Differential expression profiles of long non‑coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity

Pronuclear migration, which is the initial stage of embryonic development and the marker of zygote formation, is a crucial process during mammalian preimplantation embryonic development. Recent studies have revealed that long non‑coding RNAs (lncRNAs) serve an important role in early embryonic devel...

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Veröffentlicht in:Molecular medicine reports 2019-01, Vol.19 (1), p.155-164
Hauptverfasser: Feng, Meiying, Dang, Nannan, Bai, Yinshan, Wei, Hengxi, Meng, Li, Wang, Kai, Zhao, Zhihong, Chen, Yun, Gao, Fenglei, Chen, Zhilin, Li, Li, Zhang, Shouquan
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container_end_page 164
container_issue 1
container_start_page 155
container_title Molecular medicine reports
container_volume 19
creator Feng, Meiying
Dang, Nannan
Bai, Yinshan
Wei, Hengxi
Meng, Li
Wang, Kai
Zhao, Zhihong
Chen, Yun
Gao, Fenglei
Chen, Zhilin
Li, Li
Zhang, Shouquan
description Pronuclear migration, which is the initial stage of embryonic development and the marker of zygote formation, is a crucial process during mammalian preimplantation embryonic development. Recent studies have revealed that long non‑coding RNAs (lncRNAs) serve an important role in early embryonic development. However, the functional regulation of lncRNAs in this process has yet to be elucidated, largely due to the difficulty of assessing gene expression alterations during the very short time in which pronuclear migration occurs. It has previously been reported that migration of the pronucleus of a zygote can be obstructed by simulated microgravity. To investigate pronuclear migration in mice, a rotary cell culture system was employed, which generates simulated microgravity, in order to interfere with murine pronuclear migration. Subsequently, lncRNA sequencing was performed to investigate the mechanism underlying this process. In the present study, a comprehensive analysis of lncRNA profile during the mouse pronuclear stage was conducted, in which 3,307 lncRNAs were identified based on single‑cell RNA sequencing data. Furthermore, 52 lncRNAs were identified that were significantly differentially expressed. Subsequently, 10 lncRNAs were selected for validation by reverse transcription‑quantitative polymerase chain reaction, in which the same relative expression pattern was observed. The results revealed that 12 lncRNAs (lnc006745, lnc007956, lnc013100, lnc013782, lnc017097, lnc019869, lnc025838, lnc027046, lnc005454, lnc007956, lnc019410 and lnc019607), with tubulin β 4B class IVb or actinin α 4 as target genes, may be associated with the expression of microtubule and microfilament proteins. Binding association was confirmed using a dual‑luciferase reporter assay. Finally, Gene Ontology analysis revealed that the target genes of the differentially expressed lncRNAs participated in cellular processes associated with protein transport, binding, catalytic activity, membrane‑bounded organelle, protein complex and the cortical cytoskeleton. These findings suggested that these lncRNAs may be associated with migration of the mouse pronucleus.
doi_str_mv 10.3892/mmr.2018.9675
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Recent studies have revealed that long non‑coding RNAs (lncRNAs) serve an important role in early embryonic development. However, the functional regulation of lncRNAs in this process has yet to be elucidated, largely due to the difficulty of assessing gene expression alterations during the very short time in which pronuclear migration occurs. It has previously been reported that migration of the pronucleus of a zygote can be obstructed by simulated microgravity. To investigate pronuclear migration in mice, a rotary cell culture system was employed, which generates simulated microgravity, in order to interfere with murine pronuclear migration. Subsequently, lncRNA sequencing was performed to investigate the mechanism underlying this process. In the present study, a comprehensive analysis of lncRNA profile during the mouse pronuclear stage was conducted, in which 3,307 lncRNAs were identified based on single‑cell RNA sequencing data. Furthermore, 52 lncRNAs were identified that were significantly differentially expressed. Subsequently, 10 lncRNAs were selected for validation by reverse transcription‑quantitative polymerase chain reaction, in which the same relative expression pattern was observed. The results revealed that 12 lncRNAs (lnc006745, lnc007956, lnc013100, lnc013782, lnc017097, lnc019869, lnc025838, lnc027046, lnc005454, lnc007956, lnc019410 and lnc019607), with tubulin β 4B class IVb or actinin α 4 as target genes, may be associated with the expression of microtubule and microfilament proteins. Binding association was confirmed using a dual‑luciferase reporter assay. Finally, Gene Ontology analysis revealed that the target genes of the differentially expressed lncRNAs participated in cellular processes associated with protein transport, binding, catalytic activity, membrane‑bounded organelle, protein complex and the cortical cytoskeleton. These findings suggested that these lncRNAs may be associated with migration of the mouse pronucleus.