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瞬时启动子相互作用调节发育基因激活。

Transient promoter interactions modulate developmental gene activation.

作者信息

Mahara Sylvia, Prüssing Sonja, Smialkovska Valeriia, Krall Samuel, Holliman Susannah, Blum Belinda, Dachtler Victoria, Borgers Helena, Sollier Etienne, Plass Christoph, Feldmann Angelika

机构信息

Mechanisms of Genome Control, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, Heidelberg, Germany.

Department of Biochemistry, University of Oxford, Oxford, UK.

出版信息

Mol Cell. 2024 Dec 5;84(23):4486-4502.e7. doi: 10.1016/j.molcel.2024.10.005. Epub 2024 Oct 29.

Abstract

Transcriptional induction coincides with the formation of various chromatin topologies. Strong evidence supports that gene activation is accompanied by a general increase in promoter-enhancer interactions. However, it remains unclear how these topological changes are coordinated across time and space during transcriptional activation. Here, we combine chromatin conformation capture with transcription and chromatin profiling during an embryonic stem cell (ESC) differentiation time course to determine how 3D genome restructuring is related to transcriptional transitions. This approach allows us to identify distinct topological alterations that are associated with the magnitude of transcriptional induction. We detect transiently formed interactions and demonstrate by genetic deletions that associated distal regulatory elements (DREs), as well as appropriate formation and disruption of these interactions, can contribute to the transcriptional induction of linked genes. Together, our study links topological dynamics to the magnitude of transcriptional induction and detects an uncharacterized type of transcriptionally important DREs.

摘要

转录诱导与各种染色质拓扑结构的形成同时发生。有力的证据支持基因激活伴随着启动子-增强子相互作用的普遍增加。然而,在转录激活过程中,这些拓扑变化如何在时间和空间上协调仍不清楚。在这里,我们在胚胎干细胞(ESC)分化时间进程中结合染色质构象捕获与转录和染色质分析,以确定三维基因组重组与转录转变之间的关系。这种方法使我们能够识别与转录诱导程度相关的不同拓扑改变。我们检测到瞬时形成的相互作用,并通过基因缺失证明相关的远端调控元件(DRE)以及这些相互作用的适当形成和破坏可有助于连锁基因的转录诱导。总之,我们的研究将拓扑动力学与转录诱导程度联系起来,并检测到一种未表征的转录重要DRE类型。

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