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在诱导多能干细胞中miRNA - 5p和 - 3p种类的频繁共表达及交叉靶向作用

Frequent co-expression of miRNA-5p and -3p species and cross-targeting in induced pluripotent stem cells.

作者信息

Huang Chiu-Jung, Nguyen Phan Nguyen Nhi, Choo Kong Bung, Sugii Shigeki, Wee Kenneth, Cheong Soon Keng, Kamarul Tunku

机构信息

1. Department of Animal Science & Graduate Institute of Biotechnology, Chinese Culture University, Taipei, Taiwan;

2. Centre for Stem Cell Research, Universiti Tunku Abdul Rahman, Faculty of Medicine and Health Sciences, Kajang, Selangor, Malaysia;

出版信息

Int J Med Sci. 2014 Jun 5;11(8):824-33. doi: 10.7150/ijms.8358. eCollection 2014.

Abstract

BACKGROUND

A miRNA precursor generally gives rise to one major miRNA species derived from the 5' arm, and are called miRNA-5p. However, more recent studies have shown co-expression of miRNA-5p and -3p, albeit in different concentrations, in cancer cells targeting different sets of transcripts. Co-expression and regulation of the -5p and -3p miRNA species in stem cells, particularly in the reprogramming process, have not been studied.

METHODS

In this work, we investigated co-expression and regulation of miRNA-5p and -3p species in human induced pluripotent stem cells (iPSCs), mesenchymal stem cells (MSCs) and embryonic stem cells (ESC) using a nanoliter-scale real-time PCR microarray platform that included 1,036 miRNAs.

RESULTS

In comparing iPSC and ESC, only 32 miRNAs were found to be differentially expressed, in agreement of the ESC-like nature of iPSC. In the analysis of reprogramming process in iPSCs, 261 miRNAs were found to be differentially expressed compared with the parental MSC and pre-adipose tissue, indicating significant miRNA alternations in the reprogramming process. In iPSC reprogrammed from MSC, there were 88 miRNAs (33.7%), or 44 co-expressed 5p/3p pairs, clearly indicating frequent co-expression of both miRNA species on reprogramming. Of these, 40 pairs were either co-up- or co-downregulated indicating concerted 5p/3p regulation. The 5p/3p species of only 4 pairs were regulated in reverse directions. Furthermore, some 5p/3p species of the same miRNAs were found to target the same transcript and the same miRNA may cross-target different transcripts of proteins of the G1/S transition of the cell cycle; 5p/3p co-targeting was confirmed in stem-loop RT-PCR.

CONCLUSION

The observed cross- and co-regulation by paired miRNA species suggests a fail-proof scheme of miRNA regulation in iPSC, which may be important to iPSC pluripotency.

摘要

背景

微小RNA(miRNA)前体通常会产生一种主要来源于5'臂的miRNA,称为miRNA - 5p。然而,最近的研究表明,在癌细胞中,miRNA - 5p和 - 3p会共同表达,尽管浓度不同,且靶向不同的转录本组。干细胞中 - 5p和 - 3p miRNA种类的共同表达和调控,尤其是在重编程过程中,尚未得到研究。

方法

在这项研究中,我们使用包含1036种miRNA的纳升规模实时PCR微阵列平台,研究了人诱导多能干细胞(iPSC)、间充质干细胞(MSC)和胚胎干细胞(ESC)中miRNA - 5p和 - 3p种类的共同表达和调控。

结果

比较iPSC和ESC时,仅发现32种miRNA差异表达,这与iPSC的ESC样性质相符。在分析iPSC的重编程过程时,发现与亲本MSC和前脂肪组织相比,有261种miRNA差异表达,表明重编程过程中存在显著的miRNA变化。在由MSC重编程而来的iPSC中,有88种miRNA(33.7%),即44对共表达的5p/3p对,清楚地表明在重编程过程中这两种miRNA种类频繁共同表达。其中,40对要么共同上调,要么共同下调,表明5p/3p协同调控。只有4对的5p/3p种类呈反向调控。此外,发现一些相同miRNA的5p/3p种类靶向相同的转录本,并且相同的miRNA可能交叉靶向细胞周期G1/S转换蛋白的不同转录本;在茎环RT - PCR中证实了5p/3p共同靶向。

结论

观察到的配对miRNA种类的交叉调控和协同调控表明iPSC中存在一种可靠的miRNA调控机制,这可能对iPSC的多能性很重要。

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