</description><identifier>ISSN: 1791-2997</identifier><identifier>EISSN: 1791-3004</identifier><identifier>DOI: 10.3892/mmr.2018.9675</identifier><identifier>PMID: 30483791</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Actinin ; Animals ; Binding sites ; Cell adhesion &amp; migration ; Cell culture ; Cell migration ; Cortex ; Cytoskeleton ; Developmental stages ; Embryogenesis ; Embryonic development ; Embryonic Development - genetics ; Embryos ; Female ; Gene expression ; Gene Expression Profiling - methods ; Gene Expression Regulation - genetics ; Gene Ontology ; Gene Regulatory Networks - genetics ; Genetic aspects ; Gravity ; Health aspects ; Investigations ; Laboratory animals ; Medical laboratories ; Membrane proteins ; Mice ; Mice, Inbred C57BL ; Microgravity ; Polymerase chain reaction ; Pronucleus ; Protein transport ; Reverse transcription ; Ribonucleic acid ; RNA ; RNA, Long Noncoding - genetics ; Signal transduction ; Sperm ; Tubulin ; Weightlessness ; Weightlessness Simulation - methods</subject><ispartof>Molecular medicine reports, 2019-01, Vol.19 (1), p.155-164</ispartof><rights>COPYRIGHT 2019 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2019</rights><rights>Copyright: © Feng et al. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-5d51132cbf4172ae9057a5d136fa35b448bd5b9737d0d4629d1370ef6beaf2a83</citedby><cites>FETCH-LOGICAL-c482t-5d51132cbf4172ae9057a5d136fa35b448bd5b9737d0d4629d1370ef6beaf2a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30483791$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Meiying</creatorcontrib><creatorcontrib>Dang, Nannan</creatorcontrib><creatorcontrib>Bai, Yinshan</creatorcontrib><creatorcontrib>Wei, Hengxi</creatorcontrib><creatorcontrib>Meng, Li</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Zhao, Zhihong</creatorcontrib><creatorcontrib>Chen, Yun</creatorcontrib><creatorcontrib>Gao, Fenglei</creatorcontrib><creatorcontrib>Chen, Zhilin</creatorcontrib><creatorcontrib>Li, Li</creatorcontrib><creatorcontrib>Zhang, Shouquan</creatorcontrib><title>Differential expression profiles of long non‑coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity</title><title>Molecular medicine reports</title><addtitle>Mol Med Rep</addtitle><description>Pronuclear migration, which is the initial stage of embryonic development and the marker of zygote formation, is a crucial process during mammalian preimplantation embryonic development. Recent studies have revealed that long non‑coding RNAs (lncRNAs) serve an important role in early embryonic development. However, the functional regulation of lncRNAs in this process has yet to be elucidated, largely due to the difficulty of assessing gene expression alterations during the very short time in which pronuclear migration occurs. It has previously been reported that migration of the pronucleus of a zygote can be obstructed by simulated microgravity. To investigate pronuclear migration in mice, a rotary cell culture system was employed, which generates simulated microgravity, in order to interfere with murine pronuclear migration. Subsequently, lncRNA sequencing was performed to investigate the mechanism underlying this process. In the present study, a comprehensive analysis of lncRNA profile during the mouse pronuclear stage was conducted, in which 3,307 lncRNAs were identified based on single‑cell RNA sequencing data. Furthermore, 52 lncRNAs were identified that were significantly differentially expressed. Subsequently, 10 lncRNAs were selected for validation by reverse transcription‑quantitative polymerase chain reaction, in which the same relative expression pattern was observed. The results revealed that 12 lncRNAs (lnc006745, lnc007956, lnc013100, lnc013782, lnc017097, lnc019869, lnc025838, lnc027046, lnc005454, lnc007956, lnc019410 and lnc019607), with tubulin β 4B class IVb or actinin α 4 as target genes, may be associated with the expression of microtubule and microfilament proteins. Binding association was confirmed using a dual‑luciferase reporter assay. Finally, Gene Ontology analysis revealed that the target genes of the differentially expressed lncRNAs participated in cellular processes associated with protein transport, binding, catalytic activity, membrane‑bounded organelle, protein complex and the cortical cytoskeleton. These findings suggested that these lncRNAs may be associated with migration of the mouse pronucleus.