Toledano M B, Ghosh D, Trinh F, Leonard W J
Section on Pulmonary and Molecular Immunology, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892.
Mol Cell Biol. 1993 Feb;13(2):852-60. doi: 10.1128/mcb.13.2.852-860.1993.
We previously reported that either oxidation or alkylation of NF-kappa B in vitro abrogates DNA binding. We used this phenomenon to help elucidate structural determinants of NF-kappa B binding. We now demonstrate that Cys-62 of NF-kappa B p50 mediates the redox effect and lies within an N-terminal region required for DNA binding but not for dimerization. Several point mutations in this region confer a transdominant negative binding phenotype to p50. The region is highly conserved in all Rel family proteins, and we have determined that it is also critical for DNA binding of NF-kappa B p65. Replacement of the N-terminal region of p65 with the corresponding region from p50 changes its DNA-binding specificity towards that of p50. These data suggest that the N-terminal regions of p50 and p65 are critical for DNA binding and help determine the DNA-binding specificities of p50 and p65. We have defined within the N-terminal region a sequence motif, R(F/G)(R/K)YXCE, which is present in Rel family proteins and also in zinc finger proteins capable of binding to kappa B sites. The potential significance of this finding is discussed.
我们之前报道过,在体外对核因子-κB(NF-κB)进行氧化或烷基化处理会消除其与DNA的结合。我们利用这一现象来帮助阐明NF-κB结合的结构决定因素。我们现在证明,NF-κB p50的半胱氨酸-62介导了氧化还原效应,且位于DNA结合所需的N端区域内,但并非二聚化所需区域。该区域的几个点突变赋予了p50显性负性结合表型。该区域在所有Rel家族蛋白中高度保守,并且我们已经确定它对NF-κB p65的DNA结合也至关重要。用p50的相应区域替换p65的N端区域会使其DNA结合特异性变为p50的DNA结合特异性。这些数据表明,p50和p65的N端区域对DNA结合至关重要,并有助于确定p50和p65的DNA结合特异性。我们在N端区域内定义了一个序列基序,即R(F/G)(R/K)YXCE,它存在于Rel家族蛋白以及能够结合κB位点的锌指蛋白中。本文讨论了这一发现的潜在意义。