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Journal ArticleDOI

Transcriptional regulation by Polycomb group proteins.

TLDR
The current knowledge of the PRC complexes is discussed, how they are targeted to chromatin and how the high diversity of the PcG proteins allows these complexes to influence cell identity.
Abstract
Polycomb group (PcG) proteins function within Polycomb repressive complexes (PRCs), which modify histones and other proteins and silence target genes. This Review highlights new insights into the role of PcG proteins in gene regulation, specifically in controlling self-renewal and differentiation of embryonic stem cells, and into how PRCs are targeted to chromatin.

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Journal ArticleDOI

Chromatin repressive complexes in stem cells, development, and cancer.

TL;DR: The roles of the polycomb repressive complexes, PRC1 and PRC2, and the HDAC1- and HDAC2-containing complexes, NuRD, Sin3, and CoREST, in stem cells, development, and cancer, as well as the ongoing efforts to develop therapies targeting these complexes in human cancer are reviewed.
Journal ArticleDOI

Regulation of gene transcription by Polycomb proteins

TL;DR: The diversity of PcG complexes in mammalian cells is discussed, newly identified modes of recruitment to chromatin are examined, and the latest insights into the molecular mechanisms underlying the function of P cGs in transcription regulation and three-dimensional chromatin conformation are highlighted.
Journal ArticleDOI

Resetting Epigenetic Memory by Reprogramming of Histone Modifications in Mammals

TL;DR: Widespread resetting of epigenetic memory and striking plasticity of epigenome during gametogenesis and early development is revealed.
Journal ArticleDOI

The cancer epigenome: Concepts, challenges, and therapeutic opportunities

TL;DR: This review provides a broad context for recent developments that offer a greater understanding of how epigenetic regulators facilitate the initiation, maintenance, and evolution of cancer.
Journal ArticleDOI

Epigenetic control of CD8+ T cell differentiation.

TL;DR: The epigenetic processes that direct CD8+ T cell differentiation and function are reviewed, focusing on epigenetic modification of DNA and associated histones at genes and their regulatory elements and structural changes in chromatin organization that affect gene expression.
References
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Journal ArticleDOI

Crystal structure of the nucleosome core particle at 2.8 Å resolution

TL;DR: The X-ray crystal structure of the nucleosome core particle of chromatin shows in atomic detail how the histone protein octamer is assembled and how 146 base pairs of DNA are organized into a superhelix around it.
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High-resolution profiling of histone methylations in the human genome.

TL;DR: High-resolution maps for the genome-wide distribution of 20 histone lysine and arginine methylations as well as histone variant H2A.Z, RNA polymerase II, and the insulator binding protein CTCF across the human genome using the Solexa 1G sequencing technology are generated.
Journal ArticleDOI

Functional Demarcation of Active and Silent Chromatin Domains in Human HOX Loci by Noncoding RNAs

TL;DR: The transcriptional landscape of the four human HOX loci is characterized at five base pair resolution in 11 anatomic sites and 231 HOX ncRNAs are identified that extend known transcribed regions by more than 30 kilobases, suggesting transcription of ncRNA may demarcate chromosomal domains of gene silencing at a distance.
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A gene complex controlling segmentation in Drosophila.

TL;DR: The wild-type and mutant segmentation patterns are consistent with an antero-posterior gradient in repressor concentration along the embryo and a proximo-distal gradient along the chromosome in the affinities for repressor of each gene's cis-regulatory element.
Journal ArticleDOI

Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression

TL;DR: A model in which some lincRNAs guide chromatin-modifying complexes to specific genomic loci to regulate gene expression is proposed, and it is shown that siRNA-mediated depletion of certain linc RNAs associated with PRC2 leads to changes in gene expression.
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