Dipartimento di Scienze della Vita, Università degli Studi di Modena e Reggio Emilia, Via Campi 213/D, 41125 Modena, Italy.
Centro Interdipartimentale Grandi Strumenti, Università degli Studi di Modena e Reggio Emilia, Via Campi 213/A, 41125 Modena, Italy.
Biochim Biophys Acta Gene Regul Mech. 2018 May;1861(5):509-518. doi: 10.1016/j.bbagrm.2018.02.008. Epub 2018 Mar 2.
The heterotrimeric NF-Y complex is a pioneer factor that binds to CCAAT-genes and regulates their transcription. NF-Y cooperates with multiple transcription factors and co-regulators in order to positively or negatively influence gene transcription. The recruitment of NF-Y to CCAAT box is significantly enriched in cancer-associated gene promoters loci and positively correlates with malignancy. NF-Y subunits, in particular the DNA-binding subunit NF-YA and the histone-fold subunit NF-YC, appear overexpressed in specific types of cancer. Here we demonstrate that NF-Y subunits expression is finely regulated through transcriptional and post-translational mechanisms thus allowing control over basal expression levels. NF-Y negatively regulates the transcription of the genes encoding for its subunits. DNA pull-down/affinity purification assay coupled with Mass Spectrometry identified putative co-regulators, such as Lamin A, involved in NF-YA gene transcription level. We also evidentiate how the stability of the complex is severely affected by the absence of one subunit. Our results identified for the first time one of the mechanisms responsible for NF-Y expression, which may be involved in the aberrant expression and activity observed in tumor cells and other pathological conditions.
异三聚体 NF-Y 复合物是一种先驱因子,它与 CCAAT-基因结合并调节其转录。NF-Y 与多个转录因子和共调节因子合作,以正向或负向影响基因转录。NF-Y 被招募到 CCAAT 盒的情况在与癌症相关的基因启动子位点中显著富集,并与恶性程度呈正相关。NF-Y 亚基,特别是 DNA 结合亚基 NF-YA 和组蛋白折叠亚基 NF-YC,在特定类型的癌症中过度表达。在这里,我们证明 NF-Y 亚基的表达通过转录和翻译后机制进行精细调节,从而可以控制基础表达水平。NF-Y 负调节其亚基基因的转录。DNA 下拉/亲和纯化测定与质谱联用鉴定了参与 NF-YA 基因转录水平的潜在共调节因子,如核纤层蛋白 A。我们还证明了复合物的稳定性如何因一个亚基的缺失而受到严重影响。我们的结果首次确定了 NF-Y 表达的一种机制,该机制可能与肿瘤细胞和其他病理情况下观察到的异常表达和活性有关。