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核因子-κB调控抑制蛋白IκBα的表达:诱导性自身调节途径的证据

NF-kappa B controls expression of inhibitor I kappa B alpha: evidence for an inducible autoregulatory pathway.

作者信息

Sun S C, Ganchi P A, Ballard D W, Greene W C

机构信息

Gladstone Institute of Virology and Immunology, University of California, San Francisco.

出版信息

Science. 1993 Mar 26;259(5103):1912-5. doi: 10.1126/science.8096091.

Abstract

The eukaryotic transcription factor nuclear factor-kappa B (NF-kappa B) participates in many parts of the genetic program mediating T lymphocyte activation and growth. Nuclear expression of NF-kappa B occurs after its induced dissociation from its cytoplasmic inhibitor I kappa B alpha. Phorbol ester and tumor necrosis factor-alpha induction of nuclear NF-kappa B is associated with both the degradation of performed I kappa B alpha and the activation of I kappa B alpha gene expression. Transfection studies indicate that the I kappa B alpha gene is specifically induced by the 65-kilodalton transactivating subunit of NF-kappa B. Association of the newly synthesized I kappa B alpha with p65 restores intracellular inhibition of NF-kappa B DNA binding activity and prolongs the survival of this labile inhibitor. Together, these results show that NF-kappa B controls the expression of I kappa B alpha by means of an inducible autoregulatory pathway.

摘要

真核转录因子核因子-κB(NF-κB)参与介导T淋巴细胞激活和生长的遗传程序的多个环节。NF-κB从其细胞质抑制剂IκBα诱导解离后发生核表达。佛波酯和肿瘤坏死因子-α诱导核NF-κB与已有的IκBα降解以及IκBα基因表达激活均相关。转染研究表明,IκBα基因由NF-κB的65千道尔顿反式激活亚基特异性诱导。新合成的IκBα与p65结合可恢复细胞内对NF-κB DNA结合活性的抑制,并延长这种不稳定抑制剂的存活时间。这些结果共同表明,NF-κB通过可诱导的自调节途径控制IκBα的表达。

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