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The nuclear transportation routes of membrane-bound transcription factors

机译:膜结合转录因子的核转运途径

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摘要

Membrane-bound transcription factors (MTFs) are transcription factors (TFs) that are anchored in membranes in a dormant state. Activated by external or internal stimuli, MTFs are released from parent membranes and are transported to the nucleus. Existing research indicates that some plasma membrane (PM)-bound proteins and some endoplasmic reticulum (ER) membrane-bound proteins have the ability to enter the nucleus. Upon specific signal recognition cues, some PM-bound TFs undergo proteolytic cleavage to liberate the intracellular fragments that enter the nucleus to control gene transcription. However, lipid-anchored PM-bound proteins enter the nucleus in their full length for depalmitoylation. In addition, some PM-bound TFs exist as full-length proteins in cell nucleus via trafficking to the Golgi and the ER, where membrane-releasing mechanisms rely on endocytosis. In contrast, the ER membrane-bound TFs relocate to the nucleus directly or by trafficking to the Golgi. In both of these pathways, only the fragments of the ER membrane-bound TFs transit to the nucleus. Several different nuclear trafficking modes of MTFs are summarized in this review, providing an effective supplement to the mechanisms of signal transduction and gene regulation. Moreover, targeting intracellular movement pathways of disease-associated MTFs may significantly improve the survival of patients.
机译:膜结合转录因子(MTFs)是以休眠状态锚定在膜中的转录因子(TFs)。通过外部或内部刺激激活,MTF从母膜释放并转运至细胞核。现有研究表明,某些质膜(PM)结合蛋白和某些内质网(ER)膜结合蛋白具有进入细胞核的能力。根据特定的信号识别提示,一些与PM结合的TF进行蛋白水解切割,以释放进入细胞核以控制基因转录的细胞内片段。然而,脂质锚定的PM结合蛋白以其全长进入去核化的核。另外,一些PM结合的TFs通过转运到高尔基体和ER而以全长蛋白的形式存在于细胞核中,其中膜的释放机制依赖于内吞作用。相反,结合ER膜的TF直接或通过转运至高尔基体而重新定位至细胞核。在这两种途径中,仅ER膜结合的TF的片段转移至细胞核。这篇综述总结了几种不同的MTF核贩运模式,为信号转导和基因调控机制提供了有效的补充。而且,靶向与疾病相关的MTF的细胞内运动途径可以显着提高患者的存活率。

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