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Both cross-links and monoadducts induced in DNA by psoralens can lead to sister chromatid exchange formation

Journal Article · · Experimental Cell Research; (United States)
 [1]; ; ; ;  [2]
  1. Univ. of California, San Francisco (United States) Facultad de Biologia, Sevilla (Spain)
  2. Univ. of California, San Francisco (United States)
The relative importance of DNA-DNA cross-links and bulky monoadducts in sister chromatid exchange (SCE) formation was investigated in three human fibroblast cell lines with different repair capabilities. These cell lines included normal cells, which can repair both classes of lesion; xeroderma pigmentosum (XP) cells, which cannot repair either psoralen-induced cross-links or monoadducts; and an XP revertant that repairs only cross-links and not monoadducts. SCEs were induced by two psoralen derivatives. After activation with long-wave ultraviolet light, HMT produces cross-links and monoadducts in DNA, whereas 5-MIP produces only monoadducts. In normal human cells both psoralens induced SCEs, but if cells were allowed to repair for 18 h before bromodeoxyuridine (BrdUrd) was added for SCE analysis, the SCE frequency was significantly reduced. XP cells showed an SCE frequency that remained high regardless of whether SCEs were analyzed immediately after psoralen exposure of 18 h later. In the XP revertant that repairs only cross-links, both psoralens induced a high yield of SCEs when BrdUrd was added immediately after psoralen treatment. These observations indicate that both cross-links and monoadducts are lesions in DNA that can lead to SCE formation.
DOE Contract Number:
AC03-76SF01012
OSTI ID:
5376827
Journal Information:
Experimental Cell Research; (United States), Journal Name: Experimental Cell Research; (United States) Vol. 196:1; ISSN ECREA; ISSN 0014-4827
Country of Publication:
United States
Language:
English

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