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Transcription factories: genetic programming in three dimensions.

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TLDR
These studies apply innovative technical approaches to gain insights into the molecular constituents, dynamical behaviour and organizational regulators of transcription factories, providing exciting insightsinto the spatial dimension of transcriptional control.
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This article is published in Current Opinion in Genetics & Development.The article was published on 2012-04-01. It has received 132 citations till now. The article focuses on the topics: Transcription factories.

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Lamina-Associated Domains: Links with Chromosome Architecture, Heterochromatin, and Gene Repression

TL;DR: The properties of LADs, the molecular mechanisms that determine their association with the nuclear lamina, their dynamic links with other nuclear compartments, and their proposed roles in gene regulation are discussed.
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iRegulon: from a gene list to a gene regulatory network using large motif and track collections.

TL;DR: Over-activate p53 in breast cancer cells, followed by RNA-seq and ChIP-seq, and could identify an extensive up-regulated network controlled directly by p53 and a repressive network with no indication of direct p53 regulation but rather an indirect effect via E2F and NFY are mapped.
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The 3D Genome in Transcriptional Regulation and Pluripotency

TL;DR: The relationship between genome organization and lineage-specific transcriptional regulation is discussed in this paper, where the authors argue that the two are inextricably linked and that the relationship can be seen as a direct consequence of 3D genome organization.
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Global changes in the nuclear positioning of genes and intra- and interdomain genomic interactions that orchestrate B cell fate

TL;DR: A spectrum of genes that switched nuclear location during early B cell development was identified and these genes switched compartments to establish new intra- and interdomain interactions associated with a B lineage–specific transcription signature.
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Transcription factories: genome organization and gene regulation.

TL;DR: It is argued that transcription 'factories' are central organizers of the human genome during interphase, and that proximity to an appropriate factory determines the activity of a gene.
References
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Journal ArticleDOI

Capturing Chromosome Conformation

TL;DR: Using the yeast Saccharomyces cerevisiae, this work could confirm known qualitative features of chromosome organization within the nucleus and dynamic changes in that organization during meiosis and found that chromatin is highly flexible throughout.
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Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture–on-chip (4C)

TL;DR: It is demonstrated here that active and inactive genes are engaged in many long-range intrachromosomal interactions and can also form interchromosomal contacts and establish 4C technology as a powerful tool to study nuclear architecture.
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The multifunctional nucleolus

TL;DR: Although the nucleolus is primarily associated with ribosome biogenesis, several lines of evidence now show that it has additional functions, such as regulation of mitosis, cell-cycle progression and proliferation, many forms of stress response and biogenesis of multiple ribonucleoprotein particles.
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