核因子I家族成员是调控基因表达的关键转录因子。

IF 6.1 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Molecular & Cellular Proteomics Pub Date : 2025-01-01 Epub Date: 2024-11-29 DOI:10.1016/j.mcpro.2024.100890
Dicle Malaymar Pinar, Helka Göös, Zenglai Tan, Esa-Pekka Kumpula, Iftekhar Chowdhury, Zixian Wang, Qin Zhang, Kari Salokas, Salla Keskitalo, Gong-Hong Wei, Asli Kumbasar, Markku Varjosalo
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引用次数: 0

摘要

核因子I (NFI)转录因子家族(TFs)在细胞分化、增殖和稳态中起着关键作用。因此,NFI家族成员参与与其他蛋白质和染色质的大量相互作用。然而,尽管NFIs具有公认的重要性,但它们的相互作用、动态和功能尚未得到全面研究。在这里,我们采用互补的组学水平技术,即相互作用组学(亲和纯化质谱(AP-MS)和邻近依赖生物素化(BioID))和染色质免疫沉淀测序(ChIP-Seq),以获得NFI蛋白及其在不同细胞系中的相互作用的全面视图。我们的分析包括所有四个NFI家族成员,以及缺乏DNA结合域的NFIB短异构体(NFIB4)。我们观察到,尽管表现出冗余,但每个家族成员都有独特的高可信度相互作用基因和靶基因,这表明在转录调控网络中有不同的作用。研究表明,nfi与其他tf相互作用,共同调节广泛的调节网络和细胞过程。值得注意的是,时间依赖的接近性标记揭示了NFI蛋白-蛋白相互作用网络的高度动态性,并暗示了NFI相互作用的时间调节。此外,NFI相互作用组和靶组的基因本体(GO)富集分析揭示了NFI参与转录调控、染色质组织、细胞信号通路以及与癌症相关的途径。此外,我们观察到NFIB4与mRNA调控相关的蛋白质结合,这表明nfii的作用超出了传统的DNA结合和转录调节。鉴于nfi在调节其他tf的DNA结合能力及其与关键染色质重塑复合物的相互作用中所起的作用,因此我们提出nfi可能作为潜在的先驱tf发挥作用,从而影响广泛的细胞过程。这些对NFI蛋白-蛋白相互作用及其动态、上下文依赖性质的见解,提供了对基因调控机制的更深入理解,并暗示了NFI作为主要调节剂的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nuclear Factor I Family Members are Key Transcription Factors Regulating Gene Expression.

The Nuclear Factor I (NFI) family of transcription factors (TFs) plays key roles in cellular differentiation, proliferation, and homeostasis. As such, NFI family members engage in a large number of interactions with other proteins and chromatin. However, despite their well-established significance, the NFIs' interactomes, their dynamics, and their functions have not been comprehensively examined. Here, we employed complementary omics-level techniques, i.e. interactomics (affinity purification mass spectrometry (AP-MS) and proximity-dependent biotinylation (BioID)), and chromatin immunoprecipitation sequencing (ChIP-Seq), to obtain a comprehensive view of the NFI proteins and their interactions in different cell lines. Our analyses included all four NFI family members, and a less-studied short isoform of NFIB (NFIB4), which lacks the DNA binding domain. We observed that, despite exhibiting redundancy, each family member had unique high-confidence interactors and target genes, suggesting distinct roles within the transcriptional regulatory networks. The study revealed that NFIs interact with other TFs to co-regulate a broad range of regulatory networks and cellular processes. Notably, time-dependent proximity-labeling unveiled a highly dynamic nature of NFI protein-protein interaction networks and hinted at the temporal modulation of NFI interactions. Furthermore, gene ontology (GO) enrichment analysis of NFI interactome and targetome revealed the involvement of NFIs in transcriptional regulation, chromatin organization, cellular signaling pathways, and pathways related to cancer. Additionally, we observed that NFIB4 engages with proteins associated with mRNA regulation, which suggests that NFIs have roles beyond traditional DNA binding and transcriptional modulation. We propose that NFIs may function as potential pioneering TFs, given their role in regulating the DNA binding ability of other TFs and their interactions with key chromatin remodeling complexes, thereby influencing a wide range of cellular processes. These insights into NFI protein-protein interactions and their dynamic, context-dependent nature provide a deeper understanding of gene regulation mechanisms and hint at the role of NFIs as master regulators.

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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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