Scott M L, Fujita T, Liou H C, Nolan G P, Baltimore D
Rockefeller University, New York, New York 10021.
Genes Dev. 1993 Jul;7(7A):1266-76. doi: 10.1101/gad.7.7a.1266.
Transcription factor NF-kappa B (p50/p65) is generally localized to the cytoplasm by its inhibitor I kappa B. Overproduced I kappa B, free from NF-kappa B, is rapidly degraded. Overexpression of p65 increases endogenous I kappa B protein in both carcinoma and lymphoid cells by two mechanisms: protein stabilization and increased transcription of I kappa B mRNA. In contrast, p65 delta, a naturally occurring splice variant, fails to markedly augment I kappa B protein levels. Both overexpressed p65 and coexpressed p50 are cytoplasmic, whereas p65 delta is partly nuclear, indicating that the I kappa B induced by p65 can maintain NF-kappa B in the cytoplasm. Thus, p65 and I kappa B are linked in an autoregulatory loop, ensuring that NF-kappa B is held in the cytoplasm until cells are specifically induced to translocate it to the nucleus.
转录因子核因子-κB(p50/p65)通常通过其抑制剂IκB定位于细胞质中。过量产生的、与核因子-κB分离的IκB会迅速降解。p65的过表达通过两种机制增加癌细胞和淋巴细胞中的内源性IκB蛋白:蛋白质稳定化和IκB mRNA转录增加。相比之下,天然存在的剪接变体p65δ未能显著提高IκB蛋白水平。过表达的p65和共表达的p50都位于细胞质中,而p65δ部分位于细胞核中,这表明p65诱导产生的IκB可以将核因子-κB维持在细胞质中。因此,p65和IκB通过一个自动调节环相连,确保核因子-κB保持在细胞质中,直到细胞被特异性诱导将其转运到细胞核。