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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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Autores principales: Feng, Meiying, Dang, Nannan, Bai, Yinshan, Wei, Hengxi, Meng, Li, Wang, Kai, Zhao, Zhihong, Chen, Yun, Gao, Fenglei, Chen, Zhilin, Li, Li, Zhang, Shouquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297735/
https://www.ncbi.nlm.nih.gov/pubmed/30483791
http://dx.doi.org/10.3892/mmr.2018.9675
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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_facet 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 Feng, Meiying
collection PubMed
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.
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spelling pubmed-62977352018-12-26 Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity Feng, Meiying Dang, Nannan Bai, Yinshan Wei, Hengxi Meng, Li Wang, Kai Zhao, Zhihong Chen, Yun Gao, Fenglei Chen, Zhilin Li, Li Zhang, Shouquan Mol Med Rep Articles 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. D.A. Spandidos 2019-01 2018-11-20 /pmc/articles/PMC6297735/ /pubmed/30483791 http://dx.doi.org/10.3892/mmr.2018.9675 Text en Copyright: © Feng et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Feng, Meiying
Dang, Nannan
Bai, Yinshan
Wei, Hengxi
Meng, Li
Wang, Kai
Zhao, Zhihong
Chen, Yun
Gao, Fenglei
Chen, Zhilin
Li, Li
Zhang, Shouquan
Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
title Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
title_full Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
title_fullStr Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
title_full_unstemmed Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
title_short Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity
title_sort differential expression profiles of long non-coding rnas during the mouse pronuclear stage under normal gravity and simulated microgravity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297735/
https://www.ncbi.nlm.nih.gov/pubmed/30483791
http://dx.doi.org/10.3892/mmr.2018.9675
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