Li C C, Dai R M, Chen E, Longo D L
Biological Carcinogenesis and Development Program, Program Resources, Inc./Dyncorp, Frederick, Maryland.
J Biol Chem. 1994 Dec 2;269(48):30089-92.
We have previously shown that NF-kappa B/Rel family members are physically associated phosphoproteins, and p105 and p50 are hyperphosphorylated after NF-kappa B activation. In this report, we further studied the phosphorylation involved in NF-kappa B activation in Jurkat T cells responding to phorbol 12-myristate 13-acetate and phytohemagglutinin. Immediately following stimulation, p50 is hyperphosphorylated, and a phosphorylated form of p50 (pp50) is translocated from the cytoplasm to the nucleus. The kinetics of this nuclear translocation paralleled that of the appearance of an active kappa B DNA-binding complex. An at least 30-fold higher level of kappa B DNA binding was detected in pp50 than p50. The enhanced binding could be attributed to a much greater stability detected in the complex consisting of kappa B DNA and pp50, but not p50. These results suggest that phosphorylation of p50, and perhaps other family members as well, may be involved in the activation of NF-kappa B/Rel family transcription factors.
我们之前已经表明,NF-κB/Rel家族成员是物理相关的磷蛋白,并且在NF-κB激活后p105和p50会发生过度磷酸化。在本报告中,我们进一步研究了佛波酯12-肉豆蔻酸酯13-乙酸酯和植物血凝素刺激的Jurkat T细胞中NF-κB激活所涉及的磷酸化。刺激后立即,p50发生过度磷酸化,并且磷酸化形式的p50(pp50)从细胞质转运到细胞核。这种核转运的动力学与活性κB DNA结合复合物的出现动力学平行。在pp50中检测到的κB DNA结合水平比p50至少高30倍。增强的结合可归因于在由κB DNA和pp50组成的复合物中检测到的更高稳定性,而不是p50。这些结果表明,p50以及可能其他家族成员的磷酸化可能参与NF-κB/Rel家族转录因子的激活。