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计算鉴定乳腺癌细胞中 ERRα 的新潜在转录伙伴:特定靶标对应特定伙伴。

Computational identification of new potential transcriptional partners of ERRα in breast cancer cells: specific partners for specific targets.

机构信息

Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon 1, CNRS UMR5242, Ecole Normale Supérieure de Lyon, 32-34 Avenue Tony Garnier, 69007, Lyon, France.

The Center for Bioinformatics and Computational Biology, Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai, China.

出版信息

Sci Rep. 2022 Mar 9;12(1):3826. doi: 10.1038/s41598-022-07744-w.

Abstract

Estrogen related receptors are orphan members of the nuclear receptor superfamily acting as transcription factors (TFs). In contrast to classical nuclear receptors, the activities of the ERRs are not controlled by a natural ligand. Regulation of their activities thus relies on availability of transcriptional co-regulators. In this paper, we focus on ERRα, whose involvement in cancer progression has been broadly demonstrated. We propose a new approach to identify potential co-activators, starting from previously identified ERRα-activated genes in a breast cancer (BC) cell line. Considering mRNA gene expression from two sets of human BC cells as major endpoint, we used sparse partial least squares modeling to uncover new transcriptional regulators associated with ERRα. Among them, DDX21, MYBBP1A, NFKB1, and SETD7 are functionally relevant in MDA-MB-231 cells, specifically activating the expression of subsets of ERRα-activated genes. We studied SET7 in more details and showed its co-localization with ERRα and its ERRα-dependent transcriptional and phenotypic effects. Our results thus demonstrate the ability of a modeling approach to identify new transcriptional partners from gene expression. Finally, experimental results show that ERRα cooperates with distinct co-regulators to control the expression of distinct sets of target genes, thus reinforcing the combinatorial specificity of transcription.

摘要

雌激素相关受体是核受体超家族的孤儿成员,作为转录因子 (TF) 发挥作用。与经典核受体不同,ERR 的活性不受天然配体的控制。因此,它们的活性调节依赖于转录共调节剂的可用性。在本文中,我们专注于 ERRα,其在癌症进展中的作用已得到广泛证明。我们提出了一种新的方法来识别潜在的共激活剂,从乳腺癌 (BC) 细胞系中先前鉴定的 ERRα 激活基因开始。考虑到两组人类 BC 细胞的 mRNA 基因表达作为主要终点,我们使用稀疏偏最小二乘建模来揭示与 ERRα 相关的新转录调节剂。其中,DDX21、MYBBP1A、NFKB1 和 SETD7 在 MDA-MB-231 细胞中具有功能相关性,特别激活了 ERRα 激活基因的亚群表达。我们更详细地研究了 SET7,并显示其与 ERRα 共定位及其 ERRα 依赖性转录和表型效应。因此,我们的研究结果证明了建模方法从基因表达中识别新转录伙伴的能力。最后,实验结果表明,ERRα 与不同的共调节因子合作来控制不同靶基因的表达,从而增强了转录的组合特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39eb/8907200/dffefd51ba15/41598_2022_7744_Fig1_HTML.jpg

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