Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development
Although it is known that the tetraploid embryo contributes only to the placenta, the question of why tetraploid embryos differentiate into placenta remains unclear. To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two‐cell embryos were fused and cultured in...
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Veröffentlicht in: | Developmental dynamics 2011-07, Vol.240 (7), p.1660-1669 |
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creator | Park, Mi‐Ryung Lee, Ah‐Reum Bui, Hong‐Thuy Park, Chankyu Park, Keun‐Kyu Cho, Ssang‐Goo Song, Hyuk Kim, Jae‐Hwan Van Thuan, Nguyen Kim, Jin‐Hoi |
description | Although it is known that the tetraploid embryo contributes only to the placenta, the question of why tetraploid embryos differentiate into placenta remains unclear. To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two‐cell embryos were fused and cultured in vitro in Chatot‐Ziomek‐Bavister medium. After electrofusion, two chromosome sets from the tetraploid blastomere were individually duplicated before nuclear fusion. At 8–10 hr after electrofusion, each chromosome set was condensing and the nuclear membrane was breaking down. Around 12–14 hr after electrofusion, the two chromosome sets had combined together and had reached the second mitotic metaphase, at this point with 8n sets of chromosomes. Interestingly, we discovered that expression of OCT4, an inner cell mass cells biomarker, is lost by the tetraploid expanded blastocysts, but that CDX2, a trophectoderm cells biomarker, is strongly expressed at this stage. This observation provides evidence clarifying why tetraploid embryos contribute only to trophectoderm. Developmental Dynamics 240:1660–1669, 2011. © 2011 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/dvdy.22653 |
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To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two‐cell embryos were fused and cultured in vitro in Chatot‐Ziomek‐Bavister medium. After electrofusion, two chromosome sets from the tetraploid blastomere were individually duplicated before nuclear fusion. At 8–10 hr after electrofusion, each chromosome set was condensing and the nuclear membrane was breaking down. Around 12–14 hr after electrofusion, the two chromosome sets had combined together and had reached the second mitotic metaphase, at this point with 8n sets of chromosomes. Interestingly, we discovered that expression of OCT4, an inner cell mass cells biomarker, is lost by the tetraploid expanded blastocysts, but that CDX2, a trophectoderm cells biomarker, is strongly expressed at this stage. This observation provides evidence clarifying why tetraploid embryos contribute only to trophectoderm. Developmental Dynamics 240:1660–1669, 2011. © 2011 Wiley‐Liss, Inc.</description><identifier>ISSN: 1058-8388</identifier><identifier>EISSN: 1097-0177</identifier><identifier>DOI: 10.1002/dvdy.22653</identifier><identifier>PMID: 21547981</identifier><language>eng</language><publisher>New York: Wiley‐Liss, Inc</publisher><subject>Animals ; Blastocyst - cytology ; Blastocyst - metabolism ; Cdx2 ; CDX2 Transcription Factor ; Cell Differentiation - genetics ; Cell Differentiation - physiology ; Chromosomes - metabolism ; chromosomes remodeling ; Embryonic Development - genetics ; Embryonic Development - physiology ; Female ; first differentiation ; Homeodomain Proteins - metabolism ; Karyotyping ; Male ; Mice ; Oct4 ; Octamer Transcription Factor-3 - metabolism ; Pregnancy ; preimplantation development ; tetraploid embryos ; Tetraploidy ; Transcription Factors - metabolism</subject><ispartof>Developmental dynamics, 2011-07, Vol.240 (7), p.1660-1669</ispartof><rights>Copyright © 2011 Wiley‐Liss, Inc.