Role of MiRNA in the Regulation of Blood Group Expression

R. Kronstein-Wiedemann, Stephan R. Künzel, Jessica Thiel, Torsten Tonn
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Abstract

Background: MicroRNAs (miRNAs) are small, endogenous non-coding RNA molecules that inhibit gene expression through either destabilization of the target mRNA or translational repression. MiRNAs recognize target sites, most commonly found in the 3′-untranslated regions of cognate mRNAs. This review aims to provide a state-of-the-art overview of the role of miRNAs in the regulation of major blood group antigens such as ABH as well as cancer-specific glycans. Summary: Besides their known roles in the control of developmental processes, proliferation, apoptosis, and carcinogenesis, miRNAs have recently been identified to play a regulatory role during erythropoiesis and blood group antigen expression. Since only little is known about the function of the red cell membrane proteins carrying blood group antigens, it is of great interest to shed light on the regulatory mechanisms of blood group gene expression. Some carrier proteins of blood group antigens are not restricted to red blood cells and are widely expressed in other bodily fluids and tissues and quite a few play a crucial role in tumor cells, as either tumor suppressors or promoters. Key Message: All available data point at a tremendous physiological as well as pathophysiological relevance of miRNAs in context of blood group regulation. Furthermore, miRNAs are involved in the regulation of pleiotropic genetic pathways such as hematopoiesis and tumorigenesis and thus have to be studied in future research on this subject.
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MiRNA 在调控血型表达中的作用
背景:微小RNA(miRNA)是一种小型内源性非编码RNA分子,可通过破坏目标mRNA的稳定性或抑制翻译来抑制基因表达。MiRNA 可识别目标位点,这些位点通常位于同源 mRNA 的 3′-非翻译区。本综述旨在概述 miRNA 在调控 ABH 等主要血型抗原以及癌症特异性聚糖方面的作用。摘要:除了在控制发育过程、增殖、凋亡和癌变方面的已知作用外,最近还发现 miRNA 在红细胞生成和血型抗原表达过程中发挥调控作用。由于人们对携带血型抗原的红细胞膜蛋白的功能知之甚少,因此揭示血型基因表达的调控机制非常有意义。血型抗原的一些载体蛋白并不局限于红细胞,它们在其他体液和组织中也广泛表达,其中有不少在肿瘤细胞中发挥着重要作用,既是肿瘤抑制因子,也是肿瘤促进因子。关键信息:所有现有数据都表明,miRNA 在血型调节方面具有巨大的生理和病理生理学意义。此外,miRNAs 还参与调节造血和肿瘤发生等多有害基因通路,因此必须在今后的相关研究中加以研究。
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