Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Nature communications 2012-03, Vol.3 (1), p.717-717, Article 717
Main Authors: 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
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33
cites cdi_FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33
container_end_page 717
container_issue 1
container_start_page 717
container_title Nature communications
container_volume 3
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.
doi_str_mv 10.1038/ncomms1704
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_926878675</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>926878675</sourcerecordid><originalsourceid>FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33</originalsourceid><addsrcrecordid>eNptkdtKxDAQhoMoKuqNDyDBG0Gp5tCm6aUuHhZEQRS8K2kyXbO2ydq0Qn16I-sJcW5mYD7-mfkHoV1Kjinh8sRp37aB5iRdQZuMpDShOeOrv-oNtBPCnMTgBZVpuo42GONFJojcRPO7h5tHmlhnBg0GB9uA09bNsK-x8y5ph6AbwO3og3X4CdTriPWTivV0eoa1d31nq6GHgHuPW5ipZ9WNXo894IVvxkXjrbFvqrfebaO1WjUBdj7zFnq4OL-fXCXXt5fTyel1otOM9klVSGEk1QxUJuoC6lpJBqwiKtfxGiMLQWsGXDGTGpExzY2otFCE16KSFedb6GCpu-j8ywChL1sbNDSNcuCHUBZMyFyKPIvk_h9y7ofOxeXKIot-CSFZhA6XkO58CB3U5aKzbbyypKT8eEH584II730qDlUL5hv9MjwCR0sgxJabQfcz8h-5d7pEkqk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>950006682</pqid></control><display><type>article</type><title>RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization</title><source>Open Access: PubMed Central</source><source>Publicly Available Content (ProQuest)</source><source>Springer Nature - Connect here FIRST to enable access</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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. 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><subject>631/208/200</subject><subject>631/208/742</subject><subject>631/337/641/1655</subject><subject>692/698/233/1632</subject><subject>Animals</subject><subject>Antigens, CD34 - biosynthesis</subject><subject>Cell Line</subject><subject>Core Binding Factor Alpha 2 Subunit - genetics</subject><subject>Core Binding Factor Alpha 2 Subunit - metabolism</subject><subject>Cytokinesis</subject><subject>Heterocyclic Compounds, 4 or More Rings - pharmacology</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Megakaryocytes - cytology</subject><subject>Megakaryocytes - metabolism</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mitosis</subject><subject>multidisciplinary</subject><subject>Myosin Heavy Chains - biosynthesis</subject><subject>Myosin Heavy Chains - genetics</subject><subject>Myosin Heavy Chains - metabolism</subject><subject>Nonmuscle Myosin Type IIB - biosynthesis</subject><subject>Nonmuscle Myosin Type IIB - genetics</subject><subject>Nonmuscle Myosin Type IIB - metabolism</subject><subject>Polyploidy</subject><subject>RNA Interference</subject><subject>RNA, Small Interfering</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Transcription factors</subject><issn>2041-1723</issn><issn>2041-1723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkdtKxDAQhoMoKuqNDyDBG0Gp5tCm6aUuHhZEQRS8K2kyXbO2ydq0Qn16I-sJcW5mYD7-mfkHoV1Kjinh8sRp37aB5iRdQZuMpDShOeOrv-oNtBPCnMTgBZVpuo42GONFJojcRPO7h5tHmlhnBg0GB9uA09bNsK-x8y5ph6AbwO3og3X4CdTriPWTivV0eoa1d31nq6GHgHuPW5ipZ9WNXo894IVvxkXjrbFvqrfebaO1WjUBdj7zFnq4OL-fXCXXt5fTyel1otOM9klVSGEk1QxUJuoC6lpJBqwiKtfxGiMLQWsGXDGTGpExzY2otFCE16KSFedb6GCpu-j8ywChL1sbNDSNcuCHUBZMyFyKPIvk_h9y7ofOxeXKIot-CSFZhA6XkO58CB3U5aKzbbyypKT8eEH584II730qDlUL5hv9MjwCR0sgxJabQfcz8h-5d7pEkqk</recordid><startdate>20120306</startdate><enddate>20120306</enddate><creator>Lordier, Larissa</creator><creator>Bluteau, Dominique</creator><creator>Jalil, Abdelali</creator><creator>Legrand, Céline</creator><creator>Pan, Jiajia</creator><creator>Rameau, Philippe</creator><creator>Jouni, Dima</creator><creator>Bluteau, Olivier</creator><creator>Mercher, Thomas</creator><creator>Leon, Catherine</creator><creator>Gachet, Christian</creator><creator>Debili, Najet</creator><creator>Vainchenker, William</creator><creator>Raslova, Hana</creator><creator>Chang, Yunhua</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>20120306</creationdate><title>RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>631/208/200</topic><topic>631/208/742</topic><topic>631/337/641/1655</topic><topic>692/698/233/1632</topic><topic>Animals</topic><topic>Antigens, CD34 - biosynthesis</topic><topic>Cell Line</topic><topic>Core Binding Factor Alpha 2 Subunit - genetics</topic><topic>Core Binding Factor Alpha 2 Subunit - metabolism</topic><topic>Cytokinesis</topic><topic>Heterocyclic Compounds, 4 or More Rings - pharmacology</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Megakaryocytes - cytology</topic><topic>Megakaryocytes - metabolism</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Mitosis</topic><topic>multidisciplinary</topic><topic>Myosin Heavy Chains - biosynthesis</topic><topic>Myosin Heavy Chains - genetics</topic><topic>Myosin Heavy Chains - metabolism</topic><topic>Nonmuscle Myosin Type IIB - biosynthesis</topic><topic>Nonmuscle Myosin Type IIB - genetics</topic><topic>Nonmuscle Myosin Type IIB - metabolism</topic><topic>Polyploidy</topic><topic>RNA Interference</topic><topic>RNA, Small Interfering</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; Medical Collection (ProQuest Medical &amp; Health Databases)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lordier, Larissa</au><au>Bluteau, Dominique</au><au>Jalil, Abdelali</au><au>Legrand, Céline</au><au>Pan, Jiajia</au><au>Rameau, Philippe</au><au>Jouni, Dima</au><au>Bluteau, Olivier</au><au>Mercher, Thomas</au><au>Leon, Catherine</au><au>Gachet, Christian</au><au>Debili, Najet</au><au>Vainchenker, William</au><au>Raslova, Hana</au><au>Chang, Yunhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat 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>
fulltext fulltext
identifier ISSN: 2041-1723
ispartof Nature communications, 2012-03, Vol.3 (1), p.717-717, Article 717
issn 2041-1723
2041-1723
language eng
recordid cdi_proquest_miscellaneous_926878675
source Open Access: PubMed Central; Publicly Available Content (ProQuest); Springer Nature - Connect here FIRST to enable access; Springer Nature - nature.com Journals - Fully Open Access
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T23%3A40%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=RUNX1-induced%20silencing%20of%20non-muscle%20myosin%20heavy%20chain%20IIB%20contributes%20to%20megakaryocyte%20polyploidization&rft.jtitle=Nature%20communications&rft.au=Lordier,%20Larissa&rft.date=2012-03-06&rft.volume=3&rft.issue=1&rft.spage=717&rft.epage=717&rft.pages=717-717&rft.artnum=717&rft.issn=2041-1723&rft.eissn=2041-1723&rft_id=info:doi/10.1038/ncomms1704&rft_dat=%3Cproquest_cross%3E926878675%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c451t-b986d81c2ea56f9effa82e2b0a7c723d8961f2e3a2d4d652c3d6bc6a03f6b8b33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=950006682&rft_id=info:pmid/22395608&rfr_iscdi=true