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NRF2 和 p63 转录因子的相互作用促进表皮角质细胞的增殖。

Interaction of the NRF2 and p63 transcription factors promotes keratinocyte proliferation in the epidermis.

机构信息

Division of Cell Matrix Biology and Regenerative Medicine, FBMH, University of Manchester, M13 9PT, United Kingdom.

Department of Biology, Institute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.

出版信息

Nucleic Acids Res. 2021 Apr 19;49(7):3748-3763. doi: 10.1093/nar/gkab167.

Abstract

Epigenetic regulation of cell and tissue function requires the coordinated action of transcription factors. However, their combinatorial activities during regeneration remain largely unexplored. Here, we discover an unexpected interaction between the cytoprotective transcription factor NRF2 and p63- a key player in epithelial morphogenesis. Chromatin immunoprecipitation combined with sequencing and reporter assays identifies enhancers and promoters that are simultaneously activated by NRF2 and p63 in human keratinocytes. Modeling of p63 and NRF2 binding to nucleosomal DNA suggests their chromatin-assisted interaction. Pharmacological and genetic activation of NRF2 increases NRF2-p63 binding to enhancers and promotes keratinocyte proliferation, which involves the common NRF2-p63 target cyclin-dependent kinase 12. These results unravel a collaborative function of NRF2 and p63 in the control of epidermal renewal and suggest their combined activation as a strategy to promote repair of human skin and other stratified epithelia.

摘要

细胞和组织功能的表观遗传调控需要转录因子的协调作用。然而,它们在再生过程中的组合活性在很大程度上仍未被探索。在这里,我们发现了细胞保护转录因子 NRF2 和 p63 之间的一种意外相互作用,p63 是上皮形态发生的关键参与者。染色质免疫沉淀结合测序和报告基因分析鉴定了在人角质细胞中同时被 NRF2 和 p63 激活的增强子和启动子。p63 和 NRF2 与核小体 DNA 结合的建模表明它们具有染色质辅助的相互作用。NRF2 的药理学和遗传学激活增加了 NRF2-p63 对增强子的结合,并促进了角质细胞的增殖,这涉及到共同的 NRF2-p63 靶标细胞周期蛋白依赖性激酶 12。这些结果揭示了 NRF2 和 p63 在控制表皮更新中的协作功能,并表明它们的联合激活可以作为促进人类皮肤和其他分层上皮修复的一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f932/8053124/43c8ee4bd2b6/gkab167fig1.jpg

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