Hai Tao, Yeung Man-Lung, Wood Thomas G, Wei Yuanfen, Yamaoka Shoji, Gatalica Zoran, Jeang Kuan-Teh, Brasier Allan R
Department of Internal Medicine, The University of Texas Medical Branch, 301 University Blvd., Galveston, Texas 77555-1060, USA.
J Virol. 2006 May;80(9):4227-41. doi: 10.1128/JVI.80.9.4227-4241.2006.
NF-kappaB is an inducible transcription factor mediating innate immune responses whose activity is controlled by the multiprotein IkappaB kinase (IKK) "signalsome". The core IKK consists of two catalytic serine kinases, IKKalpha and IKKbeta, and a noncatalytic subunit, IKKgamma. IKKgamma is required for IKK activity by mediating kinase oligomerization and serving to couple the core catalytic subunits to upstream mitogen-activated protein 3-kinase cascades. We have discovered an alternatively spliced IKKgamma mRNA isoform, encoding an in-frame deletion of exon 5, termed IKKgamma-delta. Using a specific reverse transcription-PCR assay, we find that IKKgamma-delta is widely expressed in cultured human cells and normal human tissues. Because IKKgamma-Delta protein is lacking a critical coiled-coil domain important in protein-protein interactions, we sought to determine its signaling properties by examining its ability to self associate, couple to activators of the canonical pathway, and mediate human T-cell leukemia virus type 1 (HTLV-1) Tax-induced NF-kappaB activity. Coimmunoprecipitation and confocal colocalization assays indicate IKKgamma-delta has strong homo- and heterotypic association with wild-type (WT) IKKgamma and, like IKKgamma WT, associates with the IKKbeta kinase. Similarly, IKKgamma-delta mediates IKK kinase activity and downstream NF-kappaB-dependent transcription in response to tumor necrosis factor (TNF) and the NF-kappaB-inducing kinase-IKKalpha signaling pathway. Surprisingly, however, in contrast to IKKgamma WT, IKKgamma-delta is not able to mediate HTLV-1 Tax-induced NF-kappaB-dependent transcription, even though IKKgamma-delta binds and colocalizes with Tax. These observations suggest that IKKgamma-delta is a functionally distinct alternatively spliced mRNA product differentially mediating TNF-induced, but not Tax-induced, signals converging on the IKK signalsome. Differing levels of IKKgamma-delta expression, therefore, may affect signal transduction cascades coupling to IKK.
核因子-κB是一种介导先天性免疫反应的可诱导转录因子,其活性受多蛋白IκB激酶(IKK)“信号体”的控制。核心IKK由两种催化丝氨酸激酶IKKα和IKKβ以及一个非催化亚基IKKγ组成。IKKγ通过介导激酶寡聚化并将核心催化亚基与上游丝裂原活化蛋白3激酶级联反应偶联来实现IKK活性。我们发现了一种选择性剪接的IKKγ mRNA异构体,其编码外显子5的框内缺失,称为IKKγ-δ。使用特异性逆转录-聚合酶链反应检测,我们发现IKKγ-δ在培养的人细胞和正常人体组织中广泛表达。由于IKKγ-δ蛋白缺乏在蛋白质-蛋白质相互作用中起关键作用的卷曲螺旋结构域,我们试图通过检测其自身缔合能力、与经典途径激活剂偶联能力以及介导人1型T细胞白血病病毒(HTLV-1)Tax诱导的核因子-κB活性来确定其信号特性。免疫共沉淀和共聚焦共定位检测表明,IKKγ-δ与野生型(WT)IKKγ有很强的同源和异源缔合,并且与IKKγ WT一样,与IKKβ激酶缔合。同样,IKKγ-δ介导IKK激酶活性以及响应肿瘤坏死因子(TNF)和核因子-κB诱导激酶-IKKα信号通路的下游核因子-κB依赖性转录。然而,令人惊讶的是,与IKKγ WT不同,即使IKKγ-δ与Tax结合并共定位,它也不能介导HTLV-1 Tax诱导的核因子-κB依赖性转录。这些观察结果表明,IKKγ-δ是一种功能上不同的选择性剪接mRNA产物,差异介导汇聚于IKK信号体的TNF诱导而非Tax诱导的信号。因此,不同水平的IKKγ-δ表达可能会影响与IKK偶联的信号转导级联反应。