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Open AccessJournal ArticleDOI

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

Material properties of phase-separated TFEB condensates regulate the autophagy-lysosome pathway

TL;DR: It is shown that liquid-like condensates of the transcription factor TFEB exhibit low fusion propensity in vitro and in living cells, and that the material properties of TFEBs can be harnessed to modulate T FEB activity.
Journal ArticleDOI

Live imaging of transcription sites using an elongating RNA polymerase II-specific probe.

TL;DR: In this paper, a modified Intacellular Antibilinear Antibody (mintbody) was used to detect the sites of RNAP2 Ser2ph-mintbody foci.
Journal ArticleDOI

Developmental disorders caused by haploinsufficiency of transcriptional regulators: a perspective based on cell fate determination

Roman Zug
- 15 Jan 2022 - 
TL;DR: In this article , the authors propose the hypothesis that developmental disorders are caused by defects in cell fate determination that are based on disrupted bistability in the underlying gene regulatory network (GRN), a crucial system biology concept to model binary choices such as cell fate decisions, requires both positive feedback and ultrasensitivity, the latter often achieved through TF cooperativity.
Posted ContentDOI

Mechanistic inferences from analysis of measurements of protein phase transitions in live cells

TL;DR: This work reports the development of a supervised method to obtain automated and accurate classifications of phase transitions quantified using the DAmFRET assay, and uncovers well-established and surprising new sequence features that contribute to two-state phase behavior of prion-like domains.
Posted Content

Action at a distance in transcriptional regulation

TL;DR: A minimal model is explored that embodies the idea that droplet-mediated interactions can account for crucial features of gene regulation only if the droplet is poised at a non-generic point in its phase diagram.
References
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Journal ArticleDOI

Fiji: an open-source platform for biological-image analysis

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.
Journal ArticleDOI

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.
Journal ArticleDOI

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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