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囊性纤维化跨膜传导调节因子作为一种表观遗传调节因子的新作用:将环境线索与微小RNA联系起来。

Emerging role of cystic fibrosis transmembrane conductance regulator as an epigenetic regulator: linking environmental cues to microRNAs.

作者信息

Chan Hsiao Chang, Jiang Xiaohua, Ruan Ye Chun

机构信息

Faculty of Medicine, Epithelial Cell Biology Research Center, Key Laboratory for Regenerative Medicine of Ministry of Education of China, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.

出版信息

Clin Exp Pharmacol Physiol. 2014 Sep;41(9):615-22. doi: 10.1111/1440-1681.12271.

DOI:10.1111/1440-1681.12271
PMID:24909068
Abstract

Although microRNAs (miRNAs) have been recognized as one of the important epigenetic mechanisms that regulate gene expression in response to changes in the environment, the links between environmental cues and changes in miRNAs remain largely unknown. Localized to the cell membrane and recognized as an anion channel, the cystic fibrosis transmembrane conductance regulator (CFTR) has recently been shown to mediate important signalling pathways leading to activation of miRNAs. This brief review summarizes the related findings and discusses the emerging role of CFTR as an epigenetic regulator, possibly involved in a wide spectrum of physiological and pathological processes.

摘要

尽管微小RNA(miRNA)已被公认为是一种重要的表观遗传机制,可响应环境变化调节基因表达,但环境线索与miRNA变化之间的联系仍 largely unknown。囊性纤维化跨膜传导调节因子(CFTR)定位于细胞膜,被认为是一种阴离子通道,最近已被证明可介导导致miRNA激活的重要信号通路。本简要综述总结了相关发现,并讨论了CFTR作为一种表观遗传调节因子的新作用,其可能参与广泛的生理和病理过程。

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Emerging role of cystic fibrosis transmembrane conductance regulator as an epigenetic regulator: linking environmental cues to microRNAs.囊性纤维化跨膜传导调节因子作为一种表观遗传调节因子的新作用:将环境线索与微小RNA联系起来。
Clin Exp Pharmacol Physiol. 2014 Sep;41(9):615-22. doi: 10.1111/1440-1681.12271.
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MicroRNAs and cystic fibrosis--an epigenetic perspective.微小 RNA 与囊性纤维化——表观遗传学视角。
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Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.miRNA-145、-223 和 -494 对囊性纤维化跨膜电导调节因子的调控在 ΔF508 囊性纤维化气道上皮细胞中发生改变。
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Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.囊性纤维化跨膜传导调节因子氯离子和碳酸氢根离子传导的选择性激活。
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MicroRNA regulation of expression of the cystic fibrosis transmembrane conductance regulator gene.微小 RNA 对囊性纤维化跨膜电导调节因子基因表达的调控。
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Cystic fibrosis transmembrane conductance regulator (CFTR) nucleotide-binding domain 1 (NBD-1) and CFTR truncated within NBD-1 target to the epithelial plasma membrane and increase anion permeability.囊性纤维化跨膜传导调节因子(CFTR)核苷酸结合结构域1(NBD-1)以及在NBD-1内截短的CFTR定位于上皮细胞质膜并增加阴离子通透性。
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The cystic fibrosis transmembrane regulator forms macromolecular complexes with PDZ domain scaffold proteins.囊性纤维化跨膜传导调节因子与PDZ结构域支架蛋白形成大分子复合物。
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