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Aflatoxin B-1 induced multiple epigenetic modulators in human epithelial cell lines

机译:黄曲霉毒素B-1在人上皮细胞系中诱导多个表观遗传调节剂

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摘要

The compulsive and insidious secondary metabolite aflatoxin B-1, produced by the opportunistic fungi Aspergillus flavus, upholds a distinguished place in midst of the toxicants causing fatal hazards to humans. Aflatoxins alter the function of host cells by inducing multiple effects through genetic and non-genetic pathways. Epigenetic mechanisms drag major attention towards finding novel and new mechanisms involved in this process. Our present work intends to study the functional expression profile of multiple epigenetic regulators. AFB i modulates multiple epigenetic regulators like DNA methyltransferases (DMNTs), histones modifying enzymes and polycomb proteins. AFB(1) upregulates the expression of DNMTs at gene and protein level in a dose dependent manner. It reduced the histone acetyl transferase (HAT) activity significantly with a remarkable increase in histone deacetylase (HDAC) activity along with an induction in expression of HDACs gene and protein in a dose dependent manner. The gene and protein expression of polycomb repressor proteins B cell specific moloney murine leukemia virus integration site 1 (BMI-1) and enhancer of zeste homolog 2 (EZH2) was significantly over expressed with enhanced trimethylation of H3K27 and ubiquitination of H2AK119. In summary, our results show impact of aflatoxin B-1 on multiple epigenetic modulations known to be pivotal in oncogenic processes.
机译:由机会真菌曲霉素生产的强迫性和阴险的继发性代谢物B-1,秉承毒物中间的杰出的地方,导致人类致命危害。黄曲霉毒素通过遗传和非遗传途径诱导多种效果来改变宿主细胞的功能。表观遗传机制拖累了解这一过程中涉及的新机制和新机制。我们现在的工作旨在研究多个表观遗传调节剂的功能表达谱。 AFB I调节多种表观遗传调节剂,如DNA甲基转移酶(DMNT),种子改性酶和Polycomb蛋白。 AFB(1)以剂量依赖性方式提高基因和蛋白质水平的DNMTS表达。它显着降低了组蛋白乙酰转移酶(帽子)活性,随着组蛋白脱乙酰化酶(HDAC)活性的显着增加以及剂量依赖性方式表达HDACS基因和蛋白质的诱导。多麦克力抑制蛋白B细胞特异性摩尼鼠白血病病毒整合位点1(BMI-1)和Zeste同源物2(EZH2)的增强剂的基因和蛋白表达显着结合H3K27的三甲基化和H2AK119的普发化。总之,我们的结果表明,黄曲霉毒素B-1对已知在致癌过程中枢转的多种表观遗传调节的影响。

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