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由HER2编码的miR-4728-3p通过非经典内部种子序列相互作用调控ESR1。

The HER2-encoded miR-4728-3p regulates ESR1 through a non-canonical internal seed interaction.

作者信息

Newie Inga, Søkilde Rolf, Persson Helena, Grabau Dorthe, Rego Natalia, Kvist Anders, von Stedingk Kristoffer, Axelson Håkan, Borg Åke, Vallon-Christersson Johan, Rovira Carlos

机构信息

BioCare, Strategic Cancer Research Program, Lund, Sweden; Department of Oncology and Pathology, Lund University Cancer Center, Lund, Sweden.

Department of Oncology and Pathology, Lund University Cancer Center, Lund, Sweden.

出版信息

PLoS One. 2014 May 14;9(5):e97200. doi: 10.1371/journal.pone.0097200. eCollection 2014.

Abstract

Since the early 1980s remarkable progress has been made in understanding the role of the HER2 locus in carcinogenesis, but many details of its regulatory network are still elusive. We recently reported the finding of 367 new human microRNA (miRNA) genes of which one, mir-4728, is encoded in an intron of the HER2 gene. Here, we confirm that the HER2 oncogene is a bi-functional locus encoding the membrane receptor and a functional miRNA gene. We further show that miR-4728-3p has alternative functionalities depending on the region used for interaction with its target; the canonical seed between nucleotides 2-8 or a novel, more internal seed shifted to nucleotides 6-12. Analysis of public data shows that this internal seed region, although rare compared to the far more abundant canonical 2-8 seed interaction, can also direct targeted down-regulation by other miRNAs. Through the internal seed, miR-4728-3p regulates expression of estrogen receptor alpha, an interaction that would have remained undetected if classic rules for miRNA-target interaction had been applied. In summary, we present here an alternative mode of miRNA regulation and demonstrate this dual function of the HER2 locus, linking the two major biomarkers in breast cancer.

摘要

自20世纪80年代初以来,在理解HER2基因座在致癌作用中的作用方面已经取得了显著进展,但其调控网络的许多细节仍然难以捉摸。我们最近报告发现了367个新的人类微小RNA(miRNA)基因,其中一个mir-4728编码于HER2基因的一个内含子中。在此,我们证实HER2癌基因是一个双功能基因座,既编码膜受体,也编码一个功能性miRNA基因。我们进一步表明,miR-4728-3p根据与其靶标相互作用所使用的区域具有不同的功能;核苷酸2-8之间的典型种子序列或一个新的、更靠内部的种子序列,其位置转移到了核苷酸6-12。对公开数据的分析表明,尽管与丰富得多的典型2-8种子相互作用相比,这个内部种子区域较为罕见,但它也能指导其他miRNA进行靶向下调。通过内部种子序列,miR-4728-3p调节雌激素受体α的表达,如果应用miRNA-靶标相互作用的经典规则,这种相互作用可能仍未被发现。总之,我们在此展示了一种miRNA调控的替代模式,并证明了HER2基因座的这种双重功能,将乳腺癌中的两个主要生物标志物联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/108b/4020767/4201519a2124/pone.0097200.g001.jpg

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