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NME1L对NF-κB信号传导调控中功能域的表征

Characterization of Functional Domains in NME1L Regulation of NF-κB Signaling.

作者信息

You Dong-Joo, Park Cho Rong, Mander Sunam, Ahn Curie, Seong Jae Young, Hwang Jong-Ik

机构信息

Graduate School of Medicine, Korea University, Seoul 136-705, Korea.

Transplantation Research Institute, Cancer Research Institute, Seoul National University, Seoul 110-799, Korea.

出版信息

Mol Cells. 2016 May 31;39(5):403-9. doi: 10.14348/molcells.2016.2320. Epub 2016 Apr 4.

Abstract

NME1 is a well-known metastasis suppressor which has been reported to be downregulated in some highly aggressive cancer cells. Although most studies have focused on NME1, the NME1 gene also encodes the protein (NME1L) containing N-terminal 25 extra amino acids by alternative splicing. According to previous studies, NME1L has potent anti-metastatic activity, in comparison with NME1, by interacting with IKKβ and regulating its activity. In the present study, we tried to define the role of the N-terminal 25 amino acids of NME1L in NF-κB activation signaling. Unfortunately, the sequence itself did not interact with IKKβ, suggesting that it may be not enough to constitute the functional structure. Further construction of NME1L fragments and biochemical analysis revealed that N-terminal 84 residues constitute minimal structure for homodimerization, IKKβ interaction and regulation of NF-κB signaling. The inhibitory effect of the fragment on cancer cell migration and NF-κB-stimulated gene expression was equivalent to that of whole NME1L. The data suggest that the N-terminal 84 residues may be a core region for the anti-metastatic activity of NME1L. Based on this result, further structural analysis of the binding between NME1L and IKKβ may help in understanding the anti-metastatic activity of NME1L and provide direction to NME1L and IKKβ-related anti-cancer drug design.

摘要

NME1是一种著名的转移抑制因子,据报道在一些高侵袭性癌细胞中表达下调。尽管大多数研究都集中在NME1上,但NME1基因也通过可变剪接编码一种含有N端额外25个氨基酸的蛋白质(NME1L)。根据以往的研究,与NME1相比,NME1L通过与IKKβ相互作用并调节其活性,具有强大的抗转移活性。在本研究中,我们试图确定NME1L的N端25个氨基酸在NF-κB激活信号通路中的作用。遗憾的是,该序列本身并不与IKKβ相互作用,这表明它可能不足以构成功能结构。进一步构建NME1L片段并进行生化分析发现,N端84个残基构成了同源二聚化、IKKβ相互作用和NF-κB信号调节的最小结构。该片段对癌细胞迁移和NF-κB刺激的基因表达的抑制作用与完整的NME1L相当。数据表明,N端84个残基可能是NME1L抗转移活性的核心区域。基于这一结果,进一步对NME1L与IKKβ之间的结合进行结构分析,可能有助于理解NME1L的抗转移活性,并为与NME1L和IKKβ相关的抗癌药物设计提供方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d5/4870188/792335d78f05/molce-39-5-403f1.jpg

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