</description><subject>Actinin</subject><subject>Animals</subject><subject>Binding sites</subject><subject>Cell adhesion &amp; migration</subject><subject>Cell culture</subject><subject>Cell migration</subject><subject>Cortex</subject><subject>Cytoskeleton</subject><subject>Developmental stages</subject><subject>Embryogenesis</subject><subject>Embryonic development</subject><subject>Embryonic Development - genetics</subject><subject>Embryos</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation - genetics</subject><subject>Gene Ontology</subject><subject>Gene Regulatory Networks - genetics</subject><subject>Genetic aspects</subject><subject>Gravity</subject><subject>Health aspects</subject><subject>Investigations</subject><subject>Laboratory animals</subject><subject>Medical laboratories</subject><subject>Membrane proteins</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microgravity</subject><subject>Polymerase chain reaction</subject><subject>Pronucleus</subject><subject>Protein transport</subject><subject>Reverse transcription</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Signal transduction</subject><subject>Sperm</subject><subject>Tubulin</subject><subject>Weightlessness</subject><subject>Weightlessness Simulation - methods</subject><issn>1791-2997</issn><issn>1791-3004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptUstqFTEYHkSxtbp0KwE3bs4xl0ky2QiHeoWiILoOmcmfaUomOSYzxe58ADe-ok9ihh6rFckiCd8l_F--pnlM8JZ1ij6fprylmHRbJSS_0xwTqciGYdzePZypUvKoeVDKBcaCU67uN0cMtx2r4HHz_aV3DjLE2ZuA4Os-Qyk-RbTPyfkABSWHQoojiin-_PZjSNbXy8f3u4LsktfzfA5oSkuBVROXIYDJqMxmBLREC7kq81TNx2wu_XyFTLSo-GkJZgaLJj_kdIAeNvecCQUeHfaT5vPrV59O327OPrx5d7o72wxtR-cNt5wQRofetURSAwpzabglTDjDeN-2XW95rySTFttWUFUhicGJHoyjpmMnzYtr3_3ST2CHOn02Qe-zn0y-0sl4fRuJ_lyP6VJXLykZrwbPDgY5fVmgzHryZYAQTISahKaEdYK1nKhKffoP9SItOdbxKktgoaon_8MaTQDto0v13WE11TsulOS8E6Kytv9h1WWhxpgirD92W7C5FtSMS8ngbmYkWK_10bU-eq2PXutT-U_-DuaG_bsv7BfLUMRu</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Feng, Meiying</creator><creator>Dang, Nannan</creator><creator>Bai, Yinshan</creator><creator>Wei, Hengxi</creator><creator>Meng, Li</creator><creator>Wang, Kai</creator><creator>Zhao, Zhihong</creator><creator>Chen, Yun</creator><creator>Gao, Fenglei</creator><creator>Chen, Zhilin</creator><creator>Li, Li</creator><creator>Zhang, Shouquan</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. 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Recent studies have revealed that long non‑coding RNAs (lncRNAs) serve an important role in early embryonic development. However, the functional regulation of lncRNAs in this process has yet to be elucidated, largely due to the difficulty of assessing gene expression alterations during the very short time in which pronuclear migration occurs. It has previously been reported that migration of the pronucleus of a zygote can be obstructed by simulated microgravity. To investigate pronuclear migration in mice, a rotary cell culture system was employed, which generates simulated microgravity, in order to interfere with murine pronuclear migration. Subsequently, lncRNA sequencing was performed to investigate the mechanism underlying this process. In the present study, a comprehensive analysis of lncRNA profile during the mouse pronuclear stage was conducted, in which 3,307 lncRNAs were identified based on single‑cell RNA sequencing data. Furthermore, 52 lncRNAs were identified that were significantly differentially expressed. Subsequently, 10 lncRNAs were selected for validation by reverse transcription‑quantitative polymerase chain reaction, in which the same relative expression pattern was observed. The results revealed that 12 lncRNAs (lnc006745, lnc007956, lnc013100, lnc013782, lnc017097, lnc019869, lnc025838, lnc027046, lnc005454, lnc007956, lnc019410 and lnc019607), with tubulin β 4B class IVb or actinin α 4 as target genes, may be associated with the expression of microtubule and microfilament proteins. Binding association was confirmed using a dual‑luciferase reporter assay. Finally, Gene Ontology analysis revealed that the target genes of the differentially expressed lncRNAs participated in cellular processes associated with protein transport, binding, catalytic activity, membrane‑bounded organelle, protein complex and the cortical cytoskeleton. These findings suggested that these lncRNAs may be associated with migration of the mouse pronucleus.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>30483791</pmid><doi>10.3892/mmr.2018.9675</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Actinin
Animals
Binding sites
Cell adhesion & migration
Cell culture
Cell migration
Cortex
Cytoskeleton
Developmental stages
Embryogenesis
Embryonic development
Embryonic Development - genetics
Embryos
Female
Gene expression
Gene Expression Profiling - methods
Gene Expression Regulation - genetics
Gene Ontology
Gene Regulatory Networks - genetics
Genetic aspects
Gravity
Health aspects
Investigations
Laboratory animals
Medical laboratories
Membrane proteins
Mice
Mice, Inbred C57BL
Microgravity
Polymerase chain reaction
Pronucleus
Protein transport
Reverse transcription
Ribonucleic acid
RNA
RNA, Long Noncoding - genetics
Signal transduction
Sperm
Tubulin
Weightlessness
Weightlessness Simulation - methods
title Differential expression profiles of long non‑coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
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