LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A

The study of preimplantation development is of great significance to reproductive biology and regenerative medicine. With the development of high-throughput deep sequencing technology, it has been found that lncRNAs play a very important role in the regulation of embryonic development. In this study...

Full description

Bibliographic Details
Main Authors: Daoyu Zhang, Yongfeng Zhou, Rong Huang, Yanhui Zhai, Di Wu, Xinglan An, Sheng Zhang, Lijing Shi, Qi Li, Xiangjie Kong, Hao Yu, Ziyi Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2022.971965/full
_version_ 1811261742201700352
author Daoyu Zhang
Yongfeng Zhou
Rong Huang
Yanhui Zhai
Di Wu
Xinglan An
Sheng Zhang
Lijing Shi
Qi Li
Xiangjie Kong
Hao Yu
Ziyi Li
author_facet Daoyu Zhang
Yongfeng Zhou
Rong Huang
Yanhui Zhai
Di Wu
Xinglan An
Sheng Zhang
Lijing Shi
Qi Li
Xiangjie Kong
Hao Yu
Ziyi Li
author_sort Daoyu Zhang
collection DOAJ
description The study of preimplantation development is of great significance to reproductive biology and regenerative medicine. With the development of high-throughput deep sequencing technology, it has been found that lncRNAs play a very important role in the regulation of embryonic development. In this study, key lncRNAs that regulate embryonic development were screened by analyzing the expression pattern of lncRNAs in porcine in vivo fertilization (IVV) embryos. By knocking down lncRNA expression in in vitro fertilization (IVF) embryos, we investigated its function and mechanism of regulating embryonic development. The results showed that the expression pattern of lncRNA was consistent with the time of gene activation. The lncRNAs were highly expressed in the 4-cell to blastocyst stage but barely expressed in the oocytes and 2-cell stage. So we speculated this part of lncRNAs may regulate gene expression. The lncRNA LOC102165808 (named lncT because the gene near this lncRNA is TFAP2C) was one of them. The knockdown (KD) of lncT inhibited embryonic development, resulting in decreased H3K4me3, H3K4me2, and H3K9me3, and increased DNA methylation. Meanwhile, RNAseq showed SIN3A was the top decreased gene in lncT-KD embryos. There was a severe blastocyst formation defect in SIN3A-KD embryos. Both lncT and SIN3A could affect NANOG and induce more cell apoptosis. In conclusion, the knockdown of lncT inhibits embryonic development by regulating H3K4me3, H3K4me2, DNA methylation, pluripotency gene, and apoptosis, and SIN3A is one of the downstream genes of lncT in regulating embryonic development.
first_indexed 2024-04-12T19:11:19Z
format Article
id doaj.art-87e1b4377f504b37affba6a51507e647
institution Directory Open Access Journal
issn 1664-042X
language English
last_indexed 2024-04-12T19:11:19Z
publishDate 2022-09-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Physiology
spelling doaj.art-87e1b4377f504b37affba6a51507e6472022-12-22T03:19:53ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2022-09-011310.3389/fphys.2022.971965971965LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3ADaoyu Zhang0Yongfeng Zhou1Rong Huang2Yanhui Zhai3Di Wu4Xinglan An5Sheng Zhang6Lijing Shi7Qi Li8Xiangjie Kong9Hao Yu10Ziyi Li11Key Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaDepartment of Emergency Medicine, First Hospital, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaCollege of Animal Science, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaCollege of Animal Science, Jilin University, Changchun, ChinaKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, First Hospital, Jilin University, Changchun, ChinaThe study of preimplantation development is of great significance to reproductive biology and regenerative medicine. With the development of high-throughput deep sequencing technology, it has been found that lncRNAs play a very important role in the regulation of embryonic development. In this study, key lncRNAs that regulate embryonic development were screened by analyzing the expression pattern of lncRNAs in porcine in vivo fertilization (IVV) embryos. By knocking down lncRNA expression in in vitro fertilization (IVF) embryos, we investigated its function and mechanism of regulating embryonic development. The results showed that the expression pattern of lncRNA was consistent with the time of gene activation. The lncRNAs were highly expressed in the 4-cell to blastocyst stage but barely expressed in the oocytes and 2-cell stage. So we speculated this part of lncRNAs may regulate gene expression. The lncRNA LOC102165808 (named lncT because the gene near this lncRNA is TFAP2C) was one of them. The knockdown (KD) of lncT inhibited embryonic development, resulting in decreased H3K4me3, H3K4me2, and H3K9me3, and increased DNA methylation. Meanwhile, RNAseq showed SIN3A was the top decreased gene in lncT-KD embryos. There was a severe blastocyst formation defect in SIN3A-KD embryos. Both lncT and SIN3A could affect NANOG and induce more cell apoptosis. In conclusion, the knockdown of lncT inhibits embryonic development by regulating H3K4me3, H3K4me2, DNA methylation, pluripotency gene, and apoptosis, and SIN3A is one of the downstream genes of lncT in regulating embryonic development.https://www.frontiersin.org/articles/10.3389/fphys.2022.971965/fulllncRNAshistone modificationDNA methylationSIN3Aporcine embryonic development
spellingShingle Daoyu Zhang
Yongfeng Zhou
Rong Huang
Yanhui Zhai
Di Wu
Xinglan An
Sheng Zhang
Lijing Shi
Qi Li
Xiangjie Kong
Hao Yu
Ziyi Li
LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A
Frontiers in Physiology
lncRNAs
histone modification
DNA methylation
SIN3A
porcine embryonic development
title LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A
title_full LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A
title_fullStr LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A
title_full_unstemmed LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A
title_short LncRNA affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene SIN3A
title_sort lncrna affects epigenetic reprogramming of porcine embryo development by regulating global epigenetic modification and the downstream gene sin3a
topic lncRNAs
histone modification
DNA methylation
SIN3A
porcine embryonic development
url https://www.frontiersin.org/articles/10.3389/fphys.2022.971965/full
work_keys_str_mv AT daoyuzhang lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT yongfengzhou lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT ronghuang lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT yanhuizhai lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT diwu lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT xinglanan lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT shengzhang lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT lijingshi lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT qili lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT xiangjiekong lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT haoyu lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a
AT ziyili lncrnaaffectsepigeneticreprogrammingofporcineembryodevelopmentbyregulatingglobalepigeneticmodificationandthedownstreamgenesin3a