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RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization
Megakaryocytes are unique mammalian cells that undergo polyploidization (endomitosis) during differentiation, leading to an increase in cell size and protein production that precedes platelet production. Recent evidence demonstrates that endomitosis is a consequence of a late failure in cytokinesis...
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Published in: | Nature communications 2012-03, Vol.3 (1), p.717-717, Article 717 |
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creator | Lordier, Larissa Bluteau, Dominique Jalil, Abdelali Legrand, Céline Pan, Jiajia Rameau, Philippe Jouni, Dima Bluteau, Olivier Mercher, Thomas Leon, Catherine Gachet, Christian Debili, Najet Vainchenker, William Raslova, Hana Chang, Yunhua |
description | Megakaryocytes are unique mammalian cells that undergo polyploidization (endomitosis) during differentiation, leading to an increase in cell size and protein production that precedes platelet production. Recent evidence demonstrates that endomitosis is a consequence of a late failure in cytokinesis associated with a contractile ring defect. Here we show that the non-muscle myosin IIB heavy chain (MYH10) is expressed in immature megakaryocytes and specifically localizes in the contractile ring. MYH10 downmodulation by short hairpin RNA increases polyploidization by inhibiting the return of 4N cells to 2N, but other regulators, such as of the G1/S transition, might regulate further polyploidization of the 4N cells. Conversely, re-expression of MYH10 in the megakaryocytes prevents polyploidization and the transition of 2N to 4N cells. During polyploidization, MYH10 expression is repressed by the major megakaryocyte transcription factor RUNX1. Thus, RUNX1-mediated silencing of MYH10 is required for the switch from mitosis to endomitosis, linking polyploidization with megakaryocyte differentiation.
Megakaryocytes undergo polyploidization prior to forming platelets but this process is poorly characterised. In this study, non-muscle myosin IIB heavy chain, that localizes to the contractile ring during mitosis, is shown to be silenced prior to polyploidization in a RUNX1-dependent manner. |
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Megakaryocytes undergo polyploidization prior to forming platelets but this process is poorly characterised. In this study, non-muscle myosin IIB heavy chain, that localizes to the contractile ring during mitosis, is shown to be silenced prior to polyploidization in a RUNX1-dependent manner.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/ncomms1704</identifier><identifier>PMID: 22395608</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/208/200 ; 631/208/742 ; 631/337/641/1655 ; 692/698/233/1632 ; Animals ; Antigens, CD34 - biosynthesis ; Cell Line ; Core Binding Factor Alpha 2 Subunit - genetics ; Core Binding Factor Alpha 2 Subunit - metabolism ; Cytokinesis ; Heterocyclic Compounds, 4 or More Rings - pharmacology ; Humanities and Social Sciences ; Humans ; Megakaryocytes - cytology ; Megakaryocytes - metabolism ; Mice ; Mice, Knockout ; Mitosis ; multidisciplinary ; Myosin Heavy Chains - biosynthesis ; Myosin Heavy Chains - genetics ; Myosin Heavy Chains - metabolism ; Nonmuscle Myosin Type IIB - biosynthesis ; Nonmuscle Myosin Type IIB - genetics ; Nonmuscle Myosin Type IIB - metabolism ; Polyploidy ; RNA Interference ; RNA, Small Interfering ; Science ; Science (multidisciplinary) ; Transcription factors</subject><ispartof>Nature communications, 2012-03, Vol.3 (1), p.717-717, Article 717</ispartof><rights>Springer Nature Limited 2012</rights><rights>Copyright Nature Publishing Group Mar 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33</citedby><cites>FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/950006682/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/950006682?