Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig

The inner cell mass (ICM) in blastocyst is the origin of all somatic and germ cells in mammals and pluripotent stem cells (PSCs) in vitro. As the conserved principles between pig and human, here we performed comprehensive single‐cell RNA‐seq for porcine early embryos from oocyte to early blastocyst...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The FASEB journal 2020-01, Vol.34 (1), p.691-705
Hauptverfasser: Kong, Qingran, Yang, Xu, Zhang, Heng, Liu, Shichao, Zhao, Jianchao, Zhang, Jiaming, Weng, Xiaogang, Jin, Junxue, Liu, Zhonghua
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 705
container_issue 1
container_start_page 691
container_title The FASEB journal
container_volume 34
creator Kong, Qingran
Yang, Xu
Zhang, Heng
Liu, Shichao
Zhao, Jianchao
Zhang, Jiaming
Weng, Xiaogang
Jin, Junxue
Liu, Zhonghua
description The inner cell mass (ICM) in blastocyst is the origin of all somatic and germ cells in mammals and pluripotent stem cells (PSCs) in vitro. As the conserved principles between pig and human, here we performed comprehensive single‐cell RNA‐seq for porcine early embryos from oocyte to early blastocyst (EB). We show the specification of the ICM and trophectoderm in morula and the molecular signature of the precursors. We demonstrate the existence of naïve pluripotency signature in morula and ICM of EB, and the specific pluripotent genes and the activity of signalling pathways highlight the characteristics of the naïve pluripotency. We observe the absence of dosage compensation with respect to X‐chromosome (XC) in morula, and incomplete dosage compensation in the EB. However, the dynamics of dosage compensation may be independent of the expression of XIST induced XC inactivation. Our study describes molecular landmarks of embryogenesis in pig that will provide a better strategy for derivation of porcine PSCs and improve research in regenerative medicine.
doi_str_mv 10.1096/fj.201901818RR
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2335173802</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2335173802</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3818-6b8a440aa644dc49b70f9b665532240854150051a0509c09aa8bb12c922283ca3</originalsourceid><addsrcrecordid>eNqFkE1LxDAQhoMoun5cPUqOXrpOkiYmRxW_YEHw41ym2VSytE1Nskr_vZVV8eZpGOZ5X5iHkGMGcwZGnTWrOQdmgGmmHx-3yIxJAYXSCrbJDLThhVJC75H9lFYAwICpXbInmGGl4mpGVgvfO3x1NA3O-sZbzD70FPslHdp19EPIrrcjje7dYeuWtB5pjtgnO91y6NyEYjsmn2gTQ0dDsGN2NAdat5jytKVMfU8H_3pIdhpskzv6ngfk5eb6-equWDzc3l9dLAorpicKVWssS0BUZbm0panPoTG1UlIKzkvQsmQSQDIECcaCQdR1zbg1nHMtLIoDcrrpHWJ4W7uUq84n69oWexfWqeJCSHYuNPAJnW9QG0NK0TXVEH2HcawYVF9-q2ZV_fE7BU6-u9d155a_-I_QCZAb4MO3bvynrrp5uuQcQGjxCYCfhr4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2335173802</pqid></control><display><type>article</type><title>Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Alma/SFX Local Collection</source><creator>Kong, Qingran ; Yang, Xu ; Zhang, Heng ; Liu, Shichao ; Zhao, Jianchao ; Zhang, Jiaming ; Weng, Xiaogang ; Jin, Junxue ; Liu, Zhonghua</creator><creatorcontrib>Kong, Qingran ; Yang, Xu ; Zhang, Heng ; Liu, Shichao ; Zhao, Jianchao ; Zhang, Jiaming ; Weng, Xiaogang ; Jin, Junxue ; Liu, Zhonghua</creatorcontrib><description>The inner cell mass (ICM) in blastocyst is the origin of all somatic and germ cells in mammals and pluripotent stem cells (PSCs) in vitro. As the conserved principles between pig and human, here we performed comprehensive single‐cell RNA‐seq for porcine early embryos from oocyte to early blastocyst (EB). We show the specification of the ICM and trophectoderm in morula and the molecular signature of the precursors. We demonstrate the existence of naïve pluripotency signature in morula and ICM of EB, and the specific pluripotent genes and the activity of signalling pathways highlight the characteristics of the naïve pluripotency. We observe the absence of dosage compensation with respect to X‐chromosome (XC) in morula, and incomplete dosage compensation in the EB. However, the dynamics of dosage compensation may be independent of the expression of XIST induced XC inactivation. Our study describes molecular landmarks of embryogenesis in pig that will provide a better strategy for derivation of porcine PSCs and improve research in regenerative medicine.