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2-氨基苯甲酰胺是一种ADP-核糖基化抑制剂,它可拮抗N'-甲基烟酰胺诱导的小鼠Friend红白血病细胞分化过程中的DNA低甲基化。

2-Aminobenzamide, an inhibitor of ADP-ribosylation, antagonizes induced DNA hypomethylation during differentiation of murine Friend erythroleukemia cells by N'-methylnicotinamide.

作者信息

Kuykendall J R, Cox R

机构信息

Cancer Research Laboratory, Veterans Administration Medical Center, Memphis, TN 38104.

出版信息

Differentiation. 1990 Jul;44(1):69-73. doi: 10.1111/j.1432-0436.1990.tb00538.x.

Abstract

The ADP-ribose synthesis inhibitor 2-aminobenzamide was found to reduce the induction of haemoglobin synthesis in murine Friend erythroleukemia cells, cultured continuously for 96 h with 5 mM N'-methylnicotinamide, with over 50% inhibition at equimolar doses. 2-Aminobenzamide was optimally effective as an inhibitor of differentiation if present only during the time period 24-48 h after initial N'-methylnicotinamide exposure. A transient, genome-wide DNA hypomethylation accompanies induction by N'-methylnicotinamide. Although 2-aminobenzamide does not seem to affect normal DNA methylation in cultured cells, the observed DNA hypomethylation in cells cultured for 24 h with 5 mM N'-methylnicotinamide was antagonized over 50% by equimolar 2-aminobenzamide. We suggest that ADP-ribosylation has a positive modulatory role in erythroid differentiation, and possibly in the process(es) leading to DNA hypomethylation following inducer exposure.

摘要

ADP-核糖合成抑制剂2-氨基苯甲酰胺被发现可降低小鼠Friend红白血病细胞中血红蛋白合成的诱导,该细胞用5 mM N'-甲基烟酰胺连续培养96小时,在等摩尔剂量下抑制率超过50%。如果仅在最初暴露于N'-甲基烟酰胺后的24-48小时内存在,2-氨基苯甲酰胺作为分化抑制剂的效果最佳。N'-甲基烟酰胺诱导伴随着短暂的全基因组DNA低甲基化。虽然2-氨基苯甲酰胺似乎不影响培养细胞中的正常DNA甲基化,但在5 mM N'-甲基烟酰胺培养24小时的细胞中观察到的DNA低甲基化被等摩尔的2-氨基苯甲酰胺拮抗超过50%。我们认为ADP-核糖基化在红系分化中具有正向调节作用,并且可能在诱导剂暴露后导致DNA低甲基化的过程中起作用。

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