plc - β1 MiRNA在疾病中的新作用

I. Faenza, L. Cocco
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引用次数: 1

摘要

核肌苷是独立调控的,其调控完全独立于质膜,这表明核构成了一个功能独特的肌醇脂代谢室。这表明核肌醇脂类本身可以调节转录和mrna前剪接、生长、增殖、细胞周期调节和分化等重要的核过程。磷脂酶Cβ1 (PLCβ1)是核肌苷信号转导的关键分子。最近有研究强调,在红细胞生成过程中,PLCβ1的作用与miR-210的作用有关。此外,PLCβ1信号传导与基因调控有关,并且随着PLCβ1的表达,microrna (mirna)发生变化。已发现PLCβ1的分子靶点在肌肉发生和造血过程中起重要作用。此外,PLCβ1信号传导已被证明在影响肌源性分化和影响造血系统的疾病中受损。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging role for PLCβ1 MiRNA and disease
Nuclear inositides are independently regulated and their regulation is totally independent from the plasma membrane counterpart, suggesting that the nucleus constitutes a functionally distinct compartment of inositol lipids metabolism. This suggests that nuclear inositol lipids themselves can modulate nuclear processes as important as transcription and pre-mRNA splicing, growth, proliferation, cell cycle regulation and differentiation. Phospholipase C β1 (PLCβ1) is a key molecule for nuclear inositide signaling. Very recently it has been highlighted that the role of PLCβ1 during erythropoiesis is linked to that of miR-210. Moreover PLCβ1 signaling is linked to gene regulation and changes in microRNAs (miRNAs) occurs with PLCβ1 expression. Molecular targets of PLCβ1 have been found to be important during myogenesis and hematopoiesis. In addition, PLCβ1 signaling has been demonstrated to be impaired in diseases affecting both myogenic differentiation and affecting the hematopoietic system.
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