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γ-Glutamyl hydrolase modulation significantly influences global and gene-specific DNA methylation and gene expression in human colon and breast cancer cells

机译:γ-谷氨酰水解酶的调节显着影响人类结肠癌和乳腺癌细胞中的全局和基因特异性DNA甲基化和基因表达

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摘要

γ-Glutamyl hydrolase (GGH) plays an important role in folate homeostasis by catalyzing hydrolysis of polyglutamylated folate into monoglutamates. Polyglutamylated folates are better substrates for several enzymes involved in the generation of S-adenosylmethionine, the primary methyl group donor, and hence, GGH modulation may affect DNA methylation. DNA methylation is an important epigenetic determinant in gene expression, in the maintenance of DNA integrity and stability, and in chromatin modifications, and aberrant or dysregulation of DNA methylation has been mechanistically linked to the development of human diseases including cancer. Using a recently developed in vitro model of GGH modulation in HCT116 colon and MDA-MB-435 breast cancer cells, we investigated whether GGH modulation would affect global and gene-specific DNA methylation and whether these alterations were associated with significant gene expression changes. In both cell lines, GGH overexpression decreased global DNA methylation and DNA methyltransferase (DNMT) activity, while GGH inhibition increased global DNA methylation and DNMT activity. Epigenomic and gene expression analyses revealed that GGH modulation influenced CpG promoter DNA methylation and gene expression involved in important biological pathways including cell cycle, cellular development, and cellular growth and proliferation. Some of the observed altered gene expression appeared to be regulated by changes in CpG promoter DNA methylation. Our data suggest that the GGH modulation-induced changes in total intracellular folate concentrations and content of long-chain folylpolyglutamates are associated with functionally significant DNA methylation alterations in several important biological pathways.Electronic supplementary materialThe online version of this article (doi:10.1007/s12263-014-0444-0) contains supplementary material, which is available to authorized users.
机译:γ-谷氨酰水解酶(GGH)通过催化多谷氨酰化叶酸水解成单谷氨酸盐而在叶酸体内平衡中发挥重要作用。多聚谷氨酰胺化叶酸是参与主要甲基供体S-腺苷甲硫氨酸生成的几种酶的较好底物,因此,GGH调节可能影响DNA甲基化。 DNA甲基化是基因表达,维持DNA完整性和稳定性以及染色质修饰中重要的表观遗传决定因素,而DNA甲基化的异常或失调已与人类疾病(包括癌症)的发生机制相关。使用最近开发的体外在HCT116结肠和MDA-MB-435乳腺癌细胞中GGH调节的模型,我们调查了GGH调节是否会影响整体和基因特异性DNA甲基化,以及这些改变是否与显着的基因表达变化相关。在两种细胞系中,GGH的过量表达均降低了总体DNA甲基化和DNA甲基转移酶(DNMT)的活性,而GGH的抑制则提高了总体DNA甲基化和DNMT的活性。表观基因组和基因表达分析表明,GGH调节影响CpG启动子DNA甲基化和基因表达,这些基因参与重要的生物途径,包括细胞周期,细胞发育以及细胞生长和增殖。观察到的某些基因表达改变似乎受CpG启动子DNA甲基化变化的调节。我们的数据表明,GGH调节诱导的总细胞内叶酸浓度和长链叶酰聚谷氨酸含量的变化与几种重要生物学途径中功能上显着的DNA甲基化改变有关。电子补充材料本文的在线版本(doi:10.1007 / s12263 -014-0444-0)包含补充材料,授权用户可以使用。

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