Milavetz Barry, Dawlaty Ranna, Haugen Jacob
Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, 58202, USA.
Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, 58202, USA.
Tumour Virus Res. 2025 Jul 31;20:200326. doi: 10.1016/j.tvr.2025.200326.
Since early and late transcription are both regulated from the same central regulatory region in SV40 chromatin, the location of nucleosomes carrying histone modifications may contribute to controlling the direction of transcription from the regulatory region. This could occur through the generation of active chromatin in the direction of transcription and repressive chromatin in the opposite direction. In order to test this hypothesis, we have characterized the products of SV40 transcription and location of nucleosomes carrying histone modifications in SV40 chromatin following treatment of infected cells with inhibitors of histone methylation metabolism. The inhibitors used included GSK-LSD1 to inhibit demethylation of H3K4me1 and H3K9me1, A366 to inhibit the introduction of H3K9me1, and UNC1999 to inhibit the introduction of H3K27me3. The results are consistent with a regulatory model in which nucleosomes carrying H3K9me1 and H3K27me3 located at the ends of the SV40 regulatory region act to regulate transcription.
由于SV40染色质的早期和晚期转录均受同一中央调控区域调控,携带组蛋白修饰的核小体的位置可能有助于控制调控区域的转录方向。这可能是通过在转录方向上产生活性染色质,而在相反方向上产生抑制性染色质来实现的。为了验证这一假设,我们在用组蛋白甲基化代谢抑制剂处理感染细胞后,对SV40转录产物以及SV40染色质中携带组蛋白修饰的核小体的位置进行了表征。所使用的抑制剂包括抑制H3K4me1和H3K9me1去甲基化的GSK-LSD1、抑制H3K9me1引入的A366以及抑制H3K27me3引入的UNC1999。结果与一个调控模型一致,即位于SV40调控区域末端携带H3K9me1和H3K27me3的核小体起到调控转录的作用。