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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

CBX2 Inhibits Neurite Development by Regulating Neuron-Specific Genes Expression

TL;DR: Evidence is provided that CBX2 is a negative regulator of neuronal differentiation, and it is found that the neuron-specific GAP-43 gene could contribute to the stimulating effect on neurite development associated with inhibition ofCBX2.
Journal ArticleDOI

Synovial sarcoma is a gateway to the role of chromatin remodeling in cancer

TL;DR: The key protein interactions of SS18-SSX that may qualify as primary targets for small molecule-based disruption leading to the development ofSS18- SSX-specific drugs may provide a specificity that ultimately improves survival while reducing morbidity of patients with synovial sarcoma.
Journal ArticleDOI

Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos.

TL;DR: It is found that ASXL3 protein knockdown during early embryo development highly perturbs neural cell fate specification, potentially resembling the Bainbridge-Ropers syndrome phenotype in humans.
Journal ArticleDOI

3D chromatin architecture and transcription regulation in cancer

TL;DR: In this paper , a review discusses key 3D chromatin structures (topologically associating domain, lamina-associated domain, and enhancer-promoter interactions) and corresponding structural protein elements mediating 3-dimensional chromatin interactions with a highlight of their associations with cancer.
Posted ContentDOI

Ki-67 Contributes To Normal Cell Cycle Progression And Inactive X Heterochromatin In p21 Checkpoint-Proficient Human Cells

TL;DR: It is demonstrated that depletion of Ki-67 in human hTERT-RPE1, WI-38, IMR90, h TERT-BJ cell lines and primary fibroblast cells slowed entry into S phase and coordinately downregulated genes related to DNA replication.
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.
Journal ArticleDOI

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.
Journal ArticleDOI

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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