Department of Medical Physiology, Kyorin University School of Medicine, Tokyo 181-8611, Japan.
Department of Pharmacology and Toxicology, Kyorin University School of Medicine, Tokyo 181-8611, Japan.
Biomolecules. 2021 Jan 23;11(2):146. doi: 10.3390/biom11020146.
The HPC-1/syntaxin 1A () gene, which is involved in synaptic transmission and neurodevelopmental disorders, is a TATA-less gene with several transcription start sites. It is activated by the binding of Sp1 and acetylated histone H3 to the -204 to +2 core promoter region (CPR) in neuronal cell/tissue. Furthermore, it is depressed by the association of class 1 histone deacetylases (HDACs) to -CPR in non-neuronal cell/tissue. To further clarify the factors characterizing gene silencing in non-neuronal cell/tissue not expressing , we attempted to identify the promoter region forming DNA-protein complex only in non-neuronal cells. Electrophoresis mobility shift assays (EMSA) demonstrated that the -183 to -137 OL2 promoter region forms DNA-protein complex only in non-neuronal fetal rat skin keratinocyte (FRSK) cells which do not express . Furthermore, the Yin-Yang 1 (YY1) transcription factor binds to the -183 to -137 promoter region of in FRSK cells, as shown by competitive EMSA and supershift assay. Chromatin immunoprecipitation assay revealed that YY1 in vivo associates to -CPR in cell/tissue not expressing and that trichostatin A treatment in FRSK cells decreases the high-level association of YY1 to -CPR in default. Reporter assay indicated that YY1 negatively regulates transcription. Finally, mass spectrometry analysis showed that gene silencing factors, including HDAC1, associate onto the -183 to -137 promoter region together with YY1. The current study is the first to report that transcription is negatively regulated in a cell/tissue-specific manner by YY1 transcription factor, which binds to the -183 to -137 promoter region together with gene silencing factors, including HDAC.
HPC-1/syntaxin 1A()基因参与突触传递和神经发育障碍,是一个缺乏 TATA 框的基因,有多个转录起始位点。它在神经元细胞/组织中通过 Sp1 和乙酰化组蛋白 H3 与-204 到+2 核心启动子区域(CPR)的结合而被激活。此外,它在非神经元细胞/组织中通过与 -CPR 结合的 I 类组蛋白去乙酰化酶(HDACs)的关联而被抑制。为了进一步阐明在不表达的非神经元细胞/组织中特征化基因沉默的因素,我们试图鉴定仅在非神经元细胞中形成 DNA-蛋白复合物的启动子区域。电泳迁移率变动分析(EMSA)表明,-183 到-137 OL2 启动子区域仅在不表达的非神经元胎鼠皮肤角质形成细胞(FRSK)中形成 DNA-蛋白复合物。此外,正如竞争 EMSA 和超迁移实验所示,阴阳 1(YY1)转录因子与 FRSK 细胞中的 结合。染色质免疫沉淀实验表明,YY1 在体内与不表达的细胞/组织中的 -CPR 结合,并且 Trichostatin A 在 FRSK 细胞中的处理降低了 YY1 对默认情况下 -CPR 的高水平结合。报告基因实验表明,YY1 负调控的转录。最后,质谱分析表明,包括 HDAC1 在内的基因沉默因子与 YY1 一起结合到-183 到-137 启动子区域。本研究首次报道,YY1 转录因子以细胞/组织特异性方式负调控转录,该转录因子与包括 HDAC 在内的基因沉默因子一起结合到-183 到-137 启动子区域。