{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T02:44:43Z","timestamp":1791081883121,"version":"4.1.0"},"reference-count":58,"publisher":"The Company of Biologists","issue":"10","license":[{"start":{"date-parts":[[1997,5,15]],"date-time":"1997-05-15T00:00:00Z","timestamp":863654400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/www.biologists.com\/user-licence-1-1\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1997,5,15]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n               <jats:p>A UV-damaged DNA binding protein (UV-DDB) is the major source of UV-damaged DNA binding activity in mammalian cell extracts. This activity is defective in at least some xeroderma pigmentosum group E (XP-E) patients; microinjection of the UV-DDB protein into their fibroblasts corrects nucleotide excision repair (NER). In an in vitro reconstituted NER system, small amounts of UV-DDB stimulate repair synthesis a few fold. After exposure to UV, mammalian cells show an early dose-dependent inhibition of the extractable UV-DDB activity; this inhibition may reflect a tight association of the binding protein with UV-damaged genomic DNA. To investigate the dynamics and location of UV-DDB with respect to damaged chromatin in vivo, we utilized nuclear fractionation and specific antibodies and detected translocation of the p127 component of UV-DDB from a loose to a tight association with chromatinized DNA immediately after UV treatment.<\/jats:p>\n               <jats:p>A similar redistribution was found for other NER proteins, i.e. XPA, RP-A and PCNA, suggesting their tighter association with genomic DNA after UV. These studies revealed a specific protein-protein interaction between UV-DDB\/p127 and RP-A that appears to enhance binding of both proteins to UV-damaged DNA in vitro, providing evidence for the involvement of UV-DDB in the damage-recognition step of NER. Moreover, the kinetics of the reappearance of extractable UV-DDB activity after UV treatment of human cells with differing repair capacities positively correlate with the cell\u2019s capacity to repair 6-4 pyrimidine dimers (6-4 PD) in the whole genome, a result consistent with an in vivo role for UV-DDB in recognizing this type of UV lesion.<\/jats:p>","DOI":"10.1242\/jcs.110.10.1159","type":"journal-article","created":{"date-parts":[[2021,4,25]],"date-time":"2021-04-25T16:46:04Z","timestamp":1619369164000},"page":"1159-1168","source":"Crossref","is-referenced-by-count":61,"title":["Translocation of a UV-damaged DNA binding protein into a tight association with chromatin after treatment of mammalian cells with UV light"],"prefix":"10.1242","volume":"110","author":[{"given":"Vesna","family":"Rapi\u0107 Otrin","sequence":"first","affiliation":[{"name":"Section on DNA Replication, Repair and Mutagenesis, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mary","family":"McLenigan","sequence":"additional","affiliation":[{"name":"Section on DNA Replication, Repair and Mutagenesis, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masashi","family":"Takao","sequence":"additional","affiliation":[{"name":"Section on DNA Replication, Repair and Mutagenesis, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arthur S.","family":"Levine","sequence":"additional","affiliation":[{"name":"Section on DNA Replication, Repair and Mutagenesis, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Miroslava","family":"Proti\u0107","sequence":"additional","affiliation":[{"name":"Section on DNA Replication, Repair and Mutagenesis, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[1997,5,15]]},"reference":[{"key":"2024010400151034400_JOCES_110_10_1159C1","doi-asserted-by":"publisher","first-page":"859","DOI":"10.1016\/0092-8674(95)90289-9","article-title":"Mammalian DNA nucleotide excision repair reconstituted with purified protein components","volume":"80","author":"Aboussekhra","year":"1995","journal-title":"Cell"},{"key":"2024010400151034400_JOCES_110_10_1159C2","doi-asserted-by":"publisher","first-page":"326","DOI":"10.1006\/excr.1995.1382","article-title":"Detection of excision repair incisions in human fibroblast by immunostaining for PCNA","volume":"221","author":"Aboussekhra","year":"1995","journal-title":"Exp. 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