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利用蛋白质结合微阵列(PBM)表征核因子κB(NF-κB)的DNA结合位点特异性。

Characterizing the DNA binding site specificity of NF-κB with protein-binding microarrays (PBMs).

作者信息

Siggers Trevor, Gilmore Thomas D, Barron Brian, Penvose Ashley

机构信息

Department of Biology, Boston University, 5 Cummington Mall, Boston, MA, 02215, USA,

出版信息

Methods Mol Biol. 2015;1280:609-30. doi: 10.1007/978-1-4939-2422-6_36.

Abstract

NF-κB transcription factors control a wide array of important cellular and organismal processes in eukaryotes. All NF-κB transcription factors bind to DNA target sites as dimers. In vertebrates, there are five NF-κB subunits, p50, p52, RelA (p65), c-Rel, and RelB, that can form almost all combinations of homodimers and heterodimers, which recognize distinct, but overlapping, target sequences. In this chapter, we describe the use of protein-binding microarrays (PBMs), a high-throughput method to measure the binding of proteins to different DNA sequences. PBM datasets allow for sensitive comparisons of NF-κB dimer DNA-binding differences and can aid in the computational and experimental prediction of NF-κB target genes.

摘要

核因子κB(NF-κB)转录因子控制着真核生物中一系列重要的细胞和机体过程。所有NF-κB转录因子均以二聚体形式与DNA靶位点结合。在脊椎动物中,有五个NF-κB亚基,即p50、p52、RelA(p65)、c-Rel和RelB,它们可以形成几乎所有同型二聚体和异型二聚体的组合,这些二聚体识别不同但有重叠的靶序列。在本章中,我们描述了蛋白质结合微阵列(PBM)的使用,这是一种用于测量蛋白质与不同DNA序列结合的高通量方法。PBM数据集能够对NF-κB二聚体的DNA结合差异进行灵敏比较,并有助于对NF-κB靶基因进行计算和实验预测。

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