Literature DB >> 17600113

Concise review: roles of polycomb group proteins in development and disease: a stem cell perspective.

Vinagolu K Rajasekhar1, Martin Begemann.   

Abstract

The acquisition and maintenance of cell fate are essential for metazoan growth and development. A strict coordination between genetic and epigenetic programs regulates cell fate determination and maintenance. Polycomb group (PcG) genes are identified as essential in these epigenetic developmental processes. These genes encode components of multimeric transcriptional repressor complexes that are crucial in maintaining cell fate. PcG proteins have also been shown to play a central role in stem cell maintenance and lineage specification. PcG proteins, together with a battery of components including sequence-specific DNA binding/accessory factors, chromatin remodeling factors, signaling pathway intermediates, noncoding small RNAs, and RNA interference machinery, generally define a dynamic cellular identity through tight regulation of specific gene expression patterns. Epigenetic modification of chromatin structure that results in expression silencing of specific genes is now emerging as an important molecular mechanism in this process. In embryonic stem (ES) cells and adult stem cells, such specific genes represent those associated with differentiation and development, and silencing of these genes in a PcG protein-dependent manner confers stemness. ES cells also contain novel chromatin motifs enriched in epigenetic modifications associated with both activation and repression of genes, suggesting that certain genes are poised for activation or repression. Interestingly, these chromatin domains are highly coincident with the promoters of developmental regulators, which are also found to be occupied by PcG proteins. The epigenetic integrity is compromised, however, by mutations or other alterations that affect the function of PcG proteins in stem cells leading to aberrant cell proliferation and tissue transformation, a hallmark of cancer. Disclosure of potential conflicts of interest is found at the end of this article.

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Year:  2007        PMID: 17600113     DOI: 10.1634/stemcells.2006-0608

Source DB:  PubMed          Journal:  Stem Cells        ISSN: 1066-5099            Impact factor:   6.277


  81 in total

1.  Nkx2.2 repressor complex regulates islet β-cell specification and prevents β-to-α-cell reprogramming.

Authors:  James B Papizan; Ruth A Singer; Shuen-Ing Tschen; Sangeeta Dhawan; Jessica M Friel; Susan B Hipkens; Mark A Magnuson; Anil Bhushan; Lori Sussel
Journal:  Genes Dev       Date:  2011-11-01       Impact factor: 11.361

2.  Definition of genetic events directing the development of distinct types of brain tumors from postnatal neural stem/progenitor cells.

Authors:  Falk Hertwig; Katharina Meyer; Sebastian Braun; Sara Ek; Rainer Spang; Cosima V Pfenninger; Isabella Artner; Gaëlle Prost; Xinbin Chen; Jaclyn A Biegel; Alexander R Judkins; Elisabet Englund; Ulrike A Nuber
Journal:  Cancer Res       Date:  2012-06-20       Impact factor: 12.701

Review 3.  Polycomb group proteins: multi-faceted regulators of somatic stem cells and cancer.

Authors:  Martin Sauvageau; Guy Sauvageau
Journal:  Cell Stem Cell       Date:  2010-09-03       Impact factor: 24.633

4.  MAPKAP kinase MK2 maintains self-renewal capacity of haematopoietic stem cells.

Authors:  Jessica Schwermann; Chozhavendan Rathinam; Maria Schubert; Stefanie Schumacher; Fatih Noyan; Haruhiko Koseki; Alexey Kotlyarov; Christoph Klein; Matthias Gaestel
Journal:  EMBO J       Date:  2009-04-16       Impact factor: 11.598

5.  Identification of methyllysine peptides binding to chromobox protein homolog 6 chromodomain in the human proteome.

Authors:  Nan Li; Richard S L Stein; Wei He; Elizabeth Komives; Wei Wang
Journal:  Mol Cell Proteomics       Date:  2013-07-10       Impact factor: 5.911

6.  Comparative analysis of chromatin binding by Sex Comb on Midleg (SCM) and other polycomb group repressors at a Drosophila Hox gene.

Authors:  Liangjun Wang; Neal Jahren; Ellen L Miller; Carrie S Ketel; Daniel R Mallin; Jeffrey A Simon
Journal:  Mol Cell Biol       Date:  2010-03-29       Impact factor: 4.272

7.  JDP2 (Jun Dimerization Protein 2)-deficient mouse embryonic fibroblasts are resistant to replicative senescence.

Authors:  Koji Nakade; Jianzhi Pan; Takahito Yamasaki; Takehide Murata; Bohdan Wasylyk; Kazunari K Yokoyama
Journal:  J Biol Chem       Date:  2009-02-20       Impact factor: 5.157

8.  EZH2-specific microRNA-98 inhibits human ovarian cancer stem cell proliferation via regulating the pRb-E2F pathway.

Authors:  Te Liu; Lengchen Hou; Yongyi Huang
Journal:  Tumour Biol       Date:  2014-04-27

9.  A misplaced lncRNA causes brachydactyly in humans.

Authors:  Philipp G Maass; Andreas Rump; Herbert Schulz; Sigmar Stricker; Lisanne Schulze; Konrad Platzer; Atakan Aydin; Sigrid Tinschert; Mary B Goldring; Friedrich C Luft; Sylvia Bähring
Journal:  J Clin Invest       Date:  2012-10-24       Impact factor: 14.808

10.  Nuclear receptor co-repressor is required to maintain proliferation of normal intestinal epithelial cells in culture and down-modulates the expression of pigment epithelium-derived factor.

Authors:  Geneviève Doyon; Stéphanie St-Jean; Mathieu Darsigny; Claude Asselin; Francois Boudreau
Journal:  J Biol Chem       Date:  2009-07-16       Impact factor: 5.157

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