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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2001-4-16
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pubmed:abstractText |
The yeast two-hybrid system was used to screen for proteins that interact in vivo with Saccharomyces cerevisiae Rpg1p/Tif32p, the large subunit of the translation initiation factor 3 core complex (eIF3). Eight positive clones encoding portions of the SLA2/END4/MOP2 gene were isolated. They overlapped in the region of amino acids 318-550. Subsequent deletion analysis of Sla2p showed that amino acids 318-373 were essential for the two-hybrid protein-protein interaction. The N-terminal part of Rpg1p (aa 1-615) was essential and sufficient for the Rpg1p-Sla2p interaction. A coimmunoprecipitation assay provided additional evidence for the physical interaction of Rpg1p/Tif32p with Sla2p in vivo. Using immunofluorescence microscopy, Rpg1p and Sla2p proteins were colocalized at the patch associated with the tip of emerging bud. Considering the essential role of Rpg1p as the large subunit of the eIF3 core complex and the association of Sla2p with the actin cytoskeleton, a putative role of the Rpg1p-Sla2p interaction in localized translation is discussed.
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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 |
http://linkedlifedata.com/resource/pubmed/chemical/Actins,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Eukaryotic Initiation Factor-3,
http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Initiation Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Subunits,
http://linkedlifedata.com/resource/pubmed/chemical/RPG1 protein, S cerevisiae,
http://linkedlifedata.com/resource/pubmed/chemical/SLA2 protein, S cerevisiae,
http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0006-291X
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2001 Academic Press.
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pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
282
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1244-50
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11302750-Actins,
pubmed-meshheading:11302750-Carrier Proteins,
pubmed-meshheading:11302750-Cell Cycle Proteins,
pubmed-meshheading:11302750-Cytoskeletal Proteins,
pubmed-meshheading:11302750-Cytoskeleton,
pubmed-meshheading:11302750-Eukaryotic Initiation Factor-3,
pubmed-meshheading:11302750-Fluorescent Antibody Technique,
pubmed-meshheading:11302750-Fungal Proteins,
pubmed-meshheading:11302750-Genes, Reporter,
pubmed-meshheading:11302750-Mutagenesis, Site-Directed,
pubmed-meshheading:11302750-Peptide Initiation Factors,
pubmed-meshheading:11302750-Precipitin Tests,
pubmed-meshheading:11302750-Protein Binding,
pubmed-meshheading:11302750-Protein Structure, Tertiary,
pubmed-meshheading:11302750-Protein Subunits,
pubmed-meshheading:11302750-Saccharomyces cerevisiae,
pubmed-meshheading:11302750-Saccharomyces cerevisiae Proteins,
pubmed-meshheading:11302750-Two-Hybrid System Techniques
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pubmed:year |
2001
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pubmed:articleTitle |
Rpg1p/Tif32p, a subunit of translation initiation factor 3, interacts with actin-associated protein Sla2p.
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pubmed:affiliation |
Vienna Biocenter, Institute of Biochemistry and Molecular Cell Biology, University of Vienna, Austria.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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