• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

- 基因敲除小鼠胚胎囊胚形成障碍。

Impaired Blastocyst Formation in -Knockdown Mouse Embryos.

机构信息

School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea.

Developmental Epigenetics Laboratory, Department of Animal Science, Michigan State University, East Lansing, MI 48824, USA.

出版信息

Int J Mol Sci. 2023 Jan 10;24(2):1385. doi: 10.3390/ijms24021385.

DOI:10.3390/ijms24021385
PMID:36674899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9867088/
Abstract

Ligand of Numb-protein X 2 (LNX2) is an E3 ubiquitin ligase that is known to regulate Notch signaling by participating in NUMB protein degradation. Notch signaling is important for differentiation and proliferation in mammals, and plays a significant role in blastocyst formation during early embryonic development. In this study, we investigated in mouse preimplantation embryos. Expression analysis showed that is expressed in oocytes and preimplantation embryos. -knockdown embryos normally progress to the morula stage, but the majority of them do not develop into normal blastocysts. Transcript analysis revealed that the expression levels of genes critical for cell lineage specification, including octamer-binding transcription factor 4 (), are increased in knockdown embryos. Furthermore, the expression levels of Notch and Hippo signaling-related genes are also increased by knockdown. Collectively, our results show that is important for blastocyst formation in mice, suggest that this may act via lineage specification of inner cell mass, and further show that may be involved in transcriptionally regulating various genes implicated in early embryonic development.

摘要

神经嵴衍生分泌因子 2 配体(LNX2)是一种 E3 泛素连接酶,已知通过参与 NUMB 蛋白降解来调节 Notch 信号通路。Notch 信号通路在哺乳动物的分化和增殖中起重要作用,并在早期胚胎发育中的囊胚形成中发挥重要作用。在这项研究中,我们研究了其在小鼠植入前胚胎中的作用。表达分析表明, 在卵母细胞和植入前胚胎中均有表达。 敲低胚胎正常发育到桑葚胚阶段,但大多数胚胎不能发育成正常的囊胚。转录分析显示,参与细胞谱系特化的关键基因,包括八聚体结合转录因子 4()的表达水平在 敲低胚胎中增加。此外,Notch 和 Hippo 信号通路相关基因的表达水平也因 敲低而增加。综上所述,我们的研究结果表明, 在小鼠囊胚形成中具有重要作用,提示其可能通过内细胞团的谱系特化起作用,进一步表明其可能参与转录调控与早期胚胎发育相关的各种基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/e2bf4af5907b/ijms-24-01385-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/cf37b5c91fa5/ijms-24-01385-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/b6b257ad32ec/ijms-24-01385-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/1212339eb1a0/ijms-24-01385-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/e2bf4af5907b/ijms-24-01385-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/cf37b5c91fa5/ijms-24-01385-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/b6b257ad32ec/ijms-24-01385-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/1212339eb1a0/ijms-24-01385-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9867088/e2bf4af5907b/ijms-24-01385-g004.jpg

相似文献

1
Impaired Blastocyst Formation in -Knockdown Mouse Embryos.- 基因敲除小鼠胚胎囊胚形成障碍。
Int J Mol Sci. 2023 Jan 10;24(2):1385. doi: 10.3390/ijms24021385.
2
NSUN5 is essential for proper cell proliferation and differentiation of mouse preimplantation embryos.NSUN5 对于小鼠胚胎植入前细胞的正常增殖和分化是必需的。
Reproduction. 2024 May 31;168(1). doi: 10.1530/REP-24-0079. Print 2024 Jul 1.
3
Identification of a novel embryo-prevalent gene, , involved in preimplantation embryogenesis in mice.鉴定一个新的胚胎期表达基因 , 参与小鼠植入前胚胎发生。
FASEB J. 2019 Oct;33(10):11326-11337. doi: 10.1096/fj.201900370RR. Epub 2019 Jul 19.
4
A tale of two cell-fates: role of the Hippo signaling pathway and transcription factors in early lineage formation in mouse preimplantation embryos.两个细胞命运的故事:Hippo 信号通路和转录因子在小鼠着床前胚胎早期谱系形成中的作用。
Mol Hum Reprod. 2020 Sep 1;26(9):653-664. doi: 10.1093/molehr/gaaa052.
5
Sox2 is essential for formation of trophectoderm in the preimplantation embryo.Sox2 对于胚胎着床前胚胎滋养外胚层的形成至关重要。
PLoS One. 2010 Nov 12;5(11):e13952. doi: 10.1371/journal.pone.0013952.
6
Knockdown of p66Shc Alters Lineage-Associated Transcription Factor Expression in Mouse Blastocysts.敲低 p66Shc 改变小鼠囊胚中与谱系相关的转录因子表达。
Stem Cells Dev. 2018 Nov 1;27(21):1479-1493. doi: 10.1089/scd.2018.0131. Epub 2018 Sep 6.
7
DDX21 is a p38-MAPK-sensitive nucleolar protein necessary for mouse preimplantation embryo development and cell-fate specification.DDX21 是一种 p38-MAPK 敏感的核仁蛋白,对于小鼠胚胎植入前发育和细胞命运特化是必需的。
Open Biol. 2021 Jul;11(7):210092. doi: 10.1098/rsob.210092. Epub 2021 Jul 14.
8
CHAF1b, chromatin assembly factor-1 subunit b, is essential for mouse preimplantation embryos.CHAF1b,染色质组装因子 1 亚基 b,对小鼠植入前胚胎是必需的。
Int J Biol Macromol. 2022 Jan 15;195:547-557. doi: 10.1016/j.ijbiomac.2021.11.181. Epub 2021 Dec 11.
9
Deubiquitylase ubiquitin-specific protease 7 plays a crucial role in the lineage differentiation of preimplantation blastocysts†.去泛素化酶泛素特异性蛋白酶 7 在胚胎植入前囊胚的谱系分化中起着至关重要的作用†。
Biol Reprod. 2024 Jul 12;111(1):28-42. doi: 10.1093/biolre/ioae034.
10
Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differences.CRISPR/Cas9 靶向敲除 POU5F1 后对小鼠和人类植入前胚胎发育的比较分析揭示了种间差异。
Hum Reprod. 2021 Apr 20;36(5):1242-1252. doi: 10.1093/humrep/deab027.

