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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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Why are so many MLL lysine methyltransferases required for normal mammalian development

TL;DR: The mixed lineage leukemia (MLL) family of proteins became known initially for the leukemia link of its founding member, but over the decades has been recognized as an important class of histone H3 lysine 4 (H3K4) methyltransferases that control key aspects of normal cell physiology and development.
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Nascent RNA scaffolds contribute to chromosome territory architecture and counter chromatin compaction.

TL;DR: In this paper, the authors investigate whether non-coding RNA broadly contributes to cytological-scale chromosome territory architecture, and they find that most RNA in the nuclear scaffold is repeat-rich, noncoding, and derived predominantly from introns of nascent transcripts.
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Tracking and interpreting long-range chromatin interactions with super-resolution live-cell imaging.

TL;DR: How 3D super-resolution live-cell imaging (SRLCI) can resolve open questions on the dynamic formation and dissolution of chromatin interactions is discussed and SRLCI approaches will likely emerge as a critical tool to dynamically probe 3D genome structure and function and to study enhancer-promoter interactions and chromatin looping.
Journal ArticleDOI

Transcription factors: building hubs in the 3D space.

TL;DR: The nature, organizational principles, and potential function of complex topological assemblies, including the recently reported enhancer “hubs,” “cliques,’ and FIREs (frequently interacting regions) as well as multi-contact hubs are discussed.
Journal ArticleDOI

From start to end: Phase separation and transcriptional regulation.

TL;DR: This review summarizes the process of phase separation involved in heterochromatin formation and chromatin remodeling, transcriptional regulation and post-transcriptional regulation, and provides a reference for understanding gene regulation during cell identity and disease development.
References
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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.
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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.
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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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