Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan, USA.
Immunology. 2022 Sep;167(1):105-121. doi: 10.1111/imm.13527. Epub 2022 Jul 7.
Cells must control genes that are induced by virus infection to mitigate deleterious consequences of inflammation. We investigated the mechanisms whereby Keap1 moderates the transcription of genes that are induced by Sendai virus infection in mouse embryo fibroblasts (MEFs). Keap1-/- deletions increased the transcription of virus induced genes independently of Nrf2. Keap1 moderated early virus induced gene transcription. Virus infection induced Keap1 to bind Ifnb1, Tnf and Il6, and reduced Keap1 binding at Cdkn1a and Ccng1. Virus infection induced G9a-GLP and NFκB p50 recruitment, and H3K9me2 deposition. Keap1-/- deletions eliminated G9a-GLP and NFκB p50 recruitment, and H3K9me2 deposition, but they did not affect NFκB p65, IRF3 or cJun recruitment. G9a-GLP inhibitors (BIX01294, MS012, BRD4770) enhanced virus induced gene transcription in MEFs with intact Keap1, but not in MEFs with Keap1-/- deletions. G9a-GLP inhibitors augmented Keap1 binding to virus induced genes in infected MEFs, and to cell cycle genes in uninfected MEFs. G9a-GLP inhibitors augmented NFκB subunit recruitment in MEFs with intact Keap1. G9a-GLP inhibitors stabilized Keap1 retention in permeabilized MEFs. G9a-GLP lysine methyltransferase activity was required for Keap1 to moderate transcription, and it moderated Keap1 binding to chromatin. The interdependent effects of Keap1 and G9a-GLP on the recruitment of each other and on the moderation of virus induced gene transcription constitute a feedback circuit. Keap1 and the electrophile tBHQ reduced virus induced gene transcription through different mechanisms, and they regulated the recruitment of different NFκB subunits. Characterization of the mechanisms whereby Keap1, G9a-GLP and NFκB p50 moderate virus induced gene transcription can facilitate the development of immunomodulatory agents.
细胞必须控制受病毒感染诱导的基因,以减轻炎症的有害后果。我们研究了 Keap1 调节小鼠胚胎成纤维细胞 (MEFs) 中受仙台病毒感染诱导的基因转录的机制。Keap1-/-缺失独立于 Nrf2 增加了病毒诱导基因的转录。Keap1 调节早期病毒诱导基因的转录。病毒感染诱导 Keap1 结合 Ifnb1、Tnf 和 Il6,并减少 Keap1 在 Cdkn1a 和 Ccng1 上的结合。病毒感染诱导 G9a-GLP 和 NFκB p50 的募集,并导致 H3K9me2 沉积。Keap1-/-缺失消除了 G9a-GLP 和 NFκB p50 的募集以及 H3K9me2 的沉积,但不影响 NFκB p65、IRF3 或 cJun 的募集。G9a-GLP 抑制剂 (BIX01294、MS012、BRD4770) 增强了具有完整 Keap1 的 MEFs 中病毒诱导基因的转录,但在 Keap1-/-缺失的 MEFs 中没有作用。G9a-GLP 抑制剂增强了感染 MEFs 中病毒诱导基因以及未感染 MEFs 中细胞周期基因上 Keap1 的结合。G9a-GLP 抑制剂增强了具有完整 Keap1 的 MEFs 中 NFκB 亚基的募集。G9a-GLP 抑制剂稳定了透化 MEFs 中 Keap1 的保留。G9a-GLP 赖氨酸甲基转移酶活性是 Keap1 调节转录所必需的,它调节 Keap1 与染色质的结合。Keap1 和 G9a-GLP 对彼此募集和调节病毒诱导基因转录的相互依赖的影响构成了一个反馈回路。Keap1 和亲电试剂 tBHQ 通过不同的机制降低病毒诱导基因的转录,并调节不同的 NFκB 亚基的募集。阐明 Keap1、G9a-GLP 和 NFκB p50 调节病毒诱导基因转录的机制可以促进免疫调节剂的开发。