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22395608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lordier, Larissa</creatorcontrib><creatorcontrib>Bluteau, Dominique</creatorcontrib><creatorcontrib>Jalil, Abdelali</creatorcontrib><creatorcontrib>Legrand, Céline</creatorcontrib><creatorcontrib>Pan, Jiajia</creatorcontrib><creatorcontrib>Rameau, Philippe</creatorcontrib><creatorcontrib>Jouni, Dima</creatorcontrib><creatorcontrib>Bluteau, Olivier</creatorcontrib><creatorcontrib>Mercher, Thomas</creatorcontrib><creatorcontrib>Leon, Catherine</creatorcontrib><creatorcontrib>Gachet, Christian</creatorcontrib><creatorcontrib>Debili, Najet</creatorcontrib><creatorcontrib>Vainchenker, William</creatorcontrib><creatorcontrib>Raslova, Hana</creatorcontrib><creatorcontrib>Chang, Yunhua</creatorcontrib><title>RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>Megakaryocytes are unique mammalian cells that undergo polyploidization (endomitosis) during differentiation, leading to an increase in cell size and protein production that precedes platelet production. Recent evidence demonstrates that endomitosis is a consequence of a late failure in cytokinesis associated with a contractile ring defect. Here we show that the non-muscle myosin IIB heavy chain (MYH10) is expressed in immature megakaryocytes and specifically localizes in the contractile ring. MYH10 downmodulation by short hairpin RNA increases polyploidization by inhibiting the return of 4N cells to 2N, but other regulators, such as of the G1/S transition, might regulate further polyploidization of the 4N cells. Conversely, re-expression of MYH10 in the megakaryocytes prevents polyploidization and the transition of 2N to 4N cells. During polyploidization, MYH10 expression is repressed by the major megakaryocyte transcription factor RUNX1. Thus, RUNX1-mediated silencing of MYH10 is required for the switch from mitosis to endomitosis, linking polyploidization with megakaryocyte differentiation.
Megakaryocytes undergo polyploidization prior to forming platelets but this process is poorly characterised. 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Commun</addtitle><date>2012-03-06</date><risdate>2012</risdate><volume>3</volume><issue>1</issue><spage>717</spage><epage>717</epage><pages>717-717</pages><artnum>717</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Megakaryocytes are unique mammalian cells that undergo polyploidization (endomitosis) during differentiation, leading to an increase in cell size and protein production that precedes platelet production. Recent evidence demonstrates that endomitosis is a consequence of a late failure in cytokinesis associated with a contractile ring defect. Here we show that the non-muscle myosin IIB heavy chain (MYH10) is expressed in immature megakaryocytes and specifically localizes in the contractile ring. MYH10 downmodulation by short hairpin RNA increases polyploidization by inhibiting the return of 4N cells to 2N, but other regulators, such as of the G1/S transition, might regulate further polyploidization of the 4N cells. Conversely, re-expression of MYH10 in the megakaryocytes prevents polyploidization and the transition of 2N to 4N cells. During polyploidization, MYH10 expression is repressed by the major megakaryocyte transcription factor RUNX1. Thus, RUNX1-mediated silencing of MYH10 is required for the switch from mitosis to endomitosis, linking polyploidization with megakaryocyte differentiation.
Megakaryocytes undergo polyploidization prior to forming platelets but this process is poorly characterised. In this study, non-muscle myosin IIB heavy chain, that localizes to the contractile ring during mitosis, is shown to be silenced prior to polyploidization in a RUNX1-dependent manner.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>22395608</pmid><doi>10.1038/ncomms1704</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/208/200 631/208/742 631/337/641/1655 692/698/233/1632 Animals Antigens, CD34 - biosynthesis Cell Line Core Binding Factor Alpha 2 Subunit - genetics Core Binding Factor Alpha 2 Subunit - metabolism Cytokinesis Heterocyclic Compounds, 4 or More Rings - pharmacology Humanities and Social Sciences Humans Megakaryocytes - cytology Megakaryocytes - metabolism Mice Mice, Knockout Mitosis multidisciplinary Myosin Heavy Chains - biosynthesis Myosin Heavy Chains - genetics Myosin Heavy Chains - metabolism Nonmuscle Myosin Type IIB - biosynthesis Nonmuscle Myosin Type IIB - genetics Nonmuscle Myosin Type IIB - metabolism Polyploidy RNA Interference RNA, Small Interfering Science Science (multidisciplinary) Transcription factors |
title | RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization |
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