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Mediator and RNA polymerase II clusters associate in transcription-dependent condensates

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TLDR
This work used live-cell superresolution and light-sheet imaging to study the organization and dynamics of the Mediator coactivator and RNA polymerase II (Pol II) directly and suggests that large clusters of Mediator, recruited by transcription factors at large or clustered enhancer elements, interact with large Pol II clusters in transcriptional condensates in vivo.
Abstract
Models of gene control have emerged from genetic and biochemical studies, with limited consideration of the spatial organization and dynamics of key components in living cells. We used live-cell superresolution and light-sheet imaging to study the organization and dynamics of the Mediator coactivator and RNA polymerase II (Pol II) directly. Mediator and Pol II each form small transient and large stable clusters in living embryonic stem cells. Mediator and Pol II are colocalized in the stable clusters, which associate with chromatin, have properties of phase-separated condensates, and are sensitive to transcriptional inhibitors. We suggest that large clusters of Mediator, recruited by transcription factors at large or clustered enhancer elements, interact with large Pol II clusters in transcriptional condensates in vivo.

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Journal ArticleDOI

Dynamics of transcriptional enhancers and chromosome topology in gene regulation

TL;DR: It is proposed that assembly of “transcription hubs” in the context of 3D genome structure plays an important role in transcriptional regulation.
Posted Content

Bridging-induced microphase separation: photobleaching experiments, chromatin domains, and the need for active reactions

TL;DR: The mechanism and consequences of the 'bridging-induced attraction' are reviewed, a generic biophysical principle that underpins some existing models for chromosome organization in 3D and provides an explanation for the biogenesis of nuclear bodies and transcription factories via microphase separation.
Journal ArticleDOI

Liquid demixing in elastic networks: Cavitation, permeation, or size selection?

- 01 Mar 2022 - 
TL;DR: In this article , the trade-offs between elastic, wetting, and interfacial energies of phase-separated liquid condensates interact mechanically with surrounding elastic networks such as chromatin and cytoskeleton.
References
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TL;DR: Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis that facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system.
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Imaging intracellular fluorescent proteins at nanometer resolution.

TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
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Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

TL;DR: A high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores that can, in principle, reach molecular-scale resolution is developed.
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Selective inhibition of BET bromodomains.

TL;DR: A cell-permeable small molecule (JQ1) that binds competitively to acetyl-lysine recognition motifs, or bromodomains is reported, establishing proof-of-concept for targeting protein–protein interactions of epigenetic ‘readers’, and providing a versatile chemical scaffold for the development of chemical probes more broadly throughout the b romodomain family.
Journal ArticleDOI

Ultra-High Resolution Imaging by Fluorescence Photoactivation Localization Microscopy

TL;DR: A new method for fluorescence imaging has been developed that can obtain spatial distributions of large numbers of fluorescent molecules on length scales shorter than the classical diffraction limit, and suggests a means to address a significant number of biological questions that had previously been limited by microscope resolution.
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