Stilo Romania, Varricchio Ettore, Liguoro Domenico, Leonardi Antonio, Vito Pasquale
Dip. Scienze Biologiche ed Ambientali, Università degli Studi del Sannio di Benevento, Via Port'Arsa 11, 82100 Benevento, Italy.
J Cell Sci. 2008 Apr 15;121(Pt 8):1165-71. doi: 10.1242/jcs.021105. Epub 2008 Mar 18.
The molecular complex containing CARMA proteins, BCL10 and TRAF6 has been identified recently as a key component in the signal transduction pathways that regulate activation of the nuclear factor kappaB (NF-kappaB) transcription factor. Here, we report that the inducible protein A20 negatively regulates these signaling cascades by means of its deubiquitylation activity. We show that A20 perturbs assembly of the complex containing CARMA3, BCL10 and IKKgamma/NEMO, thereby suppressing activation of NF-kappaB. Together, our results further define the molecular mechanisms that control activation of NF-kappaB and reveal a function for A20 in the regulation of CARMA and BCL10 activity in lymphoid and non-lymphoid cells.
最近,包含CARMA蛋白、BCL10和TRAF6的分子复合物已被确定为调节核因子κB(NF-κB)转录因子激活的信号转导途径中的关键成分。在此,我们报告诱导性蛋白A20通过其去泛素化活性对这些信号级联反应进行负调控。我们表明,A20干扰了包含CARMA3、BCL10和IKKγ/NEMO的复合物的组装,从而抑制了NF-κB的激活。总之,我们的结果进一步明确了控制NF-κB激活的分子机制,并揭示了A20在调节淋巴细胞和非淋巴细胞中CARMA和BCL10活性方面的功能。