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http://bura.brunel.ac.uk/handle/2438/3898
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DC Field | Value | Language |
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dc.contributor.author | Abbaszadeh, F | - |
dc.contributor.author | Clingen, PH | - |
dc.contributor.author | Arlett, CF | - |
dc.contributor.author | Plowman, PN | - |
dc.contributor.author | Bourton, EC | - |
dc.contributor.author | Themis, M | - |
dc.contributor.author | Makarov, EM | - |
dc.contributor.author | Newbold, RF | - |
dc.contributor.author | Green, MHL | - |
dc.contributor.author | Parris, CN | - |
dc.date.accessioned | 2009-11-26T14:35:13Z | - |
dc.date.available | 2009-11-26T14:35:13Z | - |
dc.date.issued | 2009 | - |
dc.identifier.citation | Journal of Medical Genetics. 46(11): 1-24 | en |
dc.identifier.issn | 1468-6244 | - |
dc.identifier.uri | http://jmg.bmj.com/content/early/2009/10/01/jmg.2009.068866.abstract?sid=bbe12cac-a832-43a1-865d-1bb6d9716b7e | en |
dc.identifier.uri | http://bura.brunel.ac.uk/handle/2438/3898 | - |
dc.description | This article has been made available through the Brunel Open Access Publishing Fund. | - |
dc.description.abstract | Background: Radiotherapy-induced DNA double strand breaks (DSB) are critical cytotoxic lesions. Inherited defects in DSB DNA repair pathways lead to hypersensitivity to ionising radiation, immunodeficiency and increased cancer incidence. A patient with xeroderma pigmentosum complementation group C, with a scalp angiosarcoma exhibited dramatic clinical radiosensitivity following radiotherapy, resulting in death. A fibroblast cell line from non-affected skin (XP14BRneo17) was hypersensitive to ionising radiation and defective in DNA double strand break repair. Aim: To determine the genetic defect causing cellular radiation hypersensitivity in XP14BRneo17 cells. Methods: Functional genetic complementation whereby copies of human chromosomes containing genes involved in DNA DSB repair (chromosomes 2, 5, 8 10, 13 and 22) were individually transferred to XP14BRneo17 cells in an attempt to correct the radiation hypersensitivity. Clonogenic survival assays and γ-H2AX immunofluorescence were conducted to measure radiation sensitivity and repair of DNA DSBs. DNA sequencing of defective DNA repair genes was performed. Results: Transfer of chromosome 8 (location of DNA-PKcs gene), and transfection of a mammalian expression construct containing the DNA-PKcs cDNA restored normal ionising radiation sensitivity and repair of DNA DSBs in XP14BRneo17 cells. DNA sequencing of the DNA-PKcs coding region revealed a 249 bp deletion (between base pairs 3656-3904) encompassing exon 31 of the gene. Conclusion: We provide evidence of a novel splice variant of the DNA-PKcs gene associated with radiosensitivity in a xeroderma pigmentosum patient and report the first double mutant in distinct DNA repair pathways being consistent with viability. | en |
dc.description.sponsorship | Brunel Open Access Publishing Fund | en |
dc.language.iso | en | en |
dc.publisher | MBJ | en |
dc.subject | Functional complementation | en |
dc.subject | Radiosensitivity | en |
dc.subject | DNA repair | en |
dc.subject | DNA-PKcs gene | en |
dc.subject | Pre-mRNA | en |
dc.title | A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitvity in a xeroderma pigmentosum patient | en |
dc.type | Article | en |
Appears in Collections: | Biological Sciences Community Health and Public Health Brunel OA Publishing Fund Dept of Life Sciences Research Papers |
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Fulltext.pdf | 11.39 MB | Adobe PDF | View/Open |
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