Dutta Jui, Fan Gaofeng, Gélinas Céline
CABM, 679 Hoes Lane, Piscataway, NJ 08854.
J Virol. 2008 Nov;82(21):10792-802. doi: 10.1128/JVI.00903-08. Epub 2008 Aug 27.
The Rel/NF-kappaB transcription factors are constitutively activated in many human cancers. The Rel proteins in this family are implicated in leukemia/lymphomagenesis, but the mechanism is not completely understood. Previous studies showed that the transcription activation domains (TADs) of the viral oncoprotein v-Rel and its cellular Rel/NF-kappaB homologues c-Rel and RelA are key determinants of their different transforming activities in primary lymphocytes. Substitution of a Rel TAD for that of RelA conferred a strong transforming phenotype upon RelA, which otherwise failed to transform cells. To gain insights into protein interactions that influence cell transformation by the Rel TADs, we identified factors that interact with the TAD of v-Rel, the most oncogenic member of the Rel/NF-kappaB family. We report that the coactivator for transcription factors AP-1 and estrogen receptors, CAPERalpha, interacts with the v-Rel TAD and potently synergizes v-Rel-mediated transactivation. Importantly, coexpression of CAPERalpha markedly reduced and delayed v-Rel's transforming activity in primary lymphocytes, whereas a dominant-negative mutant enhanced the kinetics of v-Rel-mediated transformation. Furthermore, small interfering RNA-mediated knockdown of CAPERalpha in v-Rel-transformed lymphocytes significantly enhanced colony formation in soft agar. Since the potency of Rel-mediated transactivation is an important determinant of lymphocyte transformation, as is Rel's ability to induce transcriptional repression, these data suggest that CAPERalpha's interaction with the Rel TAD could modulate Rel/NF-kappaB's transforming activity by facilitating expression or dampening repression of specific gene subsets important for oncogenesis. Overall, this study identifies CAPERalpha as a new transcriptional coregulator for v-Rel and reveals an important role in modulating Rel's oncogenic activity.
Rel/NF-κB转录因子在许多人类癌症中被组成性激活。该家族中的Rel蛋白与白血病/淋巴瘤的发生有关,但其机制尚未完全明确。先前的研究表明,病毒癌蛋白v-Rel及其细胞Rel/NF-κB同源物c-Rel和RelA的转录激活域(TAD)是它们在原代淋巴细胞中不同转化活性的关键决定因素。用Rel的TAD替换RelA的TAD可赋予RelA强大的转化表型,否则RelA无法转化细胞。为了深入了解影响Rel TAD介导的细胞转化的蛋白质相互作用,我们鉴定了与Rel/NF-κB家族中最具致癌性的成员v-Rel的TAD相互作用的因子。我们报告说,转录因子AP-1和雌激素受体的共激活因子CAPERα与v-Rel的TAD相互作用,并有力地协同v-Rel介导的反式激活。重要的是,CAPERα的共表达显著降低并延迟了v-Rel在原代淋巴细胞中的转化活性,而显性负性突变体则增强了v-Rel介导的转化动力学。此外,在v-Rel转化的淋巴细胞中,小干扰RNA介导的CAPERα敲低显著增强了软琼脂中的集落形成。由于Rel介导的反式激活能力是淋巴细胞转化的重要决定因素,Rel诱导转录抑制的能力也是如此,这些数据表明,CAPERα与Rel TAD的相互作用可能通过促进对肿瘤发生重要的特定基因子集的表达或抑制抑制来调节Rel/NF-κB的转化活性。总体而言,这项研究将CAPERα鉴定为v-Rel的一种新的转录共调节因子,并揭示了其在调节Rel致癌活性中的重要作用。