Recruitment of polycomb group complexes and their role in the dynamic regulation of cell fate choice.

Development

Institut de Génétique Humaine, CNRS, 141 rue de la Cardonille, 34396 Montpellier Cedex 5, France.

Published: November 2009

Polycomb group (PcG) protein complexes dynamically define cellular identity through the regulation of key developmental genes. Important advances in the PcG field have come from genome-wide mapping studies in a variety of tissues and cell types that have analyzed PcG protein complexes, their associated histone marks and putative mechanisms of PcG protein recruitment. We review how these analyses have contributed to our understanding of PcG protein complex targeting to chromatin and consider the importance of diverse PcG protein complex composition for gene regulation. Finally, we focus on the dynamics of PcG protein complex action during cell fate transitions and on the implications of histone modifications for cell lineage commitment.

Download full-text PDF

Source
http://dx.doi.org/10.1242/dev.033902DOI Listing

Publication Analysis

Top Keywords

pcg protein
24
protein complex
12
polycomb group
8
cell fate
8
protein complexes
8
pcg
7
protein
6
recruitment polycomb
4
group complexes
4
complexes role
4

Similar Publications

Background: Glioblastoma (GBM) is the most common primary brain tumor in adults and has a median survival of less than 15 months. Advancements in the field of epigenetics have expanded our understanding of cancer biology and helped explain the molecular heterogeneity of these tumors. B-cell-specific Moloney murine leukemia virus insertion site-1 (Bmi-1) is a member of the highly conserved polycomb group (PcG) protein family that acts as a transcriptional repressor of multiple genes, including those that determine cell proliferation and differentiation.

View Article and Find Full Text PDF

Functional genomics of primary congenital glaucoma by pathway analysis and functional characterization of CYP1B1 mutations.

Vision Res

December 2024

Medical Biotechnology Laboratory, Dr. B. R. Ambedkar Center for Biomedical Research, University of Delhi, Delhi 110007, India. Electronic address:

CYP1B1 is the most common gene implicated in primary congenital glaucoma (PCG) - the most common form of childhood glaucoma. How CYP1B1 mutations cause PCG is not known. Understanding the mechanism of PCG caused by CYP1B1 mutations is crucial for disease management, therapeutics development, and potential prevention.

View Article and Find Full Text PDF

Evolutionary Nonindependence Between Human piRNAs and Their Potential Target Sites in Protein-Coding Genes.

J Mol Evol

December 2024

Bioinformatics Section, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China.

Article Synopsis
  • piRNAs are diverse small RNAs that help suppress transposable elements and are linked to protein-coding genes (PCGs) in the human genome.
  • This study utilized statistical analyses to show that there are nonrandom evolutionary forces influencing the relationships between piRNAs and their target PCGs, indicating a bias toward strengthening these connections.
  • Additionally, the research found that potential piRNA target sites are often located in Alu-derived regions of PCGs, highlighting the specific impact of these evolutionary forces on certain genomic areas.
View Article and Find Full Text PDF

Aim: Cerebral ischemic stroke (IS) is one of the leading causes of morbidity and mortality globally. However, the mechanisms underlying IS injury remain poorly understood. Ring finger protein 2 (RNF2), the member of the polycomb family (PcG), has been implicated in diverse biological and pathological conditions.

View Article and Find Full Text PDF

Polycomb protein RYBP facilitates super-enhancer activity.

Mol Med

November 2024

Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510080, China.

Background: Polycomb proteins are conventionally known as global repressors in cell fate determination. However, recent observations have shown their involvement in transcriptional activation, the mechanisms of which need further investigation.

Methods: Herein, multiple data from ChIP-seq, RNA-seq and HiChIP before or after RYBP depletion in embryonic stem cell (ESC), epidermal progenitor (EPC) and mesodermal cell (MEC) were analyzed.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!