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- W118396048 abstract "Treatment of cells with DNA-damaging agents like UV irradiation or alkylating chemicals is known to greatly stimulate mono- and poly(ADPR) formation [1, 2] and turnover [3, 4]. Although there are many attempts to elucidate the function of poly(ADP-ribosyl)ation in DNA repair, the role of cellular mono(ADP-ribosyl)ation in the course of DNA damage has received relatively little attention. Recently Kreimeyer et al. [5] were able to demonstrate that histones were extensively mono(ADP-ribosyl)ated in intact DMS-treated hepatoma AH7974 cells. 20–30% of DMS-induced mono(ADPR) was found to be associated with histone H1 and nearly 60% with core histones. Adamietz et al. [6] identified histone H2B as the main acceptor of mono(ADPR) under these conditions. Surprisingly, mono(ADPR)-Hl as well as mono(ADPR)-H2B conjugates seemed to be resistant towards neutral hydroxylamine, indicating a linkage between ADPR and histone that was different from the ester glycosidic bond observed with poly(ADPR) in liver nuclei [5]." @default.
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- W118396048 date "1985-01-01" @default.
- W118396048 modified "2023-09-27" @default.
- W118396048 title "Mono(ADP-Ribosyl) Histone H1 in Alkylated Hepatoma Cells: Unusual Acceptor Site" @default.
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- W118396048 doi "https://doi.org/10.1007/978-3-642-70589-2_35" @default.
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