The ATPase and protease domains of yeast mitochondrial Lon:: Roles in proteolysis and respiration-dependent growth

被引:59
作者
van Dijl, JM
Kutejová, E
Suda, K
Perecko, D
Schatz, G
Suzuki, CK
机构
[1] Biozentrum, CH-4056 Basel, Switzerland
[2] Univ Groningen, Dept Pharmaceut Biol, NL-9713 AV Groningen, Netherlands
[3] Slovak Acad Sci, Inst Mol Biol, Bratislava 84251, Slovakia
关键词
D O I
10.1073/pnas.95.18.10584
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ATP-dependent Lon protease of Saccharomyces cerevisiae mitochondria is required for selective proteolysis in the matrix, maintenance of mitochondrial DNA, and respiration-dependent growth. Lon may also possess a chaperone-like function that facilitates protein degradation and protein-complex assembly. To understand the influence of Lon's ATPase and protease activities on these functions, we examined several Lon mutants for their ability to complement defects of Lon-deleted yeast cells, We also developed a rapid procedure for purifying yeast Lon to homogeneity to study the enzyme's activities and oligomeric state. A point mutation in either the ATPase or the protease site strongly inhibited the corresponding activity of the pure protein but did not alter the protein's oligomerization; when expressed at normal low levels neither of these mutant enzymes supported respiration-dependent growth of Lon-deleted cells. When the ATPase- or the protease-containing regions of Lon were expressed as separate truncated proteins, neither could support respiration-dependent growth of Lon-deleted cells; however, coexpression of these two separated regions sustained wild-type growth. These results suggest that yeast Lon contains two catalytic domains that can interact with one another even as separate proteins, and that both are essential for the different functions of Lon.
引用
收藏
页码:10584 / 10589
页数:6
相关论文
共 34 条
[21]  
Sambrook J., 2002, MOL CLONING LAB MANU
[22]   ATP-dependent proteases that also chaperone protein biogenesis [J].
Suzuki, CK ;
Rep, M ;
vanDijl, JM ;
Suda, K ;
Grivell, LA ;
Schatz, G .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (04) :118-123
[23]   REQUIREMENT FOR THE YEAST GENE LON IN INTRAMITOCHONDRIAL PROTEOLYSIS AND MAINTENANCE OF RESPIRATION [J].
SUZUKI, CK ;
SUDA, K ;
WANG, N ;
SCHATZ, G .
SCIENCE, 1994, 264 (5156) :273-276
[24]   ESCHERICHIA-COLI CONTAINS 8 SOLUBLE PROTEOLYTIC ACTIVITIES, ONE BEING ATP DEPENDENT [J].
SWAMY, KHS ;
GOLDBERG, AL .
NATURE, 1981, 292 (5824) :652-654
[25]   IDENTIFICATION OF THE POTENTIAL ACTIVE-SITE OF THE SIGNAL PEPTIDASE SIPS OF BACILLUS-SUBTILIS - STRUCTURAL AND FUNCTIONAL SIMILARITIES WITH LEXA-LIKE PROTEASES [J].
VANDIJL, JM ;
DEJONG, A ;
VENEMA, G ;
BRON, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :3611-3618
[26]  
VANDYCK L, 1994, J BIOL CHEM, V269, P238
[27]   CHAPERONIN-FACILITATED REFOLDING OF RIBULOSEBISPHOSPHATE CARBOXYLASE AND ATP HYDROLYSIS BY CHAPERONIN-60 (GROEL) ARE K+ DEPENDENT [J].
VIITANEN, PV ;
LUBBEN, TH ;
REED, J ;
GOLOUBINOFF, P ;
OKEEFE, DP ;
LORIMER, GH .
BIOCHEMISTRY, 1990, 29 (24) :5665-5671
[28]   NEW HETEROLOGOUS MODULES FOR CLASSICAL OR PCR-BASED GENE DISRUPTIONS IN SACCHAROMYCES-CEREVISIAE [J].
WACH, A ;
BRACHAT, A ;
POHLMANN, R ;
PHILIPPSEN, P .
YEAST, 1994, 10 (13) :1793-1808
[29]   MOLECULAR CHAPERONES COOPERATE WITH PIM1 PROTEASE IN THE DEGRADATION OF MISFOLDED PROTEINS IN MITOCHONDRIA [J].
WAGNER, I ;
ARLT, H ;
VANDYCK, L ;
LANGER, T ;
NEUPERT, W .
EMBO JOURNAL, 1994, 13 (21) :5135-5145
[30]  
WAGNER J, 1997, EMBO J, V16, P7317