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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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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fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6297735</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A569755866</galeid><sourcerecordid>A569755866</sourcerecordid><originalsourceid>FETCH-LOGICAL-c482t-5d51132cbf4172ae9057a5d136fa35b448bd5b9737d0d4629d1370ef6beaf2a83</originalsourceid><addsrcrecordid>eNptUstqFTEYHkSxtbp0KwE3bs4xl0ky2QiHeoWiILoOmcmfaUomOSYzxe58ADe-ok9ihh6rFckiCd8l_F--pnlM8JZ1ij6fprylmHRbJSS_0xwTqciGYdzePZypUvKoeVDKBcaCU67uN0cMtx2r4HHz_aV3DjLE2ZuA4Os-Qyk-RbTPyfkABSWHQoojiin-_PZjSNbXy8f3u4LsktfzfA5oSkuBVROXIYDJqMxmBLREC7kq81TNx2wu_XyFTLSo-GkJZgaLJj_kdIAeNvecCQUeHfaT5vPrV59O327OPrx5d7o72wxtR-cNt5wQRofetURSAwpzabglTDjDeN-2XW95rySTFttWUFUhicGJHoyjpmMnzYtr3_3ST2CHOn02Qe-zn0y-0sl4fRuJ_lyP6VJXLykZrwbPDgY5fVmgzHryZYAQTISahKaEdYK1nKhKffoP9SItOdbxKktgoaon_8MaTQDto0v13WE11TsulOS8E6Kytv9h1WWhxpgirD92W7C5FtSMS8ngbmYkWK_10bU-eq2PXutT-U_-DuaG_bsv7BfLUMRu</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2160696295</pqid></control><display><type>article</type><title>Differential expression profiles of long non‑coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity</title><source>Spandidos Publications Journals</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><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</creator><creatorcontrib>Feng, Meiying ; Dang, Nannan ; Bai, Yinshan ; Wei, Hengxi ; Meng, Li ; Wang, Kai ; Zhao, Zhihong ; Chen, Yun ; Gao, Fenglei ; Chen, Zhilin ; Li, Li ; Zhang, Shouquan</creatorcontrib><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><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 & 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 & 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. Spandidos</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190101</creationdate><title>Differential expression profiles of long non‑coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity</title><author>Feng, Meiying ; Dang, Nannan ; Bai, Yinshan ; Wei, Hengxi ; Meng, Li ; Wang, Kai ; Zhao, Zhihong ; Chen, Yun ; Gao, Fenglei ; Chen, Zhilin ; Li, Li ; Zhang, Shouquan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-5d51132cbf4172ae9057a5d136fa35b448bd5b9737d0d4629d1370ef6beaf2a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Actinin</topic><topic>Animals</topic><topic>Binding sites</topic><topic>Cell adhesion & migration</topic><topic>Cell culture</topic><topic>Cell migration</topic><topic>Cortex</topic><topic>Cytoskeleton</topic><topic>Developmental stages</topic><topic>Embryogenesis</topic><topic>Embryonic development</topic><topic>Embryonic Development - genetics</topic><topic>Embryos</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation - genetics</topic><topic>Gene Ontology</topic><topic>Gene Regulatory Networks - genetics</topic><topic>Genetic aspects</topic><topic>Gravity</topic><topic>Health aspects</topic><topic>Investigations</topic><topic>Laboratory animals</topic><topic>Medical laboratories</topic><topic>Membrane proteins</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microgravity</topic><topic>Polymerase chain reaction</topic><topic>Pronucleus</topic><topic>Protein transport</topic><topic>Reverse transcription</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Signal transduction</topic><topic>Sperm</topic><topic>Tubulin</topic><topic>Weightlessness</topic><topic>Weightlessness Simulation - methods</topic><toplevel>online_resources</toplevel><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><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech 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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular medicine reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Meiying</au><au>Dang, Nannan</au><au>Bai, Yinshan</au><au>Wei, Hengxi</au><au>Meng, Li</au><au>Wang, Kai</au><au>Zhao, Zhihong</au><au>Chen, Yun</au><au>Gao, Fenglei</au><au>Chen, Zhilin</au><au>Li, Li</au><au>Zhang, Shouquan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression profiles of long non‑coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity</atitle><jtitle>Molecular medicine reports</jtitle><addtitle>Mol Med Rep</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>19</volume><issue>1</issue><spage>155</spage><epage>164</epage><pages>155-164</pages><issn>1791-2997</issn><eissn>1791-3004</eissn><abstract>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.</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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