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紧密连接蛋白 ZO-2 调节转录因子 TEAD 的核积累。

Tight junction protein ZO-2 modulates the nuclear accumulation of transcription factor TEAD.

机构信息

Department of Physiology, Biophysics and Neuroscience, Mexico City 07360, Mexico.

Department of Toxicology, Center for Research and Advanced Studies (Cinvestav), Mexico City 07360, Mexico.

出版信息

Mol Biol Cell. 2021 Jul 15;32(15):1347-1358. doi: 10.1091/mbc.E20-07-0470. Epub 2021 May 19.

Abstract

The presence of tight junction protein onula ccludens 2 (ZO-2) at the nucleus inhibits the transcription of genes regulated by TEAD transcription factor. Here, we analyzed whether the movement of ZO-2 into the nucleus modulates the nuclear concentration of TEAD. In sparse cultures of ZO-2 knockdown Madin-Darby canine kidney cells, nuclear TEAD was diminished, as in parental cells transfected with a ZO-2 construct without nuclear localization signals, indicating that ZO-2 facilitates the entry of TEAD into the nucleus. Inhibition of nPKCδ in parental cells triggers the interaction between ZO-2 and TEAD at the cytoplasm and facilitates TEAD/ZO-2 complex nuclear importation. Using proximity ligation, immunoprecipitation, and pull-down assays, TEAD/ZO-2 interaction was confirmed. Nuclear TEAD is phosphorylated, and its exit in parental cells is enhanced by activation of a ZO-2 nuclear exportation signal by nPKCε, while the nuclear accumulation of ZO-2 triggered by the mutation of ZO-2 nuclear export signals induces no change in TEAD nuclear concentration. In summary, our results indicate that the movements of ZO-2 in and out of the nucleus modulate the intracellular traffic of TEAD through a process regulated by nPKCδ and ε and provide a novel role of ZO-2 as a nuclear translocator of TEAD.

摘要

紧密连接蛋白 zonula occludens 2(ZO-2)在核内的存在抑制了 TEAD 转录因子调节的基因的转录。在这里,我们分析了 ZO-2 进入核内是否调节了 TEAD 的核内浓度。在 ZO-2 敲低的 Madin-Darby 犬肾细胞稀疏培养物中,核内 TEAD 减少,这与没有核定位信号的 ZO-2 构建体转染的亲本细胞中的情况相同,表明 ZO-2 促进了 TEAD 进入核内。在亲本细胞中抑制 nPKCδ 会触发 ZO-2 和 TEAD 在细胞质中的相互作用,并促进 TEAD/ZO-2 复合物的核内导入。通过邻近连接、免疫沉淀和下拉测定证实了 TEAD/ZO-2 的相互作用。核内 TEAD 被磷酸化,并且 nPKCε 激活 ZO-2 的核输出信号会增强其在亲本细胞中的输出,而 ZO-2 核输出信号突变引发的 ZO-2 核内积累不会导致 TEAD 核内浓度发生变化。总之,我们的结果表明,ZO-2 在核内外的运动通过 nPKCδ 和 ε 调节的过程调节了 TEAD 的细胞内运输,并为 ZO-2 作为 TEAD 的核转位蛋白提供了新的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b55e/8694039/3aae4ea5bed1/mbc-32-1347-g001.jpg

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