Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1991-5-21
pubmed:abstractText
Yeast cells containing the recessive mas3 mutation display temperature-sensitive defects in both mitochondrial protein import and the cell division cycle. The import defect is characterized by two pools of mitochondrial precursors and a dramatically slower rate of posttranslational import. The effect of mas3 on cell cycle progression occurs within one cell cycle at the nonpermissive temperature and retards progression through the G2 stage. The mas3 mutation maps to the gene encoding yeast heat-shock transcription factor (HSF), and expression of wild-type HSF complements the temperature-sensitive defects. The mas3 lesion has no apparent effect on protein secretion. In mas3 cells, induction of a major heat-shock gene, SSA1, is defective at 37 degrees C. The properties of the mas3 mutant cells indicate that HSF mediates the response to stress of two basic cellular processes: mitochondrial protein import and cell cycle progression.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2190988, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2197269, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2234077, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2250717, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2427013, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2556404, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2563898, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2645524, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2651414, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2659436, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2674677, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2687285, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-2853609, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3004964, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3044612, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3044613, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3044780, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3058716, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3061808, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3282178, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3282179, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3306402, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3327750, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3510081, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-3542970, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-375221, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6215406, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6232136, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6235522, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6290489, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6290491, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6315400, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6336730, http://linkedlifedata.com/resource/pubmed/commentcorrection/2017170-6754086
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0270-7306
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:geneSymbol
mas3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2647-55
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1991
pubmed:articleTitle
A mutation in the yeast heat-shock factor gene causes temperature-sensitive defects in both mitochondrial protein import and the cell cycle.
pubmed:affiliation
Department of Biology, University of California, San Diego, La Jolla 92093.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't