• 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

Notch 和 Hippo 信号通路在草莓 Notch1(Sbno1)上汇聚,协同激活滋养层细胞特化过程中的 Cdx2。

Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm.

机构信息

Department of Developmental Neurobiology, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo, Aoba, Sendai, Miyagi 980-8575, Japan.

Department of Molecular Physiology, National Cerebral and Cardiovascular Center Research Institute, 5-7-1 Fujishiro-dai, Suita, Osaka, 565-8565, Japan.

出版信息

Sci Rep. 2017 Apr 12;7:46135. doi: 10.1038/srep46135.

DOI:10.1038/srep46135
PMID:28401892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5389439/
Abstract

The first binary cell fate decision occurs at the morula stage and gives rise to two distinct types of cells that constitute the trophectoderm (TE) and inner cell mass (ICM). The cell fate determinant, Cdx2, is induced in TE cells and plays an essential role in their differentiation and maintenance. Notch and Hippo signaling cascades are assumed to converge onto regulatory elements of Cdx2, however, the underlying molecular mechanisms are largely unknown. Here, we show involvement of Strawberry Notch1 (Sbno1), a novel chromatin factor of the helicase superfamily 2, during preimplantation development. Sbno1 knockout embryos die at the preimplantation stage without forming a blastocoel, and Cdx2 is not turned on even though both Yap and Tead4 reside normally in nuclei. Accordingly, Sbno1 acts on the trophectoderm-enhancer (TEE) of Cdx2, ensuring its robust and synergistic activation by the Yap/Tead4 and NICD/Rbpj complexes. Interestingly, this synergism is enhanced when cells are mechanically stretched, which might reflect that TE cells are continuously stretched by the expanding ICM and blastocoel cavity. In addition, the histone chaperone, FACT (FAcilitates Chromatin Transcription) physically interacts with Sbno1. Our data provide new evidence on TE specification, highlighting unexpected but essential functions of the highly conserved chromatin factor, Sbno1.

摘要

第一个二元细胞命运决定发生在桑葚胚阶段,产生两种不同类型的细胞,即滋养外胚层 (TE) 和内细胞团 (ICM)。细胞命运决定因子 Cdx2 在 TE 细胞中被诱导,并在其分化和维持中发挥重要作用。Notch 和 Hippo 信号级联被认为集中在 Cdx2 的调节元件上,然而,潜在的分子机制在很大程度上尚不清楚。在这里,我们展示了 Strawberry Notch1 (Sbno1) 在植入前胚胎发育中的参与,Sbno1 是解旋酶超家族 2 的一种新型染色质因子。Sbno1 敲除胚胎在植入前阶段死亡,没有形成囊胚腔,即使 Yap 和 Tead4 正常位于核内,Cdx2 也没有被激活。因此,Sbno1 作用于 Cdx2 的滋养外胚层增强子 (TEE),确保 Yap/Tead4 和 NICD/Rbpj 复合物对其进行强大的协同激活。有趣的是,当细胞受到机械拉伸时,这种协同作用会增强,这可能反映出 TE 细胞不断受到不断扩张的 ICM 和囊胚腔的拉伸。此外,组蛋白伴侣 FACT (促进染色质转录) 与 Sbno1 发生物理相互作用。我们的数据提供了 TE 特化的新证据,突出了高度保守的染色质因子 Sbno1 的意外但必不可少的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/20c7710eceac/srep46135-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/ac9e3aa0347d/srep46135-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/951bb4af154c/srep46135-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/d7b79932756e/srep46135-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/1d5038037b9a/srep46135-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/e8ecf85ef7f3/srep46135-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/3f57507f6e8d/srep46135-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/20c7710eceac/srep46135-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/ac9e3aa0347d/srep46135-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/951bb4af154c/srep46135-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/d7b79932756e/srep46135-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/1d5038037b9a/srep46135-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/e8ecf85ef7f3/srep46135-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/3f57507f6e8d/srep46135-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e3/5389439/20c7710eceac/srep46135-f7.jpg

