| pubmed-article:10601031 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10601031 | lifeskim:mentions | umls-concept:C0043393 | lld:lifeskim |
| pubmed-article:10601031 | lifeskim:mentions | umls-concept:C0524550 | lld:lifeskim |
| pubmed-article:10601031 | lifeskim:mentions | umls-concept:C1167622 | lld:lifeskim |
| pubmed-article:10601031 | lifeskim:mentions | umls-concept:C1521761 | lld:lifeskim |
| pubmed-article:10601031 | lifeskim:mentions | umls-concept:C0598313 | lld:lifeskim |
| pubmed-article:10601031 | lifeskim:mentions | umls-concept:C1314939 | lld:lifeskim |
| pubmed-article:10601031 | pubmed:issue | 23 | lld:pubmed |
| pubmed-article:10601031 | pubmed:dateCreated | 2000-1-11 | lld:pubmed |
| pubmed-article:10601031 | pubmed:abstractText | Nucleotide excision repair (NER) in yeast is effected by the concerted action of a large complex of proteins. Recently, we identified a stable subcomplex containing the yeast Rad7 and Rad16 proteins. Here, we report the identification of autonomously replicating sequence binding factor 1 (ABF1) as a component of the Rad7/Rad16 NER subcomplex. Yeast ABF1 protein is encoded by an essential gene required for DNA replication, transcriptional regulation, and gene silencing. We show that ABF1 plays a direct role in NER in vitro. Additionally, consistent with a role of ABF1 protein in NER in vivo, we show that certain temperature-sensitive abf1 mutant strains that are defective in DNA replication are specifically defective in the removal of photoproducts by NER and are sensitive to killing by ultraviolet (UV) radiation. These studies define a novel and unexpected role for ABF1 protein during NER in yeast. | lld:pubmed |
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| pubmed-article:10601031 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:10601031 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:10601031 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10601031 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:10601031 | pubmed:issn | 0890-9369 | lld:pubmed |
| pubmed-article:10601031 | pubmed:author | pubmed-author:AkiyamaMM | lld:pubmed |
| pubmed-article:10601031 | pubmed:author | pubmed-author:FriedbergE... | lld:pubmed |
| pubmed-article:10601031 | pubmed:author | pubmed-author:StillmanBB | lld:pubmed |
| pubmed-article:10601031 | pubmed:author | pubmed-author:ReedS HSH | lld:pubmed |
| pubmed-article:10601031 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10601031 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:10601031 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:10601031 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10601031 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10601031 | pubmed:pagination | 3052-8 | lld:pubmed |
| pubmed-article:10601031 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:10601031 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10601031 | pubmed:articleTitle | Yeast autonomously replicating sequence binding factor is involved in nucleotide excision repair. | lld:pubmed |
| pubmed-article:10601031 | pubmed:affiliation | Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA. | lld:pubmed |
| pubmed-article:10601031 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10601031 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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