Literature DB >> 16914306

Polycomb response elements and targeting of Polycomb group proteins in Drosophila.

Jürg Müller1, Judith A Kassis.   

Abstract

Polycomb group (PcG) proteins are conserved regulatory proteins that repress transcription of particular target genes in animals and plants. Studies over the past decade have established that most PcG proteins are not classic DNA binding factors but that they exist in multisubunit protein complexes that bind to and modify chromatin. Nevertheless, PcG repression of target genes in Drosophila requires specific cis-regulatory sequences, called Polycomb response elements (PREs), and chromatin immunoprecipitation studies have shown that, in vivo, most PcG proteins are specifically bound at the PREs of target genes. However, the mechanisms by which these PcG protein complexes are recruited to PREs and how they repress transcription are still poorly understood. Recent studies challenge earlier models that invoke covalent histone modifications and chromatin binding as the key steps in the recruitment of PcG proteins to PREs. The available evidence suggests that PREs are largely devoid of nucleosomes and that PRE DNA serves as an assembly platform for many different PcG protein complexes through DNA-protein and protein-protein interactions. The emerging picture suggests that the binding and modification of chromatin by PcG proteins is needed for interaction of PRE-tethered PcG protein complexes with nucleosomes in the flanking chromatin in order to maintain a Polycomb-repressed chromatin state at promoters and coding regions of target genes.

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Year:  2006        PMID: 16914306     DOI: 10.1016/j.gde.2006.08.005

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  129 in total

1.  The homeodomain protein hmbx-1 maintains asymmetric gene expression in adult C. elegans olfactory neurons.

Authors:  Bluma J Lesch; Cornelia I Bargmann
Journal:  Genes Dev       Date:  2010-08-15       Impact factor: 11.361

2.  Recruitment of polycomb complexes: a role for SCM.

Authors:  Judith A Kassis; James A Kennison
Journal:  Mol Cell Biol       Date:  2010-03-29       Impact factor: 4.272

3.  Wapl antagonizes cohesin binding and promotes Polycomb-group silencing in Drosophila.

Authors:  Melissa D Cunningham; Maria Gause; Yuzhong Cheng; Amanda Noyes; Dale Dorsett; James A Kennison; Judith A Kassis
Journal:  Development       Date:  2012-10-03       Impact factor: 6.868

4.  Regulation of the Caenorhabditis elegans posterior Hox gene egl-5 by microRNA and the polycomb-like gene sop-2.

Authors:  Hongjie Zhang; Scott W Emmons
Journal:  Dev Dyn       Date:  2009-03       Impact factor: 3.780

5.  A genetic screen identifies novel polycomb group genes in Drosophila.

Authors:  Andrés Gaytán de Ayala Alonso; Luis Gutiérrez; Cornelia Fritsch; Bernadett Papp; Dirk Beuchle; Jürg Müller
Journal:  Genetics       Date:  2007-08       Impact factor: 4.562

6.  The Hox transcription factor Ubx stabilizes lineage commitment by suppressing cellular plasticity in Drosophila.

Authors:  Katrin Domsch; Julie Carnesecchi; Vanessa Disela; Jana Friedrich; Nils Trost; Olga Ermakova; Maria Polychronidou; Ingrid Lohmann
Journal:  Elife       Date:  2019-05-03       Impact factor: 8.140

7.  Trithorax monomethylates histone H3K4 and interacts directly with CBP to promote H3K27 acetylation and antagonize Polycomb silencing.

Authors:  Feng Tie; Rakhee Banerjee; Alina R Saiakhova; Benny Howard; Kelsey E Monteith; Peter C Scacheri; Michael S Cosgrove; Peter J Harte
Journal:  Development       Date:  2014-03       Impact factor: 6.868

Review 8.  Deconstructing repression: evolving models of co-repressor action.

Authors:  Valentina Perissi; Kristen Jepsen; Christopher K Glass; Michael G Rosenfeld
Journal:  Nat Rev Genet       Date:  2010-02       Impact factor: 53.242

9.  A region of the human HOXD cluster that confers polycomb-group responsiveness.

Authors:  Caroline J Woo; Peter V Kharchenko; Laurence Daheron; Peter J Park; Robert E Kingston
Journal:  Cell       Date:  2010-01-08       Impact factor: 41.582

10.  PcG recruitment by the YY1 REPO domain can be mediated by Yaf2.

Authors:  Frank Wilkinson; Heather Pratt; Michael L Atchison
Journal:  J Cell Biochem       Date:  2010-02-15       Impact factor: 4.429

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