人核受体亚细胞定位的综合分析与预测

Samatha Mathew, Keshav Thakur, Sudhir Kumar, A. Yende, Shashi Singh, A. K. Dash, R. Tyagi
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引用次数: 4

摘要

核受体(NR)超家族由保守的配体调节的细胞内转录因子组成,这些因子在其同源配体存在的情况下激活过多的信号网络,从而开始其各自的转录功能。所有NRs在连接物或活性时都是核的。然而,当未发光或无活性时,它们在细胞核和细胞质之间的定位可能不同。NRs控制着身体从新陈代谢到繁殖和发育的大部分生理过程。到目前为止,在人类的情况下,已经鉴定出48个NRs,它们定位在细胞的胞质、细胞核或两个隔室中。蛋白质的亚细胞定位与其功能密切相关。然而,人类NRs的特定亚细胞定位模式充满了模糊性,并且大多充满了争议,只有少数NRs在特定的生理条件下得到了很好的研究和建立。在本研究中,我们试图弥合这一差距,并试图根据已发表的实验数据和计算机预测方法,得出与人类NRs亚细胞定位有关的结论。这种全面的分析不仅有助于得出关于它们对生理过程的控制的结论,而且可能为理解NR介导的疾病的分子基础开辟新的途径,这些疾病归因于它们的定位错误和功能失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comprehensive Analysis and Prediction of Sub-Cellular Localization of Human Nuclear Receptors
The Nuclear Receptor (NR) superfamily comprises of conserved ligand-modulated intracellular transcription factors which in the presence of their cognate ligands activate a plethora of signaling networks, thereby commencing their respective transcription functions. All NRs are nuclear when liganded or active. However, their localization may differ between nucleus and cytoplasm when unliganded or inactive. NRs control a majority of physiological processes in body ranging from metabolism to reproduction and development. Hitherto, in case of humans, 48 NRs have been identified which are localized either in cytosolic, nuclear or both compartments of the cell. Sub-cellular localization of proteins has great relevance in relation to their function. However, specific sub-cellular localization patterns of human NRs are clouded with ambiguity and are mostly ridden with controversy, with only a few of them being well-studied and established under specific physiological conditions. In the present study, we attempted to bridge the gap and attempted to draw conclusions in relation to sub-cellular localization of human NRs based on published experimental data and by in-silico prediction methods. This comprehensive analysis may not only be useful to draw conclusions on their control of physiological processes but may also open new avenues towards understanding of the molecular basis of NR-mediated diseases attributed to their mislocalization and malfunctioning.
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