The presequence of fumarase is exposed to the cytosol during import into mitochondria

被引:26
作者
Karniely, S [1 ]
Regev-Rudzki, N [1 ]
Pines, O [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Dept Biol Mol, IL-91120 Jerusalem, Israel
基金
以色列科学基金会;
关键词
fumarase; co-translational translocation; mitochondrial import; dual distribution; presequence;
D O I
10.1016/j.jmb.2006.02.023
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 majority of mitochondrial proteins can be imported into mitochondria following termination of their translation in the cytosol. Import of fumarase and several other proteins into mitochondria does not appear to occur post-translationally according to standard in vivo and in vitro assays. However, the nature of interaction between the translation and translocation apparatuses during import of these proteins is unknown. Therefore, a major question is whether the nascent chains of these proteins are exposed to the cytosol during import into mitochondria. We asked directly if the presequence of fumarase can be cleaved by externally added mitochondrial processing peptidase (MPP) during import, using an in vitro translation-translocation coupled reaction. The presequence of fumarase was cleaved by externally added MPP during import, indicating a lack of, or a loose physical connection between, the translation and translocation of this protein. Exchanging the authentic presequence of fumarase for that of the more efficient Su9-ATPase presequence reduced the exposure of fumarase precursors to externally added MPP en route to mitochondria. Therefore, exposure to cytosolic MPP is dependent on the presequence and not on the mature part of fumarase. On the other hand, following translation in the absence of mitochondria, the authentic fumarase presequence and that of Su9-ATPase become inaccessible to added MPP when attached to mature fumarase. Thus, folding of the mature portion of fumarase, which conceals the presequence, is the reason for its inability to be imported in classical post-translational assays. Another unique feature of fumarase is its distribution between the mitochondria and the cytosol. We show that in vivo the switch of the authentic presequence with that of Su9-ATPase caused more fumarase molecules to be localized to the mitochondria. A possible mechanism by which the cytosolic exposure, the targeting efficiency, and the subcellular distribution of fumarase are dictated by the presequence is discussed. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:396 / 405
页数:10
相关论文
共 29 条
[1]  
ADES IZ, 1980, J BIOL CHEM, V255, P9925
[2]  
ADES IZ, 1980, J BIOL CHEM, V255, P9918
[3]   Two parameters improve efficiency of mitochondrial uptake of adenylate kinase:: decreased folding velocity and increased propensity of N-terminal α-helix formation [J].
Angermayr, M ;
Strobel, G ;
Zollner, A ;
Korber, D ;
Bandlow, W .
FEBS LETTERS, 2001, 508 (03) :427-432
[4]   YEAST ADENYLATE KINASE IS ACTIVE SIMULTANEOUSLY IN MITOCHONDRIA AND CYTOPLASM AND IS REQUIRED FOR NON-FERMENTATIVE GROWTH [J].
BANDLOW, W ;
STROBEL, G ;
ZOGLOWEK, C ;
OECHSNER, U ;
MAGDOLEN, V .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 178 (02) :451-457
[5]  
Becker J, 1996, MOL CELL BIOL, V16, P4378
[6]  
BLACHINSKI E, 2001, THESIS HEBEW U
[7]   In yeast, the 3′ untranslated region or the presequence of ATM1 is required for the exclusive localization of its mRNA to the vicinity of mitochondria [J].
Corral-Debrinski, M ;
Blugeon, C ;
Jacq, C .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (21) :7881-7892
[8]  
DAUM G, 1982, J BIOL CHEM, V257, P3028
[9]   CYTOPLASMIC TYPE-80S RIBOSOMES ASSOCIATED WITH YEAST MITOCHONDRIA .4. ATTACHMENT OF RIBOSOMES TO OUTER MEMBRANE OF ISOLATED-MITOCHONDRIA [J].
KELLEMS, RE ;
ALLISON, VF ;
BUTOW, RA .
JOURNAL OF CELL BIOLOGY, 1975, 65 (01) :1-14
[10]   Import into mitochondria, folding and retrograde movement of fumarase in yeast [J].
Knox, C ;
Sass, E ;
Neupert, W ;
Pines, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :25587-25593