Dysregulation of histone methylation in SV40 chromosomes during replication results in aberrant transcription and chromatin structure.

IF 8.1 Q1 VIROLOGY
Barry Milavetz, Ranna Dawlaty, Jacob Haugen
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引用次数: 0

Abstract

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.

SV40染色体在复制过程中组蛋白甲基化失调导致转录和染色质结构异常。
由于SV40染色质的早期和晚期转录都受到同一个中央调控区域的调控,因此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。这可以通过在转录方向上产生活性染色质和在相反方向上产生抑制染色质来发生。为了验证这一假设,我们在用组蛋白甲基化代谢抑制剂治疗感染细胞后,表征了SV40转录产物和SV40染色质中携带组蛋白修饰的核小体的位置。使用的抑制剂包括GSK-LSD1抑制H3K4me1和H3K9me1的去甲基化,A366抑制H3K9me1的引入,UNC1999抑制H3K27me3的引入。该结果与位于SV40调控区末端携带H3K9me1和H3K27me3的核小体调节转录的调控模型一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tumour Virus Research
Tumour Virus Research Medicine-Infectious Diseases
CiteScore
6.50
自引率
2.30%
发文量
16
审稿时长
56 days
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