to identify SIRT1 and PGC-1 alpha as proteins associated with native and cross-linked nucleoids, respectively. After mtDNA immunoprecipitation analysis, carried out on mitochondrial extracts, we found that PGC-1 alpha is present on the same D-loop region recognized by TFAM. Finally, by oligonucleotide pulldown assay, we found PGC-1 alpha and SIRT1 associated with the TFAM consensus sequence (human mitochondrial transcription factor-binding site H). The results obtained suggest that in mitochondria PGC-1 alpha and SIRT1 may function as their nuclear counterparts and represent the genuine factors mediating the cross-talk between nuclear and mitochondrial genome. Finally, this work adds new knowledge on the function of SIRT1 and PGC-1 alpha and highlights the direct involvement of such proteins in regulation of mitochondrial biogenesis.
引用
收藏
页码:21590 / 21599
页数:10
相关论文
共 34 条
  • [21] Mitochondrial nucleoids undergo remodeling in response to metabolic cues
    Kucej, Martin
    Kucejova, Blanka
    Subramanian, Ramiah
    Chen, Xin Jie
    Butow, Ronald A.
    [J]. JOURNAL OF CELL SCIENCE, 2008, 121 (11) : 1861 - 1868
  • [22] Minireview: The PGC-1 Coactivator Networks: Chromatin-Remodeling and Mitochondrial Energy Metabolism
    Lin, Jiandie D.
    [J]. MOLECULAR ENDOCRINOLOGY, 2009, 23 (01) : 2 - 10
  • [23] LOWRY OH, 1951, J BIOL CHEM, V193, P265
  • [24] SIRT1 functionally interacts with the metabolic regulator and transcriptional coactivator PGC-1α
    Nemoto, S
    Fergusson, MM
    Finkel, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (16) : 16456 - 16460
  • [25] Mitochondrial glycerol-3-P acyltransferase 1 is most active in outer mitochondrial membrane but not in mitochondrial associated vesicles (MAV)
    Pellon-Malson, Magali
    Montanaro, Mauro A.
    Coleman, Rosalind A.
    Gonzalez-Baro, Maria R.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2007, 1771 (07): : 830 - 838
  • [26] A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis
    Puigserver, P
    Wu, ZD
    Park, CW
    Graves, R
    Wright, M
    Spiegelman, BM
    [J]. CELL, 1998, 92 (06) : 829 - 839
  • [27] Metabolic adaptations through the PGC-1α and SIRT1 pathways
    Rodgers, Joseph T.
    Lerin, Carles
    Gerhart-Hines, Zachary
    Puigserver, Pere
    [J]. FEBS LETTERS, 2008, 582 (01) : 46 - 53
  • [28] Transcriptional paradigms in mammalian mitochondrial biogenesis and function
    Scarpulla, Richard C.
    [J]. PHYSIOLOGICAL REVIEWS, 2008, 88 (02) : 611 - 638
  • [29] Substrates and regulation mechanisms for the human mitochondrial Sirtuins Sirt3 and Sirt5
    Schlicker, Christine
    Gertz, Melanie
    Papatheodorou, Panagiotis
    Kachholz, Barbara
    Becker, Christian F. W.
    Steegborn, Clemens
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2008, 382 (03) : 790 - 801
  • [30] Localization of GRP78 to mitochondria under the unfolded protein response
    Sun, Fang-Chun
    Wei, Shou
    Li, Chia-Wei
    Chang, Yuo-Sheng
    Chao, Chih-Chung
    Lai, Yiu-Kay
    [J]. BIOCHEMICAL JOURNAL, 2006, 396 : 31 - 39