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后生动物模型中 miRNA 靶调控的原理。

Principles of miRNA-target regulation in metazoan models.

机构信息

Basic Neurosciences Division, Biomedical Research Foundation of the Academy of Athens, Soranou Efesiou 4, Athens 11527, Greece.

出版信息

Int J Mol Sci. 2013 Aug 7;14(8):16280-302. doi: 10.3390/ijms140816280.

DOI:10.3390/ijms140816280
PMID:23965954
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3759911/
Abstract

MicroRNAs (miRs) are key post-transcriptional regulators that silence gene expression by direct base pairing to target sites of RNAs. They have a wide variety of tissue expression patterns and are differentially expressed during development and disease. Their activity and abundance is subject to various levels of control ranging from transcription and biogenesis to miR response elements on RNAs, target cellular levels and miR turnover. This review summarizes and discusses current knowledge on the regulation of miR activity and concludes with novel non-canonical functions that have recently emerged.

摘要

微小 RNA(miRs)是关键的转录后调控因子,通过与 RNA 靶位点的直接碱基配对来沉默基因表达。它们在组织中有广泛的表达模式,并在发育和疾病过程中表现出不同的表达。它们的活性和丰度受到各种水平的控制,包括转录和生物发生,以及 RNA 上的 miR 反应元件、靶细胞水平和 miR 周转率。本综述总结并讨论了 miR 活性的调控的最新知识,并以最近出现的新型非经典功能结束。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/f0d5c284e475/ijms-14-16280f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/914c4555b721/ijms-14-16280f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/61e919062f38/ijms-14-16280f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/f0d5c284e475/ijms-14-16280f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/914c4555b721/ijms-14-16280f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/61e919062f38/ijms-14-16280f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0a/3759911/f0d5c284e475/ijms-14-16280f3.jpg

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Nucleic Acids Res. 2013 Jul;41(13):6568-76. doi: 10.1093/nar/gkt361. Epub 2013 May 9.
2
ADAR1 forms a complex with Dicer to promote microRNA processing and RNA-induced gene silencing.ADAR1 与 Dicer 形成复合物,促进 microRNA 加工和 RNA 诱导的基因沉默。
Cell. 2013 Apr 25;153(3):575-89. doi: 10.1016/j.cell.2013.03.024.
3
Deciphering the rules of ceRNA networks.解读ceRNA网络的规则。
Adv Genet (Hoboken). 2022 Nov 26;3(4):2200026. doi: 10.1002/ggn2.202200026. eCollection 2022 Dec.
4
Neuronal microRNAs safeguard ER Ca homeostasis and attenuate the unfolded protein response upon stress.神经元 microRNAs 保护内质网 Ca2+ 稳态,并在应激时减弱未折叠蛋白反应。
Cell Mol Life Sci. 2022 Jun 21;79(7):373. doi: 10.1007/s00018-022-04398-9.
5
Protection by microRNA-7a-5p Antagomir Against Intestinal Mucosal Injury Related to the JNK Pathway in TNBS-Induced Experimental Colitis.microRNA-7a-5p 反义核苷酸对 JNK 通路相关的实验性结肠炎肠黏膜损伤的保护作用。
Turk J Gastroenterol. 2021 May;32(5):431-436. doi: 10.5152/tjg.2021.20746.
6
Validation of differentially expressed brain-enriched microRNAs in the plasma of PD patients.验证 PD 患者血浆中差异表达的脑富集 microRNAs。
Ann Clin Transl Neurol. 2020 Sep;7(9):1594-1607. doi: 10.1002/acn3.51146. Epub 2020 Aug 29.
7
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Eur Heart J. 2020 Jul 7;41(26):2453-2455. doi: 10.1093/eurheartj/ehaa444.
8
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4
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6
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7
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