</rights><rights>Copyright © 2011 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4303-6dba4ce8a877102a8fe7b0f5c132a692371fbea8f1a8352b5b043eff2265e3b13</citedby><cites>FETCH-LOGICAL-c4303-6dba4ce8a877102a8fe7b0f5c132a692371fbea8f1a8352b5b043eff2265e3b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdvdy.22653$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdvdy.22653$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,1434,27928,27929,45578,45579,46413,46837</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21547981$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Mi‐Ryung</creatorcontrib><creatorcontrib>Lee, Ah‐Reum</creatorcontrib><creatorcontrib>Bui, Hong‐Thuy</creatorcontrib><creatorcontrib>Park, Chankyu</creatorcontrib><creatorcontrib>Park, Keun‐Kyu</creatorcontrib><creatorcontrib>Cho, Ssang‐Goo</creatorcontrib><creatorcontrib>Song, Hyuk</creatorcontrib><creatorcontrib>Kim, Jae‐Hwan</creatorcontrib><creatorcontrib>Van Thuan, Nguyen</creatorcontrib><creatorcontrib>Kim, Jin‐Hoi</creatorcontrib><title>Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development</title><title>Developmental dynamics</title><addtitle>Dev Dyn</addtitle><description>Although it is known that the tetraploid embryo contributes only to the placenta, the question of why tetraploid embryos differentiate into placenta remains unclear. To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two‐cell embryos were fused and cultured in vitro in Chatot‐Ziomek‐Bavister medium. After electrofusion, two chromosome sets from the tetraploid blastomere were individually duplicated before nuclear fusion. At 8–10 hr after electrofusion, each chromosome set was condensing and the nuclear membrane was breaking down. Around 12–14 hr after electrofusion, the two chromosome sets had combined together and had reached the second mitotic metaphase, at this point with 8n sets of chromosomes. Interestingly, we discovered that expression of OCT4, an inner cell mass cells biomarker, is lost by the tetraploid expanded blastocysts, but that CDX2, a trophectoderm cells biomarker, is strongly expressed at this stage. This observation provides evidence clarifying why tetraploid embryos contribute only to trophectoderm. Developmental Dynamics 240:1660–1669, 2011. © 2011 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Blastocyst - cytology</subject><subject>Blastocyst - metabolism</subject><subject>Cdx2</subject><subject>CDX2 Transcription Factor</subject><subject>Cell Differentiation - genetics</subject><subject>Cell Differentiation - physiology</subject><subject>Chromosomes - metabolism</subject><subject>chromosomes remodeling</subject><subject>Embryonic Development - genetics</subject><subject>Embryonic Development - physiology</subject><subject>Female</subject><subject>first differentiation</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Karyotyping</subject><subject>Male</subject><subject>Mice</subject><subject>Oct4</subject><subject>Octamer Transcription Factor-3 - metabolism</subject><subject>Pregnancy</subject><subject>preimplantation development</subject><subject>tetraploid embryos</subject><subject>Tetraploidy</subject><subject>Transcription Factors - metabolism</subject><issn>1058-8388</issn><issn>1097-0177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMo7rp68QdIb4LQNR_tJnuUXb9A8KKCp5I0E400TU3alf33tnb16GmG4ZmHmRehU4LnBGN6qTd6O6d0kbM9NCV4yVNMON8f-lykggkxQUcxfmCMxSIjh2hCSZ7xpSBTpFbvwTsfvYMkgPMaKlu_JbLWibbGQIC6tbK1vk68SVpog2wqb3UCToWtj4nuwrDQBLCuqWTdjrCGDVS-cf36MTowsopwsqsz9Hxz_bS6Sx8eb-9XVw9pmTHM0oVWMitBSME5wVQKA1xhk5eEUblYUsaJUdCPiRQspypXOGNgzPA4MEXYDJ2P3ib4zw5iWzgbS6j6o8B3sRCcEsoFFj15MZJl8DEGMEUTrJNhWxBcDJEWQ6TFT6Q9fLbTdsqB_kN_M-wBMgJftoLtP6pi_bJ-HaXfQEyEPQ</recordid><startdate>201107</startdate><enddate>201107</enddate><creator>Park, Mi‐Ryung</creator><creator>Lee, Ah‐Reum</creator><creator>Bui, Hong‐Thuy</creator><creator>Park, Chankyu</creator><creator>Park, Keun‐Kyu</creator><creator>Cho, Ssang‐Goo</creator><creator>Song, Hyuk</creator><creator>Kim, Jae‐Hwan</creator><creator>Van Thuan, Nguyen</creator><creator>Kim, Jin‐Hoi</creator><general>Wiley‐Liss, Inc</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>7X8</scope></search><sort><creationdate>201107</creationdate><title>Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development</title><author>Park, Mi‐Ryung ; Lee, Ah‐Reum ; Bui, Hong‐Thuy ; Park, Chankyu ; Park, Keun‐Kyu ; Cho, Ssang‐Goo ; Song, Hyuk ; Kim, Jae‐Hwan ; Van Thuan, Nguyen ; Kim, Jin‐Hoi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4303-6dba4ce8a877102a8fe7b0f5c132a692371fbea8f1a8352b5b043eff2265e3b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Blastocyst - cytology</topic><topic>Blastocyst - metabolism</topic><topic>Cdx2</topic><topic>CDX2 Transcription Factor</topic><topic>Cell Differentiation - genetics</topic><topic>Cell Differentiation - physiology</topic><topic>Chromosomes - metabolism</topic><topic>chromosomes remodeling</topic><topic>Embryonic Development - genetics</topic><topic>Embryonic Development - physiology</topic><topic>Female</topic><topic>first differentiation</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Karyotyping</topic><topic>Male</topic><topic>Mice</topic><topic>Oct4</topic><topic>Octamer Transcription Factor-3 - metabolism</topic><topic>Pregnancy</topic><topic>preimplantation development</topic><topic>tetraploid embryos</topic><topic>Tetraploidy</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Mi‐Ryung</creatorcontrib><creatorcontrib>Lee, Ah‐Reum</creatorcontrib><creatorcontrib>Bui, Hong‐Thuy</creatorcontrib><creatorcontrib>Park, Chankyu</creatorcontrib><creatorcontrib>Park, Keun‐Kyu</creatorcontrib><creatorcontrib>Cho, Ssang‐Goo</creatorcontrib><creatorcontrib>Song, Hyuk</creatorcontrib><creatorcontrib>Kim, Jae‐Hwan</creatorcontrib><creatorcontrib>Van Thuan, Nguyen</creatorcontrib><creatorcontrib>Kim, Jin‐Hoi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Mi‐Ryung</au><au>Lee, Ah‐Reum</au><au>Bui, Hong‐Thuy</au><au>Park, Chankyu</au><au>Park, Keun‐Kyu</au><au>Cho, Ssang‐Goo</au><au>Song, Hyuk</au><au>Kim, Jae‐Hwan</au><au>Van Thuan, Nguyen</au><au>Kim, Jin‐Hoi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development</atitle><jtitle>Developmental dynamics</jtitle><addtitle>Dev Dyn</addtitle><date>2011-07</date><risdate>2011</risdate><volume>240</volume><issue>7</issue><spage>1660</spage><epage>1669</epage><pages>1660-1669</pages><issn>1058-8388</issn><eissn>1097-0177</eissn><abstract>Although it is known that the tetraploid embryo contributes only to the placenta, the question of why tetraploid embryos differentiate into placenta remains unclear. To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two‐cell embryos were fused and cultured in vitro in Chatot‐Ziomek‐Bavister medium. After electrofusion, two chromosome sets from the tetraploid blastomere were individually duplicated before nuclear fusion. At 8–10 hr after electrofusion, each chromosome set was condensing and the nuclear membrane was breaking down. Around 12–14 hr after electrofusion, the two chromosome sets had combined together and had reached the second mitotic metaphase, at this point with 8n sets of chromosomes. Interestingly, we discovered that expression of OCT4, an inner cell mass cells biomarker, is lost by the tetraploid expanded blastocysts, but that CDX2, a trophectoderm cells biomarker, is strongly expressed at this stage. This observation provides evidence clarifying why tetraploid embryos contribute only to trophectoderm. 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subjects | Animals Blastocyst - cytology Blastocyst - metabolism Cdx2 CDX2 Transcription Factor Cell Differentiation - genetics Cell Differentiation - physiology Chromosomes - metabolism chromosomes remodeling Embryonic Development - genetics Embryonic Development - physiology Female first differentiation Homeodomain Proteins - metabolism Karyotyping Male Mice Oct4 Octamer Transcription Factor-3 - metabolism Pregnancy preimplantation development tetraploid embryos Tetraploidy Transcription Factors - metabolism |
title | Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development |
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