Vizirianakis I S, Tsiftsoglou A S
Department of Pharmaceutical Sciences, Aristotle University of Thessaloniki, Greece.
Biochim Biophys Acta. 1996 Jun 5;1312(1):8-20. doi: 10.1016/0167-4889(96)00012-2.
Murine erythroleukemia (MEL) cells exposed to DMSO were assessed for their ability to methylate poly(A)+ RNA and accumulate RNA transcripts of globin and nonglobin genes (c-myc, beta-actin and MER5). Cells were pulse-labeled with L-[methyl-3H]methionine, cytoplasmic RNA was isolated, selected for poly(A)+ RNA and analyzed by HPLC chromatography for methylated nucleosides. When MEL cells were exposed to inhibitors of RNA methylation (neplanocin A, 3-deazaneplanocin A and cycloleucine) and assessed for their ability to differentiate by DMSO, accumulate RNA transcripts, produce hemoglobin, methylate poly(A)+ and poly(A)- RNA and synthesize S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH), we observed the following: (a) MEL cells treated with DMSO underwent hypermethylation in poly(A)+ RNA that preferentially occurred at the 5'-cap structures (7-methylguanosine and 2'-O-methylcytidine and 2'-O-methyluridine); (b) inducer-treated MEL cells exhibited a decrease in the intracellular level of SAH that led to a lower ratio of SAH/SAM, an event that favors methylation; and (c) treatment of MEL cells with inhibitors of RNA methylation suppressed methylation of poly(A)- and poly(A)+ RNA, reversed the ratio SAH/SAM seen in differentiated MEL cells and prevented differentiation to occur. Moreover, we observed that treatment of MEL cells with selective inhibitors of RNA methylation caused fragmentation of beta major globin and c-myc mRNAs, two RNA transcripts coded by developmentally regulated genes, while had no detectable effect on the structural integrity of poly(A)+ RNA transcripts transcribed by two housekeeping genes (beta-actin and MER5). These data indicate that induction of erythroid cell differentiation of MEL cells is associated with changes in methylation of poly(A)+ RNA and selective differential stability of RNA transcripts, two events that might be related to each other.
对暴露于二甲基亚砜(DMSO)的小鼠红白血病(MEL)细胞进行评估,检测其对多聚腺苷酸(poly(A)+)RNA甲基化以及积累珠蛋白和非珠蛋白基因(c-myc、β-肌动蛋白和MER5)RNA转录本的能力。用L-[甲基-³H]甲硫氨酸对细胞进行脉冲标记,分离细胞质RNA,选择多聚腺苷酸(poly(A)+)RNA并通过高效液相色谱法分析甲基化核苷。当MEL细胞暴露于RNA甲基化抑制剂(奈替米星A、3-去氮奈替米星A和环亮氨酸),并评估其被DMSO诱导分化、积累RNA转录本、产生血红蛋白、对多聚腺苷酸(poly(A)+)和多聚腺苷酸(poly(A)-)RNA甲基化以及合成S-腺苷甲硫氨酸(SAM)和S-腺苷同型半胱氨酸(SAH)的能力时,我们观察到以下情况:(a)用DMSO处理的MEL细胞在多聚腺苷酸(poly(A)+)RNA中发生了超甲基化,这种超甲基化优先发生在5'-帽结构(7-甲基鸟苷、2'-O-甲基胞苷和2'-O-甲基尿苷);(b)经诱导剂处理的MEL细胞细胞内SAH水平降低,导致SAH/SAM比值降低,这有利于甲基化;(c)用RNA甲基化抑制剂处理MEL细胞可抑制多聚腺苷酸(poly(A)-)和多聚腺苷酸(poly(A)+)RNA的甲基化,逆转分化的MEL细胞中观察到的SAH/SAM比值,并阻止分化发生。此外,我们观察到用RNA甲基化选择性抑制剂处理MEL细胞会导致β-珠蛋白和c-myc mRNA片段化,这两种RNA转录本由发育调控基因编码,而对两个管家基因(β-肌动蛋白和MER5)转录的多聚腺苷酸(poly(A)+)RNA转录本的结构完整性没有可检测到的影响。这些数据表明,MEL细胞红系细胞分化的诱导与多聚腺苷酸(poly(A)+)RNA甲基化的变化以及RNA转录本的选择性差异稳定性有关,这两个事件可能相互关联。