Plant mitochondria contain at least two i-AAA-like complexes

被引:74
作者
Urantowka, A
Knorpp, C
Olczak, T
Kolodziejczak, M
Janska, H
机构
[1] Univ Wroclaw, Inst Biochem & Mol Biol, Mol Cell Biol Lab, PL-51148 Wroclaw, Poland
[2] Dept Plant Biol & Forest Genet, S-75007 Uppsala, Sweden
关键词
Arabidopsis thaliana; ATP-dependent proteases; FtsH; i-AAA proteases; plant mitochondria;
D O I
10.1007/s11103-005-8766-3
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 FtsH proteases, also called AAA proteases, are membrane-bound ATP-dependent metalloproteases. The Arabidopsis genome contains a total of 12 FtsH-like genes. Two of them, AtFtsH4 and AtFtsH11, encode proteins with a high similarity to Yme1p, a subunit of the i-AAA complex in yeast mitochondria. Phylogenetic analysis groups the AtFtsH4, AtFtsH11 and Yme1 proteins together, with AtFtsH4 being the most similar to Yme1. Using immunological method we demonstrate here that AtFtsH4 is an exclusively mitochondrial protein while AtFtsH11 is found in both chloroplasts and mitochondria. AtFtsH4 and AtFtsH11 proteases are integral parts of the inner mitochondrial membrane and expose their catalytic sites towards the intermembrane space, same as yeast i-AAA. Database searches revealed that orthologs of AtFtsH4 and AtFtsH11 are present in both monocotyledonous and dicotyledonous plants. The two plant i-AAA proteases differ significantly in their termini: the FtsH4 proteins have a characteristic alanine stretch at the C-terminal end while FtsH11s have long N-terminal extensions. Blue-native gel electrophoresis revealed that AtFtsH4 and AtFtsH11 form at least two complexes with apparent molecular masses of about 1500 kDa. This finding implies that plants, in contrast to fungi and metazoa, have more than one complex with a topology similar to that of yeast i-AAA.
引用
收藏
页码:239 / 252
页数:14
相关论文
共 45 条
[11]  
DAVIS LG, 1994, BASIC METHODS MOL BI, P497
[12]   New insights into the respiratory chain of plant mitochondria.: Supercomplexes and a unique composition of complex II [J].
Eubel, H ;
Jänsch, L ;
Braun, HP .
PLANT PHYSIOLOGY, 2003, 133 (01) :274-286
[13]  
Gari E, 1997, YEAST, V13, P837, DOI 10.1002/(SICI)1097-0061(199707)13:9<837::AID-YEA145>3.0.CO
[14]  
2-T
[15]   VARIANT MITOCHONDRIAL PROTEIN AND DNA PATTERNS ASSOCIATED WITH CYTOPLASMIC MALE-STERILE LINES OF NICOTIANA [J].
HAKANSSON, G ;
VANDERMARK, F ;
BONNETT, HT ;
GLIMELIUS, K .
THEORETICAL AND APPLIED GENETICS, 1988, 76 (03) :431-437
[16]  
Hamel P, 1998, GENETICS, V150, P601
[17]   Experimental analysis of the Arabidopsis mitochondrial proteome highlights signaling and regulatory components, provides assessment of targeting prediction programs, and indicates plant-specific mitochondrial proteins [J].
Heazlewood, JL ;
Tonti-Filippini, JS ;
Gout, AM ;
Day, DA ;
Whelan, J ;
Millar, AH .
PLANT CELL, 2004, 16 (01) :241-256
[18]   Proteomic approach to characterize the supramolecular organization of photosystems in higher plants [J].
Heinemeyer, J ;
Eubel, H ;
Wehmhöner, D ;
Jänsch, L ;
Braun, HP .
PHYTOCHEMISTRY, 2004, 65 (12) :1683-1692
[19]   MAP-1 and IAP-1, two novel AAA proteases with catalytic sites on opposite membrane surfaces in mitochondrial inner membrane of Neurospora crassa [J].
Klanner, C ;
Prokisch, H ;
Langer, T .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (09) :2858-2869
[20]   A higher plant mitochondrial homologue of the yeast m-AAA protease - Molecular cloning, localization, and putative function [J].
Kolodziejczak, M ;
Kolaczkowska, A ;
Szczesny, B ;
Urantowka, A ;
Knorpp, C ;
Kieleczawa, J ;
Janska, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) :43792-43798