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小鼠的束缚应激改变了一组25个调控与应激和抑郁相关mRNA的miRNA。

Restraint Stress in Mice Alters Set of 25 miRNAs Which Regulate Stress- and Depression-Related mRNAs.

作者信息

Solich Joanna, Kuśmider Maciej, Faron-Górecka Agata, Pabian Paulina, Dziedzicka-Wasylewska Marta

机构信息

Maj Institute of Pharmacology Polish Academy of Sciences, Smętna Street 12, 31-343 Kraków, Poland.

出版信息

Int J Mol Sci. 2020 Dec 12;21(24):9469. doi: 10.3390/ijms21249469.

Abstract

In the present study, we aim to identify the effect of restrain stress (RS) on the expression of miRNAs in mouse serum. We used three genotypes of animals (mice with knock-out of the gene-encoding norepinephrine transporter, ; , and ) which had previously been shown to display different sensitivity to RS, and focused on miRNAs which were altered by RS in the serum of all three genotypes. An analysis of miRNAs expression allowed for the identification of a set of 25 differentially expressed miRNAs; 10 were down-regulated compared to an appropriate control group of animals, while 15 were up-regulated. The application of DIANA-miRPath v. 3.0 allowed for the identification of selected pathways (KEGG) and Gene Ontology (GO) categories that were significantly controlled by these miRNAs, while miRWalk v. 3.0-the platform that used the machine learning based algorithm, TaRPmiR-was used to find their targets. The results indicate that 25 miRNAs, identified as altered upon RS in three genotypes of mice, are responsible for regulation of mRNA-encoding proteins that are key for the main hypotheses of depression; therefore, they may help to understand the link between stress and depression at the molecular level.

摘要

在本研究中,我们旨在确定束缚应激(RS)对小鼠血清中微小RNA(miRNA)表达的影响。我们使用了三种基因型的动物(编码去甲肾上腺素转运体的基因敲除小鼠, ; ,以及 ),这些动物先前已被证明对RS表现出不同的敏感性,并聚焦于在所有三种基因型小鼠血清中因RS而发生改变的miRNA。对miRNA表达的分析使得能够鉴定出一组25种差异表达的miRNA;与相应的动物对照组相比,10种miRNA表达下调,而15种miRNA表达上调。应用DIANA-miRPath v. 3.0能够鉴定出这些miRNA显著调控的特定通路(KEGG)和基因本体(GO)类别,而miRWalk v. 3.0——使用基于机器学习算法TaRPmiR的平台——则用于寻找它们的靶标。结果表明,在三种基因型小鼠中被鉴定为因RS而发生改变的25种miRNA,负责调控对抑郁症主要假说至关重要的编码蛋白质的mRNA;因此,它们可能有助于在分子水平上理解应激与抑郁症之间的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dd6/7763317/4e93904d6767/ijms-21-09469-g001a.jpg

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