Whiteside S T, Israël A
Unité de Biologie Moléculaire de l'Expression Génique, CNRS, Institut Pasteur, Paris, France.
Semin Cancer Biol. 1997 Apr;8(2):75-82. doi: 10.1006/scbi.1997.0058.
The Rel/NF-kappa B transcription factors represent the paradigm of regulation of transcriptional activation through sub-cellular localization. In unstimulated cells, NK-kappa B exists in an inactive state in the cytoplasm complexed to the inhibitory I kappa B molecules. Upon stimulation, I kappa B is rapidly degraded, freeing NF-kappa B to translocate to the nucleus and to activate the expression of its target genes. In this chapter, we will summarize what is known about the structure of I kappa B molecules, their functions, the mechanisms of I kappa B degradation, and the most common upstream signaling pathway (that is, serine phosphorylation) that leads to I kappa B degradation. Finally, we will discuss alternative mechanisms for induction of NF-kappa B through regulation of I kappa B activity.
Rel/NF-κB转录因子代表了通过亚细胞定位调控转录激活的范例。在未受刺激的细胞中,NF-κB以无活性状态存在于细胞质中,与抑制性IκB分子结合。受到刺激后,IκB迅速降解,使NF-κB得以转移至细胞核并激活其靶基因的表达。在本章中,我们将总结关于IκB分子的结构、功能、IκB降解机制以及导致IκB降解的最常见上游信号通路(即丝氨酸磷酸化)的已知信息。最后,我们将讨论通过调节IκB活性诱导NF-κB的其他机制。