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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
18
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pubmed:dateCreated |
1998-9-28
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pubmed:abstractText |
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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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-1327967,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-1480111,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-1544898,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-1730246,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-1740190,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-1974461,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-2938257,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-2948950,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-3526158,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-6214787,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-6235522,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-6749845,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7019728,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7710119,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7747518,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7845219,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7876097,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7957078,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-7988699,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8146662,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8226758,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8248235,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8276800,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8354406,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8387896,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8592446,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-8810243,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-9149530,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-9390551,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-9405361,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9724747-9534168
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
95
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
10584-9
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:9724747-ATP-Dependent Proteases,
pubmed-meshheading:9724747-Adenosine Triphosphatases,
pubmed-meshheading:9724747-Amino Acid Sequence,
pubmed-meshheading:9724747-Base Sequence,
pubmed-meshheading:9724747-Biopolymers,
pubmed-meshheading:9724747-DNA Primers,
pubmed-meshheading:9724747-Heat-Shock Proteins,
pubmed-meshheading:9724747-Hydrolysis,
pubmed-meshheading:9724747-Mitochondria,
pubmed-meshheading:9724747-Oxygen,
pubmed-meshheading:9724747-Protein Binding,
pubmed-meshheading:9724747-Saccharomyces cerevisiae,
pubmed-meshheading:9724747-Serine Endopeptidases
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pubmed:year |
1998
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pubmed:articleTitle |
The ATPase and protease domains of yeast mitochondrial Lon: roles in proteolysis and respiration-dependent growth.
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pubmed:affiliation |
Department of Pharmaceutical Biology, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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