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首页> 外文期刊>Mutation Research - Genetic Toxicology and Environmental Mutagenesis >MiR-34a suppresses mutagenesis by inducing apoptosis in human lymphoblastoid TK6 cells
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MiR-34a suppresses mutagenesis by inducing apoptosis in human lymphoblastoid TK6 cells

机译:MiR-34a通过诱导人淋巴母细胞TK6细胞凋亡来抑制诱变

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miRNA precursors and inhibitors have been used to modulate the expression of their targeted mRNA and thereby study miRNA functions. We indicated in our previous work that X-ray induces miR-34a expression in a time and dose dependent manner. The objective of this study was to elucidate the role of miR-34a in X-ray-induced mutations in human lymphoblast TK6 cells. Neither over-expression of miR-34a by lipid transfection of miR-34a precursor nor down regulation of endogenous miR-34a by miR-34a inhibitor had any effect on X-ray-induced micronucleus frequency in TK6 cells. Over-expression of miR-34a in TK6 cells significantly reduced X-ray induced mutant frequency (MF) in the Thymidine Kinase ( TK) locus while suppression of endogenous miR-34a can increase the background level MF in TK6 cells. Furthermore, over-expression of miR-34a promoted and down-regulation of miR-34a inhibited background and X-ray-induced apoptosis in TK6 cells. Our study suggests miR-34a is an important negative regulator of mutagenesis and the mechanism is possibly mediated through apoptosis.
机译:miRNA前体和抑制剂已用于调节其靶向mRNA的表达,从而研究miRNA的功能。我们在以前的工作中指出,X射线以时间和剂量依赖性方式诱导miR-34a表达。这项研究的目的是阐明miR-34a在X射线诱导的人淋巴母细胞TK6细胞突变中的作用。 miR-34a前体的脂质转染导致miR-34a的过表达或miR-34a抑制剂对内源性miR-34a的下调都没有影响TK6细胞中X射线诱导的微核频率。 TK6细胞中miR-34a的过表达显着降低了胸苷激酶(TK)基因座中X射线诱导的突变频率(MF),而内源性miR-34a的抑制可增加TK6细胞中的背景水平MF。此外,miR-34a的过表达促进了miR-34a的下调抑制了TK6细胞的背景和X射线诱导的凋亡。我们的研究表明,miR-34a是诱变的重要负调控因子,其机制可能是通过凋亡介导的。

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