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Recruitment to the nuclear periphery can alter expression of genes in human cells.

TLDR
The data show that the radial position within the nucleus can influence the expression of some, but not all, genes, compatible with the suggestion that re-localisation of genes relative to the peripheral zone of the nucleus could be used by metazoans to modulate theexpression of selected genes during development and differentiation.
Abstract
The spatial organisation of the genome in the nucleus has a role in the regulation of gene expression. In vertebrates, chromosomal regions with low gene-density are located close to the nuclear periphery. Correlations have also been made between the transcriptional state of some genes and their location near the nuclear periphery. However, a crucial issue is whether this level of nuclear organisation directly affects gene function, rather than merely reflecting it. To directly investigate whether proximity to the nuclear periphery can influence gene expression in mammalian cells, here we relocate specific human chromosomes to the nuclear periphery by tethering them to a protein of the inner nuclear membrane. We show that this can reversibly suppress the expression of some endogenous human genes located near the tethering sites, and even genes further away. However, the expression of many other genes is not detectably reduced and we show that location at the nuclear periphery is not incompatible with active transcription. The dampening of gene expression around the nuclear periphery is dependent on the activity of histone deacetylases. Our data show that the radial position within the nucleus can influence the expression of some, but not all, genes. This is compatible with the suggestion that re-localisation of genes relative to the peripheral zone of the nucleus could be used by metazoans to modulate the expression of selected genes during development and differentiation.

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Citations
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Journal ArticleDOI

A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping

TL;DR: In situ Hi-C is used to probe the 3D architecture of genomes, constructing haploid and diploid maps of nine cell types, identifying ∼10,000 loops that frequently link promoters and enhancers, correlate with gene activation, and show conservation across cell types and species.
Journal ArticleDOI

Chromatin architecture reorganization during stem cell differentiation

TL;DR: Mapping genome-wide chromatin interactions in human embryonic stem cells and four human ES-cell-derived lineages reveals extensive chromatin reorganization during lineage specification, providing a global view of chromatin dynamics and a resource for studying long-range control of gene expression in distinct human cell lineages.
Journal ArticleDOI

Charting histone modifications and the functional organization of mammalian genomes

TL;DR: A selection of recent studies that have probed histone modifications and successive layers of chromatin structure in mammalian genomes, the patterns that have been identified and future directions for research are reviewed.
Journal ArticleDOI

Systematic Protein Location Mapping Reveals Five Principal Chromatin Types in Drosophila Cells

TL;DR: A repressive chromatin type is identified that covers about half of the genome and lacks classic heterochromatin markers and transcriptionally active euchromatin consists of two types that differ in molecular organization and H3K36 methylation and regulate distinct classes of genes.
Journal ArticleDOI

Molecular Maps of the Reorganization of Genome-Nuclear Lamina Interactions during Differentiation

TL;DR: High-resolution maps of genome-nuclear lamina interactions during subsequent differentiation of mouse embryonic stem cells via lineage-committed neural precursor cells into terminally differentiated astrocytes suggest that lamina-genome interactions are widely involved in the control of gene expression programs during lineage commitment and terminal differentiation.
References
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A new mathematical model for relative quantification in real-time RT-PCR.

TL;DR: This study enters into the particular topics of the relative quantification in real-time RT-PCR of a target gene transcript in comparison to a reference gene transcript and presents a new mathematical model that needs no calibration curve.
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Microarray data normalization and transformation

John Quackenbush
- 01 Dec 2002 - 
TL;DR: This review focuses on the much more mundane but indispensable tasks of 'normalizing' data from individual hybridizations to make meaningful comparisons of expression levels, and of 'transforming' them to select genes for further analysis and data mining.
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Self-renewal of pluripotent embryonic stem cells is mediated via activation of STAT3

TL;DR: Investigation of the role of STAT3 and inducible STAT3F in ES cells growing in the presence of LIF specifically abrogated self-renewal and promoted differentiation establish that STAT3 plays a central role in the maintenance of the pluripotential stem cell phenotype.
Journal ArticleDOI

Differences in the localization and morphology of chromosomes in the human nucleus

TL;DR: It is demonstrated that the distribution of genomic sequences between chromosomes has implications for nuclear structure and the findings are discussed in relation to a model of the human nucleus that is functionally compartmentalized.
Journal ArticleDOI

Three-Dimensional Maps of All Chromosomes in Human Male Fibroblast Nuclei and Prometaphase Rosettes

TL;DR: Modeling of 3D CT arrangements suggests that cell-type-specific differences in radial CT arrangements are not solely due to geometrical constraints that result from nuclear shape differences, and gene-density-correlated arrangements of higher-order chromatin shared by all human cell types studied so far are found.
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Trending Questions (1)
How does genomic location influence gene expression?

Genomic location can influence gene expression, with genes located near the nuclear periphery showing dampened expression in some cases.