引用本文的文献

1
Functional Characterization and Heterogeneity Analysis of Ribosomal Proteins in Mouse Preimplantation Embryos.小鼠植入前胚胎中核糖体蛋白的功能表征与异质性分析
FASEB J. 2025 Jun 15;39(11):e70662. doi: 10.1096/fj.202500574RR.

本文引用的文献

1
Interplay Between Notch and YAP/TAZ Pathways in the Regulation of Cell Fate During Embryo Development.Notch与YAP/TAZ信号通路在胚胎发育过程中细胞命运调控中的相互作用
Front Cell Dev Biol. 2021 Aug 19;9:711531. doi: 10.3389/fcell.2021.711531. eCollection 2021.
2
Balanced Notch-Wnt signaling interplay is required for mouse embryo and fetal development.平衡的 Notch-Wnt 信号相互作用是小鼠胚胎和胎儿发育所必需的。
Reproduction. 2021 Apr;161(4):385-398. doi: 10.1530/REP-20-0435.
3
LNX1/LNX2 proteins: functions in neuronal signalling and beyond.
LNX1/LNX2蛋白:在神经元信号传导及其他方面的功能
Neuronal Signal. 2018 Jun 7;2(2):NS20170191. doi: 10.1042/NS20170191. eCollection 2018 Jun.
4
Light-induced injury in mouse embryos revealed by single-cell RNA sequencing.单细胞 RNA 测序揭示的小鼠胚胎光诱导损伤。
Biol Res. 2019 Aug 29;52(1):48. doi: 10.1186/s40659-019-0256-1.
5
Identification of a novel embryo-prevalent gene, , involved in preimplantation embryogenesis in mice.鉴定一个新的胚胎期表达基因 , 参与小鼠植入前胚胎发生。
FASEB J. 2019 Oct;33(10):11326-11337. doi: 10.1096/fj.201900370RR. Epub 2019 Jul 19.
6
The histone deacetylase HDAC1 positively regulates Notch signaling during wing development.组蛋白去乙酰化酶HDAC1在翅膀发育过程中正向调控Notch信号通路。
Biol Open. 2018 Feb 20;7(2):bio029637. doi: 10.1242/bio.029637.
7
Zeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination.Zeb2招募组蛋白去乙酰化酶-核小体重塑去乙酰化酶复合物(HDAC-NuRD)以抑制Notch信号,并控制雪旺细胞的分化和髓鞘再生。
Nat Neurosci. 2016 Aug;19(8):1060-72. doi: 10.1038/nn.4322. Epub 2016 Jun 13.
8
Lnx2 ubiquitin ligase is essential for exocrine cell differentiation in the early zebrafish pancreas.Lnx2泛素连接酶对于斑马鱼早期胰腺外分泌细胞的分化至关重要。
Proc Natl Acad Sci U S A. 2015 Oct 6;112(40):12426-31. doi: 10.1073/pnas.1517033112. Epub 2015 Sep 21.
9
Ubiquitin E3 Ligase LNX2 is Critical for Osteoclastogenesis In Vitro by Regulating M-CSF/RANKL Signaling and Notch2.泛素E3连接酶LNX2通过调节M-CSF/RANKL信号通路和Notch2对体外破骨细胞生成至关重要。
Calcif Tissue Int. 2015 May;96(5):465-75. doi: 10.1007/s00223-015-9967-7. Epub 2015 Feb 25.
10
Gli3 repressor controls cell fates and cell adhesion for proper establishment of neurogenic niche.Gli3阻遏物通过控制细胞命运和细胞黏附来正确建立神经发生微环境。
Cell Rep. 2014 Aug 21;8(4):1093-104. doi: 10.1016/j.celrep.2014.07.006. Epub 2014 Aug 7.