Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
1994-11-18
pubmed:abstractText
The RAD6 gene of Saccharomyces cerevisiae encodes a ubiquitin-conjugating enzyme that is required for postreplication repair of UV-damaged DNA, DNA damage induced mutagenesis, sporulation, and amino-end rule protein degradation. RAD6 interacts physically with the UBR1 gene product in carrying out the multiubiquitination of amino-end rule proteolytic substrates. In mediating postreplication repair, it has remained unclear whether RAD6 acts in a pleiotropic manner distal from the site of DNA damage or is targeted to the damage site via interaction with another repair component. Here, we show that RAD6 forms a specific complex with the product of the DNA repair gene RAD18. The biological significance of this interaction is attested by the observation that overproduction of the rad6 Ala-88 mutant protein, which lacks ubiquitin-conjugating activity but retains the ability to interact with RAD18 protein, confers a high level of UV sensitivity on wild-type RAD+ cells that can be corrected by the concomitant overexpression of RAD18. We demonstrate that whereas RAD6 has no affinity for DNA, RAD18 binds single-stranded DNA. Thus, association of RAD6 with RAD18 could provide a means for targeting RAD6 to damage-containing DNA regions, where the RAD6 ubiquitin-conjugating function could modulate the activity of a stalled DNA replication machinery. We also show that RAD6 forms separate complexes with RAD18 and with UBR1, and the extremely conserved amino terminus of RAD6 that is required for complex formation with UBR1 is dispensable for complex formation with RAD18.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Fungal, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Fungal, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Single-Stranded, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Ligases, http://linkedlifedata.com/resource/pubmed/chemical/RAD18 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/RAD6 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/UBR1 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Conjugating Enzymes, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligases
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0890-9369
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
8
pubmed:geneSymbol
RAD18, RAD6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
811-20
pubmed:dateRevised
2009-6-17
pubmed:meshHeading
pubmed-meshheading:7926769-Antibodies, Fungal, pubmed-meshheading:7926769-Conserved Sequence, pubmed-meshheading:7926769-DNA, Fungal, pubmed-meshheading:7926769-DNA, Single-Stranded, pubmed-meshheading:7926769-DNA Damage, pubmed-meshheading:7926769-DNA Repair, pubmed-meshheading:7926769-DNA-Binding Proteins, pubmed-meshheading:7926769-Fungal Proteins, pubmed-meshheading:7926769-Gene Expression, pubmed-meshheading:7926769-Genes, Fungal, pubmed-meshheading:7926769-Humans, pubmed-meshheading:7926769-Ligases, pubmed-meshheading:7926769-Models, Biological, pubmed-meshheading:7926769-Mutation, pubmed-meshheading:7926769-Protein Binding, pubmed-meshheading:7926769-Saccharomyces cerevisiae, pubmed-meshheading:7926769-Saccharomyces cerevisiae Proteins, pubmed-meshheading:7926769-Ubiquitin-Conjugating Enzymes, pubmed-meshheading:7926769-Ubiquitin-Protein Ligases
pubmed:year
1994
pubmed:articleTitle
Specific complex formation between yeast RAD6 and RAD18 proteins: a potential mechanism for targeting RAD6 ubiquitin-conjugating activity to DNA damage sites.
pubmed:affiliation
Department of Biophysics, University of Rochester, New York 14642.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.