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<span id="openzim-page-title" class="mw-page-title-main"><span class="mw-page-title-main">PRC2</span></span>
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<p><b>PRC2</b> (<b>polycomb repressive complex 2</b>) is one of the two classes of <a href="Polycomb-group_proteins" title="Polycomb-group proteins">polycomb-group proteins</a> or (PcG). The other component of this group of proteins is PRC1 (<a href="Polycomb_repressive_complex_1" title="Polycomb repressive complex 1">Polycomb Repressive Complex 1</a>).
</p><p>This complex has <a href="Histone" title="Histone">histone</a> <a href="Methyltransferase" title="Methyltransferase">methyltransferase</a> activity and primarily methylates <a href="Histone_H3" title="Histone H3">histone H3</a> on <a href="Lysine" title="Lysine">lysine</a> 27 (i.e. <a href="H3K27me3" title="H3K27me3">H3K27me3</a>),<sup id="cite_ref-pmid22211105_1-0" class="reference"><a href="#cite_note-pmid22211105-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid21367748_2-0" class="reference"><a href="#cite_note-pmid21367748-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> a mark of transcriptionally silent <a href="Chromatin" title="Chromatin">chromatin</a>. PRC2 is required for initial targeting of genomic region (PRC Response Elements or PRE) to be silenced, while PRC1 is required for stabilizing this <a href="Gene_silencing" title="Gene silencing">silencing</a> and underlies <a href="Epigenetics" title="Epigenetics">cellular memory</a> of silenced region after <a href="Cellular_differentiation" title="Cellular differentiation">cellular differentiation</a>. PRC1 also <a href="Mono-ubiquitinate" class="mw-redirect" title="Mono-ubiquitinate">mono-ubiquitinates</a> <a href="Histone_H2A" title="Histone H2A">histone H2A</a> on lysine 119 (H2AK119Ub1). These <a href="Protein" title="Protein">proteins</a> are required for long term epigenetic silencing of chromatin and have an important role in <a href="Stem_cell" title="Stem cell">stem cell</a> differentiation and early <a href="Embryo" title="Embryo">embryonic</a> development. PRC2 are present in most <a href="Multicellular_organism" title="Multicellular organism">multicellular organisms</a>.
</p><p>The mouse PRC2 has four subunits: <a href="SUZ12" title="SUZ12">Suz12</a> (<a href="Zinc_finger" title="Zinc finger">zinc finger</a>), <a href="Polycomb_protein_EED" title="Polycomb protein EED">Eed</a>, <a href="Ezh1" class="mw-redirect" title="Ezh1">Ezh1</a> or <a href="Ezh2" class="mw-redirect" title="Ezh2">Ezh2</a> (<a href="SET_domain" title="SET domain">SET domain</a> with histone methyltransferase activity<sup id="cite_ref-pmid22211105_1-1" class="reference"><a href="#cite_note-pmid22211105-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid21367748_2-1" class="reference"><a href="#cite_note-pmid21367748-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>) and <a href="Rbbp4" class="mw-redirect" title="Rbbp4">Rbbp4</a> (histone <a href="Binding_domain" title="Binding domain">binding domain</a>). PRC2 can bind to H3K27me3 and repress neighboring <a href="Nucleosome" title="Nucleosome">nucleosomes</a>, thus spreading the repression.<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p><p>PRC2 has a role in <a href="X_chromosome_inactivation" class="mw-redirect" title="X chromosome inactivation">X chromosome inactivation</a>, in maintenance of stem cell fate,<sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> and in imprinting. Aberrant expression of PRC2 has been observed in <a href="Cancer" title="Cancer">cancer</a>.<sup id="cite_ref-pmid22211105_1-2" class="reference"><a href="#cite_note-pmid22211105-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid21367748_2-2" class="reference"><a href="#cite_note-pmid21367748-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> Both loss and gain-of-function mutations in PRC2 components have been identified in various human <a href="Cancer_epigenetics" title="Cancer epigenetics">cancers</a>, suggesting complex roles of these components in malignancy.<sup id="cite_ref-pmid28758948_5-0" class="reference"><a href="#cite_note-pmid28758948-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup>
</p><p>Polycomb group genes directly and indirectly regulate the <a href="DNA_damage_(naturally_occurring)" title="DNA damage (naturally occurring)">DNA damage</a> response which acts as an anti-cancer barrier.<sup id="cite_ref-pmid28758948_5-1" class="reference"><a href="#cite_note-pmid28758948-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> The PRC2 complex appears to be present at sites of DNA double-strand breaks where it promotes repair of such breaks by <a href="Non-homologous_end_joining" title="Non-homologous end joining">non-homologous end joining</a>.<sup id="cite_ref-pmid28758948_5-2" class="reference"><a href="#cite_note-pmid28758948-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup>
</p><p>The PRC2 is <a href="Common_descent" title="Common descent">evolutionarily conserved</a>, and has been found in mammals, insects, fungi, and plants.
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<div class="mw-heading mw-heading2"><h2 id="In_plants">In plants</h2></div>
<p>In <i><a href="Arabidopsis_thaliana" title="Arabidopsis thaliana">Arabidopsis thaliana</a></i>, a plant <a href="Model_organism" title="Model organism">model organism</a>, several variants of the core subunits have been identified. <a href="Homologous_chromosomes" class="mw-redirect" title="Homologous chromosomes">Homologs</a> of the Suz12 subunit are: Embryonic flower 2 (EMF2), reduced vernalization response 2 (VRN2), fertilization independent seed 2 (FIS2).<sup id="cite_ref-Köhler_and_Hennig_2010_6-0" class="reference"><a href="#cite_note-Köhler_and_Hennig_2010-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> There is one Eed homolog, fertilization independent endosperm (FIE).<sup id="cite_ref-Köhler_and_Hennig_2010_6-1" class="reference"><a href="#cite_note-Köhler_and_Hennig_2010-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> three Ezh1/Ezh2 homologs, curly leaf (CLF), swinger (SWN), medea (MEA),<sup id="cite_ref-Köhler_and_Hennig_2010_6-2" class="reference"><a href="#cite_note-Köhler_and_Hennig_2010-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> and one Rbbp4 homolog, multicopy suppressor of IRA1 (MSI1).<sup id="cite_ref-Köhler_and_Hennig_2010_6-3" class="reference"><a href="#cite_note-Köhler_and_Hennig_2010-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> Many other accessory components of PRC2 complex in Arabidopsis have been identified<a rel="nofollow" class="external autonumber" href="https://www.mdpi.com/2075-4655/6/1/8">[1]</a>.
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<div class="mw-heading mw-heading2"><h2 id="See_also">See also</h2></div>
<ul><li><a href="Epigenetics" title="Epigenetics">Epigenetics</a></li></ul>
<div class="mw-heading mw-heading2"><h2 id="References">References</h2></div>
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