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首页> 外文期刊>DNA and Cell Biology >Differential Expression of miR-202 and Validation of Predicted Target Genes in the Skin Tissue of C57BL/6 Black Mice and BALB/c White Mice
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Differential Expression of miR-202 and Validation of Predicted Target Genes in the Skin Tissue of C57BL/6 Black Mice and BALB/c White Mice

机译:miR-202的差异表达及验证C57BL / 6黑小鼠皮肤组织中的预测靶基因及BALB / C白老鼠

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In recent years, with the need of the fur industry to obtain greater quantities of high-quality fur and the research of hair follicle development attracting greater attention, the role of miRNAs in hair follicle development has become a field of intense interest. miRNAs are short length RNAs that affect gene regulation by binding to the 3'-untranslated region (3'UTR) of the mRNAs of certain target genes. This study predicted and validated the target genes of miR-202 in the skin tissue of C57BL/6 black mice and BALB/c white mice. The expression of miR-202 target genes (wnt5a, kit, and tcf7) was examined by real-time quantitative polymerase chain reaction and western blot in the mouse skin tissue and human embryonic kidney 293T cells (HEK293T cells) which overexpress miR-202. The luciferase reporter gene system was used to verify the correlation between the expression of miR-202 and its putative target genes. We show that the expression of miR-202 was higher in the skin tissue of C57BL/6 black mice than in the skin tissue of BALB/c white mice (p 0.05). Furthermore, the expression of wnt5a, kit, and tcf7 was observed to be negatively correlated with the expression of miR-202 and to be downregulated by miR-202 in vitro and in vivo. The luciferase reporter gene system indicated that the target sequences of miR-202 are present in 3'UTR of wnt5a, kit, and tcf7 mRNAs. Altogether, this study has shown that the expression of miR-202 was different in the skin tissue of C57BL/6 black mice and BALB/c white mice and that wnt5a, kit, and tcf7 are negatively regulated by miR-202.
机译:近年来,随着毛皮行业对获取更多优质毛皮的需求以及毛囊发育的研究越来越受到关注,miRNA在毛囊发育中的作用已成为一个备受关注的领域。miRNA是短长度RNA,通过与特定靶基因的mRNA的3'非翻译区(3'UTR)结合而影响基因调控。本研究预测并验证了C57BL/6黑小鼠和BALB/c白小鼠皮肤组织中miR-202的靶基因。通过实时定量聚合酶链反应和western blot检测小鼠皮肤组织和过度表达miR-202的人类胚胎肾293T细胞(HEK293T细胞)中miR-202靶基因(wnt5a、kit和tcf7)的表达。荧光素酶报告基因系统用于验证miR-202的表达与其假定的靶基因之间的相关性。我们发现,在C57BL/6黑小鼠的皮肤组织中,miR-202的表达高于BALB/c白小鼠的皮肤组织(p;0.05)。此外,观察到wnt5a、kit和tcf7的表达与miR-202的表达呈负相关,并在体外和体内被miR-202下调。荧光素酶报告基因系统表明,miR-202的靶序列存在于wnt5a、kit和tcf7 mRNA的3’UTR中。总之,本研究表明,miR-202在C57BL/6黑小鼠和BALB/c白小鼠的皮肤组织中的表达不同,wnt5a、kit和tcf7受到miR-202的负调控。

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