Essential role of Mia40 in import and assembly of mitochondrial intermembrane space proteins

被引:345
作者
Chacinska, A
Pfannschmidt, S
Wiedemann, N
Kozjak, V
Szklarz, LKS
Schulze-Specking, A
Truscott, KN
Guiard, B
Meisinger, C
Pfanner, N
机构
[1] Univ Freiburg, Inst Biochem & Molekularbiol, D-79104 Freiburg, Germany
[2] Univ Freiburg, Fak Biol, D-79104 Freiburg, Germany
[3] Univ Paris 06, Ctr Genet Mol, Lab Propre CNRS Assoc, Gif Sur Yvette, France
关键词
mitochondrial intermembrane space; protein assembly; protein sorting; Saccharomyces cerevisiae; Tim proteins;
D O I
10.1038/sj.emboj.7600389
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
Mitochondria import nuclear-encoded precursor proteins to four different subcompartments. Specific import machineries have been identified that direct the precursor proteins to the mitochondrial outer membrane, inner membrane or matrix, respectively. However, a machinery dedicated to the import of mitochondrial intermembrane space (IMS) proteins has not been found so far. We have identified the essential IMS protein Mia40 (encoded by the Saccharomyces cerevisiae open reading frame YKL195w). Mitochondria with a mutant form of Mia40 are selectively inhibited in the import of several small IMS proteins, including the essential proteins Tim9 and Tim10. The import of proteins to the other mitochondrial subcompartments does not depend on functional Mia40. The binding of small Tim proteins to Mia40 is crucial for their transport across the outer membrane and represents an initial step in their assembly into IMS complexes. We conclude that Mia40 is a central component of the protein import and assembly machinery of the mitochondrial IMS.
引用
收藏
页码:3735 / 3746
页数:12
相关论文
共 54 条
  • [1] Tim9, a new component of the TIM22•54 translocase in mitochondria
    Adam, A
    Endres, M
    Sirrenberg, C
    Lottspeich, F
    Neupert, W
    Brunner, M
    [J]. EMBO JOURNAL, 1999, 18 (02) : 313 - 319
  • [2] Juxtaposition of the two distal CX3C motifs via intrachain disulfide bonding is essential for the folding of Tim10
    Allen, S
    Lu, H
    Thornton, D
    Tokatlidis, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (40) : 38505 - 38513
  • [3] Purification, characterization, and localization of yeast Cox17p, a mitochondrial copper shuttle
    Beers, J
    Glerum, DM
    Tzagoloff, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (52) : 33191 - 33196
  • [4] The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins
    Curran, SP
    Leuenberger, D
    Schmidt, E
    Koehler, CM
    [J]. JOURNAL OF CELL BIOLOGY, 2002, 158 (06) : 1017 - 1027
  • [5] The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier
    Curran, SP
    Leuenberger, D
    Oppliger, W
    Koehler, CM
    [J]. EMBO JOURNAL, 2002, 21 (05) : 942 - 953
  • [6] Two intermembrane space TIM complexes interact with different domains of Tim23p during its import into mitochondria
    Davis, AJ
    Sepuri, NB
    Holder, J
    Johnson, AE
    Jensen, RE
    [J]. JOURNAL OF CELL BIOLOGY, 2000, 150 (06) : 1271 - 1282
  • [7] The Tim core complex defines the number of mitochondrial translocation contact sites and can hold arrested preproteins in the absence of matrix Hsp70-Tim44
    Dekker, PJT
    Martin, F
    Maarse, AC
    Bomer, U
    Muller, H
    Guiard, B
    Meijer, M
    Rassow, J
    Pfanner, N
    [J]. EMBO JOURNAL, 1997, 16 (17) : 5408 - 5419
  • [8] Dekker PJT, 1996, BIOL CHEM, V377, P535
  • [9] Apocytochrome c requires the TOM complex for translocation across the mitochondrial outer membrane
    Diekert, K
    de Kroon, AIPM
    Ahting, U
    Niggemeyer, B
    Neupert, W
    de Kruijff, B
    Lill, R
    [J]. EMBO JOURNAL, 2001, 20 (20) : 5626 - 5635
  • [10] ROLE OF CYTOCHROME-C HEME LYASE IN MITOCHONDRIAL IMPORT AND ACCUMULATION OF CYTOCHROME-C IN SACCHAROMYCES-CEREVISIAE
    DUMONT, ME
    CARDILLO, TS
    HAYES, MK
    SHERMAN, F
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (11) : 5487 - 5496