</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.201901818RR</identifier><identifier>PMID: 31914626</identifier><language>eng</language><publisher>United States</publisher><subject>mammals ; pig ; preimplantation embryonic development ; single‐cell RNA‐seq ; transcriptome</subject><ispartof>The FASEB journal, 2020-01, Vol.34 (1), p.691-705</ispartof><rights>2019 Federation of American Societies for Experimental Biology</rights><rights>2019 Federation of American Societies for Experimental Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3818-6b8a440aa644dc49b70f9b665532240854150051a0509c09aa8bb12c922283ca3</citedby><cites>FETCH-LOGICAL-c3818-6b8a440aa644dc49b70f9b665532240854150051a0509c09aa8bb12c922283ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1096%2Ffj.201901818RR$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1096%2Ffj.201901818RR$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31914626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kong, Qingran</creatorcontrib><creatorcontrib>Yang, Xu</creatorcontrib><creatorcontrib>Zhang, Heng</creatorcontrib><creatorcontrib>Liu, Shichao</creatorcontrib><creatorcontrib>Zhao, Jianchao</creatorcontrib><creatorcontrib>Zhang, Jiaming</creatorcontrib><creatorcontrib>Weng, Xiaogang</creatorcontrib><creatorcontrib>Jin, Junxue</creatorcontrib><creatorcontrib>Liu, Zhonghua</creatorcontrib><title>Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><description>The inner cell mass (ICM) in blastocyst is the origin of all somatic and germ cells in mammals and pluripotent stem cells (PSCs) in vitro. As the conserved principles between pig and human, here we performed comprehensive single‐cell RNA‐seq for porcine early embryos from oocyte to early blastocyst (EB). We show the specification of the ICM and trophectoderm in morula and the molecular signature of the precursors. We demonstrate the existence of naïve pluripotency signature in morula and ICM of EB, and the specific pluripotent genes and the activity of signalling pathways highlight the characteristics of the naïve pluripotency. We observe the absence of dosage compensation with respect to X‐chromosome (XC) in morula, and incomplete dosage compensation in the EB. However, the dynamics of dosage compensation may be independent of the expression of XIST induced XC inactivation. Our study describes molecular landmarks of embryogenesis in pig that will provide a better strategy for derivation of porcine PSCs and improve research in regenerative medicine.</description><subject>mammals</subject><subject>pig</subject><subject>preimplantation embryonic development</subject><subject>single‐cell RNA‐seq</subject><subject>transcriptome</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMoun5cPUqOXrpOkiYmRxW_YEHw41ym2VSytE1Nskr_vZVV8eZpGOZ5X5iHkGMGcwZGnTWrOQdmgGmmHx-3yIxJAYXSCrbJDLThhVJC75H9lFYAwICpXbInmGGl4mpGVgvfO3x1NA3O-sZbzD70FPslHdp19EPIrrcjje7dYeuWtB5pjtgnO91y6NyEYjsmn2gTQ0dDsGN2NAdat5jytKVMfU8H_3pIdhpskzv6ngfk5eb6-equWDzc3l9dLAorpicKVWssS0BUZbm0panPoTG1UlIKzkvQsmQSQDIECcaCQdR1zbg1nHMtLIoDcrrpHWJ4W7uUq84n69oWexfWqeJCSHYuNPAJnW9QG0NK0TXVEH2HcawYVF9-q2ZV_fE7BU6-u9d155a_-I_QCZAb4MO3bvynrrp5uuQcQGjxCYCfhr4</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Kong, Qingran</creator><creator>Yang, Xu</creator><creator>Zhang, Heng</creator><creator>Liu, Shichao</creator><creator>Zhao, Jianchao</creator><creator>Zhang, Jiaming</creator><creator>Weng, Xiaogang</creator><creator>Jin, Junxue</creator><creator>Liu, Zhonghua</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202001</creationdate><title>Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig</title><author>Kong, Qingran ; Yang, Xu ; Zhang, Heng ; Liu, Shichao ; Zhao, Jianchao ; Zhang, Jiaming ; Weng, Xiaogang ; Jin, Junxue ; Liu, Zhonghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3818-6b8a440aa644dc49b70f9b665532240854150051a0509c09aa8bb12c922283ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>mammals</topic><topic>pig</topic><topic>preimplantation embryonic development</topic><topic>single‐cell RNA‐seq</topic><topic>transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kong, Qingran</creatorcontrib><creatorcontrib>Yang, Xu</creatorcontrib><creatorcontrib>Zhang, Heng</creatorcontrib><creatorcontrib>Liu, Shichao</creatorcontrib><creatorcontrib>Zhao, Jianchao</creatorcontrib><creatorcontrib>Zhang, Jiaming</creatorcontrib><creatorcontrib>Weng, Xiaogang</creatorcontrib><creatorcontrib>Jin, Junxue</creatorcontrib><creatorcontrib>Liu, Zhonghua</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kong, Qingran</au><au>Yang, Xu</au><au>Zhang, Heng</au><au>Liu, Shichao</au><au>Zhao, Jianchao</au><au>Zhang, Jiaming</au><au>Weng, Xiaogang</au><au>Jin, Junxue</au><au>Liu, Zhonghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2020-01</date><risdate>2020</risdate><volume>34</volume><issue>1</issue><spage>691</spage><epage>705</epage><pages>691-705</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>The inner cell mass (ICM) in blastocyst is the origin of all somatic and germ cells in mammals and pluripotent stem cells (PSCs) in vitro. As the conserved principles between pig and human, here we performed comprehensive single‐cell RNA‐seq for porcine early embryos from oocyte to early blastocyst (EB). We show the specification of the ICM and trophectoderm in morula and the molecular signature of the precursors. We demonstrate the existence of naïve pluripotency signature in morula and ICM of EB, and the specific pluripotent genes and the activity of signalling pathways highlight the characteristics of the naïve pluripotency. We observe the absence of dosage compensation with respect to X‐chromosome (XC) in morula, and incomplete dosage compensation in the EB. However, the dynamics of dosage compensation may be independent of the expression of XIST induced XC inactivation. Our study describes molecular landmarks of embryogenesis in pig that will provide a better strategy for derivation of porcine PSCs and improve research in regenerative medicine.</abstract><cop>United States</cop><pmid>31914626</pmid><doi>10.1096/fj.201901818RR</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0892-6638
ispartof The FASEB journal, 2020-01, Vol.34 (1), p.691-705
issn 0892-6638
1530-6860
language eng
recordid cdi_proquest_miscellaneous_2335173802
source Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects mammals
pig
preimplantation embryonic development
single‐cell RNA‐seq
transcriptome
title Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T11%3A22%3A47IST&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=Lineage%20specification%20and%20pluripotency%20revealed%20by%20transcriptome%20analysis%20from%20oocyte%20to%20blastocyst%20in%20pig&rft.jtitle=The%20FASEB%20journal&rft.au=Kong,%20Qingran&rft.date=2020-01&rft.volume=34&rft.issue=1&rft.spage=691&rft.epage=705&rft.pages=691-705&rft.issn=0892-6638&rft.eissn=1530-6860&rft_id=info:doi/10.1096/fj.201901818RR&rft_dat=%3Cproquest_cross%3E2335173802%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2335173802&rft_id=info:pmid/31914626&rfr_iscdi=true