Literature DB >> 9724747

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

J M van Dijl1, E Kutejová, K Suda, D Perecko, G Schatz, C K Suzuki.   

Abstract

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.

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Year:  1998        PMID: 9724747      PMCID: PMC27938          DOI: 10.1073/pnas.95.18.10584

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  31 in total

Review 1.  The mechanism and functions of ATP-dependent proteases in bacterial and animal cells.

Authors:  A L Goldberg
Journal:  Eur J Biochem       Date:  1992-01-15

2.  Structural analysis of GroE chaperonin complexes using chemical cross-linking.

Authors:  A Azem; C Weiss; P Goloubinoff
Journal:  Methods Enzymol       Date:  1998       Impact factor: 1.600

3.  Cell biology. An unfolding story of protein translocation.

Authors:  J E Rothman; R D Kornberg
Journal:  Nature       Date:  1986 Jul 17-23       Impact factor: 49.962

4.  Two nuclear mutations that block mitochondrial protein import in yeast.

Authors:  M P Yaffe; G Schatz
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

5.  Protease La from Escherichia coli hydrolyzes ATP and proteins in a linked fashion.

Authors:  L Waxman; A L Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

6.  E. coli contains eight soluble proteolytic activities, one being ATP dependent.

Authors:  K H Swamy; A L Goldberg
Journal:  Nature       Date:  1981-08-13       Impact factor: 49.962

7.  Selectivity of intracellular proteolysis: protein substrates activate the ATP-dependent protease (La).

Authors:  L Waxman; A L Goldberg
Journal:  Science       Date:  1986-04-25       Impact factor: 47.728

8.  Chaperonin-facilitated refolding of ribulosebisphosphate carboxylase and ATP hydrolysis by chaperonin 60 (groEL) are K+ dependent.

Authors:  P V Viitanen; T H Lubben; J Reed; P Goloubinoff; D P O'Keefe; G H Lorimer
Journal:  Biochemistry       Date:  1990-06-19       Impact factor: 3.162

Review 9.  Proteases and protein degradation in Escherichia coli.

Authors:  M R Maurizi
Journal:  Experientia       Date:  1992-02-15

10.  The energy utilized in protein breakdown by the ATP-dependent protease (La) from Escherichia coli.

Authors:  A S Menon; L Waxman; A L Goldberg
Journal:  J Biol Chem       Date:  1987-01-15       Impact factor: 5.157

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  25 in total

1.  Turnover of matrix proteins in mammalian mitochondria.

Authors:  Walter Huth; Stefan Rolle; Ilona Wunderlich
Journal:  Biochem J       Date:  2002-05-15       Impact factor: 3.857

2.  The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier.

Authors:  Sean P Curran; Danielle Leuenberger; Wolfgang Oppliger; Carla M Koehler
Journal:  EMBO J       Date:  2002-03-01       Impact factor: 11.598

3.  Mitochondrial Lon of Saccharomyces cerevisiae is a ring-shaped protease with seven flexible subunits.

Authors:  H Stahlberg; E Kutejová; K Suda; B Wolpensinger; A Lustig; G Schatz; A Engel; C K Suzuki
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

Review 4.  Slicing a protease: structural features of the ATP-dependent Lon proteases gleaned from investigations of isolated domains.

Authors:  Tatyana V Rotanova; Istvan Botos; Edward E Melnikov; Fatima Rasulova; Alla Gustchina; Michael R Maurizi; Alexander Wlodawer
Journal:  Protein Sci       Date:  2006-08       Impact factor: 6.725

5.  Single-turnover kinetic experiments confirm the existence of high- and low-affinity ATPase sites in Escherichia coli Lon protease.

Authors:  Diana Vineyard; Jessica Patterson-Ward; Irene Lee
Journal:  Biochemistry       Date:  2006-04-11       Impact factor: 3.162

Review 6.  Degradation of excess peroxisomes in mammalian liver cells by autophagy and other mechanisms.

Authors:  Sadaki Yokota; H Dariush Fahimi
Journal:  Histochem Cell Biol       Date:  2009-02-20       Impact factor: 4.304

7.  ATP-dependent proteases differ substantially in their ability to unfold globular proteins.

Authors:  Prakash Koodathingal; Neil E Jaffe; Daniel A Kraut; Sumit Prakash; Susan Fishbain; Christophe Herman; Andreas Matouschek
Journal:  J Biol Chem       Date:  2009-04-21       Impact factor: 5.157

8.  Induction of peroxisomal Lon protease in rat liver after di-(2-ethylhexyl)phthalate treatment.

Authors:  Sadaki Yokota; Celina M Haraguchi; Toshiaki Oda
Journal:  Histochem Cell Biol       Date:  2007-10-11       Impact factor: 4.304

9.  A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.

Authors:  A Seyda; R F Newbold; T J Hudson; A Verner; N MacKay; S Winter; A Feigenbaum; S Malaney; D Gonzalez-Halphen; A P Cuthbert; B H Robinson
Journal:  Am J Hum Genet       Date:  2001-01-10       Impact factor: 11.025

10.  Evidence that two ATP-dependent (Lon) proteases in Borrelia burgdorferi serve different functions.

Authors:  James L Coleman; Laura I Katona; Christopher Kuhlow; Alvaro Toledo; Nihal A Okan; Rafal Tokarz; Jorge L Benach
Journal:  PLoS Pathog       Date:  2009-11-26       Impact factor: 6.823

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