ChIP-Seq data from IMR90 Control and IMR90 HRAS-G12V using an H3K79me3 antibody
收藏干细胞与再生医学数据中心2022-02-20 更新2024-03-06 收录
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Oncogene-induced senescent cells display a robust change in their epigenome and have increased transcription and secretion of numerous pro-inflammatory cytokines and chemokines termed the senescence-associated secretory phenotype (SASP). Therefore, understanding how and if the epigenome is involved in regulating the transcription of the SASP is critical to understanding how to restrain the harmful effects of the SASP. The active histone marks H3K79me2 and H3K79me3 and their methyltransferase DOT1L are increased during oncogene-induced senescence. Whether H3K79 methylation and DOT1L expression are involved in the transcriptional regulation of the SASP is unknown.
提供机构：
Penn State College of MEdicine
创建时间：
2022-02-20
