Aoki T, Sano Y, Yamamoto T, Inoue J I
Department of Oncology, The Institute of Medical Science, The University of Tokyo, Japan.
Oncogene. 1996 Mar 7;12(5):1159-64.
The nuclear activity of Rel/NFkappaB transcription factors is tightly regulated from the cytoplasmic compartment by an inhibitory subunit called IkappaBalpha. IkappaBalpha is rapidly phosphorylated and degraded in response to the stimulation through tumor necrosis factor alpha (TNFalpha) receptor, interleukin-1 receptor or CD40. To explore the molecular mechanisms of signal-induced depletion of IkappaBalpha, we have delineated the domain in IkappaBalpha that is required for TNFalpha-induced phosphorylation and rapid degradation of IkappaBalpha. In contrast to the previous reports, the PEST-like sequences, which are present in the carboxyl-terminal region of IkappaBalpha, are demonstrated here to be dispensable for TNFalpha-induced degradation but could be required for signal-independent degradation, as in the case of Cactus, Drosophila homologue of IkappaB. Furthermore, the ankyrin repeats, which are essential for forming a complex with Rel and RelA, are required for TNFalpha-induced degradation suggesting that the putative IkappaB protease could interact with IkappaBalpha in complex with RelA or could recognize the structure of ankyrin repeats. Our data also indicate that neither the ankyrin repeats nor the PEST-like sequences, are essential for TNFalpha-induced phosphorylation.
Rel/NFκB转录因子的核活性由一种名为IκBα的抑制性亚基在细胞质区室中受到严格调控。IκBα在通过肿瘤坏死因子α(TNFα)受体、白细胞介素-1受体或CD40刺激后会迅速磷酸化并降解。为了探究信号诱导的IκBα耗竭的分子机制,我们已经确定了IκBα中TNFα诱导的IκBα磷酸化和快速降解所需的结构域。与之前的报道相反,IκBα羧基末端区域存在的类PEST序列在这里被证明对于TNFα诱导的降解是可有可无的,但对于信号非依赖性降解可能是必需的,就像IκB的果蝇同源物仙人掌蛋白的情况一样。此外,对于与Rel和RelA形成复合物至关重要的锚蛋白重复序列,对于TNFα诱导的降解是必需的,这表明假定的IκB蛋白酶可以与与RelA结合的IκBα相互作用,或者可以识别锚蛋白重复序列的结构。我们的数据还表明,锚蛋白重复序列和类PEST序列对于TNFα诱导的磷酸化都不是必需的。