衰老
生物
表观遗传学
染色质
细胞衰老
计算生物学
转录因子
基因表达
基因表达调控
转录组
基因
细胞生物学
遗传学
表型
作者
Song Qiao,Yuli Hou,Yiyin Zhang,Jing Liu,Yaqi Wang,Jingxuan Fu,Chi Zhang,Min Cao,Yuting Cui,Xiaomin Zhang,Xiaoling Wang,Jingjing Zhang,Congcong Liu,Yingzhen Zhang,Peichang Wang
摘要
Abstract Cellular senescence is a complex multifactorial biological phenomenon that plays essential roles in aging, and aging-related diseases. During this process, the senescent cells undergo gene expression altering and chromatin structure remodeling. However, studies on the epigenetic landscape of senescence using integrated multi-omics approaches are limited. In this research, we performed ATAC-seq, RNA-seq and ChIP-seq on different senescent types to reveal the landscape of senescence and identify the prime regulatory elements. We also obtained 34 key genes and deduced that NAT1, PBX1 and RRM2, which interacted with each other, could be the potential markers of aging and aging-related diseases. In summary, our work provides the landscape to study accessibility dynamics and transcriptional regulations in cellular senescence. The application of this technique in different types of senescence allows us to identify the regulatory elements responsible for the substantial regulation of transcription, providing the insights into molecular mechanisms of senescence.
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