XPC branch‐point sequence mutations disrupt U2 snRNP binding,resulting in abnormal pre‐mRNA splicing in xeroderma pigmentosum patients |
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Authors: | Sikandar G Khan Koji Yamanegi Zhi‐Ming Zheng Jennifer Boyle Kyoko Imoto Kyu‐Seon Oh Carl C Baker Engin Gozukara Ahmet Metin Kenneth H Kraemer |
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Institution: | 1. Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland;2. HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland;3. Laboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland;4. Department of Biochemistry, Inonu University Medical School, Malatya, Turkey;5. Department of Dermatology, Yuzuncu Yil University Medical School, Van, Turkey |
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Abstract: | Mutations in two branch‐point sequences (BPS) in intron 3 of the XPC DNA repair gene affect pre‐mRNA splicing in association with xeroderma pigmentosum (XP) with many skin cancers (XP101TMA) or no skin cancer (XP72TMA), respectively. To investigate the mechanism of these abnormalities we now report that transfection of minigenes with these mutations revealed abnormal XPC pre‐mRNA splicing that mimicked pre‐mRNA splicing in the patients' cells. DNA oligonucleotide‐directed RNase H digestion demonstrated that mutations in these BPS disrupt U2 snRNP–BPS interaction. XP101TMA cells had no detectable XPC protein but XP72TMA had 29% of normal levels. A small amount of XPC protein was detected at sites of localized ultraviolet (UV)‐damaged DNA in XP72TMA cells which then recruited other nucleotide excision repair (NER) proteins. In contrast, XP101TMA cells had no detectable recruitment of XPC or other NER proteins. Post‐UV survival and photoproduct assays revealed greater reduction in DNA repair in XP101TMA cells than in XP72TMA. Thus mutations in XPC BPS resulted in disruption of U2 snRNP‐BPS interaction leading to abnormal pre‐mRNA splicing and reduced XPC protein. At the cellular level these changes were associated with features of reduced DNA repair including diminished NER protein recruitment, reduced post‐UV survival and impaired photoproduct removal. Hum Mutat 30:1–9, 2009. Published 2009 Wiley‐Liss, Inc. |
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Keywords: | XPC DNA repair pre‐mRNA splicing xeroderma pigmentosum skin cancer U2 snRNP |
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