相似文献

1
Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm.Notch 和 Hippo 信号通路在草莓 Notch1(Sbno1)上汇聚,协同激活滋养层细胞特化过程中的 Cdx2。
Sci Rep. 2017 Apr 12;7:46135. doi: 10.1038/srep46135.
2
Tead4 is required for specification of trophectoderm in pre-implantation mouse embryos.在植入前的小鼠胚胎中,滋养外胚层的特化需要Tead4。
Mech Dev. 2008 Mar-Apr;125(3-4):270-83. doi: 10.1016/j.mod.2007.11.002. Epub 2007 Nov 17.
3
The role of TEAD4 in trophectoderm commitment and development is not conserved in non-rodent mammals.TEAD4 在滋养层细胞特化和发育中的作用在非啮齿类哺乳动物中没有保守性。
Development. 2024 Oct 15;151(20). doi: 10.1242/dev.202993. Epub 2024 Sep 24.
4
The role of Cdx2 as a lineage specific transcriptional repressor for pluripotent network during the first developmental cell lineage segregation.Cdx2 在第一次细胞谱系分离过程中作为多能性网络的谱系特异性转录抑制因子的作用。
Sci Rep. 2017 Dec 7;7(1):17156. doi: 10.1038/s41598-017-16009-w.
5
The Necessity of OCT-4 and CDX2 for Early Development and Gene Expression Involved in Differentiation of Inner Cell Mass and Trophectoderm Lineages in Bovine Embryos.OCT-4和CDX2对牛胚胎内细胞团和滋养外胚层谱系分化中早期发育及基因表达的必要性
Cell Reprogram. 2016 Oct;18(5):309-318. doi: 10.1089/cell.2015.0081. Epub 2016 Aug 8.
6
Notch and hippo converge on Cdx2 to specify the trophectoderm lineage in the mouse blastocyst.Notch信号通路和Hippo信号通路共同作用于Cdx2,以确定小鼠囊胚中的滋养外胚层谱系。
Dev Cell. 2014 Aug 25;30(4):410-22. doi: 10.1016/j.devcel.2014.06.019. Epub 2014 Aug 7.
7
Roles of ERα during mouse trophectoderm lineage differentiation: revealed by antagonist and agonist of ERα.雌激素受体α(ERα)在小鼠滋养外胚层谱系分化中的作用:由ERα拮抗剂和激动剂揭示。
Dev Growth Differ. 2016 Apr;58(3):327-38. doi: 10.1111/dgd.12276. Epub 2016 Apr 1.
8
Maternal-zygotic knockout reveals a critical role of Cdx2 in the morula to blastocyst transition.母源-合子敲除揭示了Cdx2在桑椹胚向囊胚转变中的关键作用。
Dev Biol. 2015 Feb 15;398(2):147-52. doi: 10.1016/j.ydbio.2014.12.004. Epub 2014 Dec 13.
9
Mechanisms of trophectoderm fate specification in preimplantation mouse development.原肠胚滋养层命运特化的机制在小鼠植入前胚胎发育中的作用。
Dev Growth Differ. 2010 Apr;52(3):263-73. doi: 10.1111/j.1440-169X.2009.01158.x. Epub 2010 Jan 20.
10
Distinct mechanisms regulate Cdx2 expression in the blastocyst and in trophoblast stem cells.不同的机制调控着胚泡和滋养层干细胞中Cdx2的表达。
Sci Rep. 2016 Jun 3;6:27139. doi: 10.1038/srep27139.

引用本文的文献

1
Generative model for the first cell fate bifurcation in mammalian development.哺乳动物发育中首个细胞命运分支的生成模型。
Development. 2025 Aug 5. doi: 10.1242/dev.204717.
2
Strawberry notch 1 safeguards neuronal genome via regulation of Yeats4 expression.草莓缺口1通过调控Yeats4表达来保护神经元基因组。
Cell Death Discov. 2025 Jul 24;11(1):342. doi: 10.1038/s41420-025-02640-4.
3
The Notch pathway in Metazoa: a comparative analysis across cnidarians and beyond.后生动物中的Notch信号通路:刺胞动物及其他生物的比较分析

本文引用的文献

1
Asymmetric division of contractile domains couples cell positioning and fate specification.收缩域的不对称分裂将细胞定位与命运决定联系起来。
Nature. 2016 Aug 18;536(7616):344-348. doi: 10.1038/nature18958. Epub 2016 Aug 3.
2
Rho-associated protein kinase regulates subcellular localisation of Angiomotin and Hippo-signalling during preimplantation mouse embryo development.Rho相关蛋白激酶在小鼠植入前胚胎发育过程中调节血管动蛋白的亚细胞定位和河马信号通路。
Reprod Biomed Online. 2016 Sep;33(3):381-90. doi: 10.1016/j.rbmo.2016.06.028. Epub 2016 Jul 1.
3
Distinct mechanisms regulate Cdx2 expression in the blastocyst and in trophoblast stem cells.
Evodevo. 2025 Jun 14;16(1):8. doi: 10.1186/s13227-025-00246-6.
4
Generative model for the first cell fate bifurcation in mammalian development.哺乳动物发育中首个细胞命运分支的生成模型。
bioRxiv. 2025 Feb 25:2025.02.24.639895. doi: 10.1101/2025.02.24.639895.
5
Signaling pathway regulators in preimplantation embryos.植入前胚胎中的信号通路调节因子。
J Mol Histol. 2024 Dec 27;56(1):57. doi: 10.1007/s10735-024-10338-7.
6
Sbno1 mediates cell-cell communication between neural stem cells and microglia through small extracellular vesicles.Sbno1通过小细胞外囊泡介导神经干细胞与小胶质细胞之间的细胞间通讯。
Cell Biosci. 2024 Sep 29;14(1):125. doi: 10.1186/s13578-024-01296-4.
7
Extracellular vesicles-coupled miRNAs from oviduct and uterus modulate signaling pathways related to lipid metabolism and bovine early embryo development.来自输卵管和子宫的细胞外囊泡耦联的微小RNA调节与脂质代谢和牛早期胚胎发育相关的信号通路。
J Anim Sci Biotechnol. 2024 Apr 4;15(1):51. doi: 10.1186/s40104-024-01008-5.
8
How great thou ART: biomechanical properties of oocytes and embryos as indicators of quality in assisted reproductive technologies.《你真伟大》:卵母细胞和胚胎的生物力学特性作为辅助生殖技术中质量指标的研究
Front Cell Dev Biol. 2024 Feb 15;12:1342905. doi: 10.3389/fcell.2024.1342905. eCollection 2024.
9
YAP-mediated trophoblast dysfunction: the common pathway underlying pregnancy complications.YAP 介导的滋养层功能障碍:妊娠并发症的共同通路。
Cell Commun Signal. 2023 Dec 14;21(1):353. doi: 10.1186/s12964-023-01371-2.
10
Coordination of host and endosymbiont gene expression governs endosymbiont growth and elimination in the cereal weevil Sitophilus spp.宿主和内共生体基因表达的协调控制着谷物象鼻虫属中内共生体的生长和消除。
Microbiome. 2023 Dec 13;11(1):274. doi: 10.1186/s40168-023-01714-8.
不同的机制调控着胚泡和滋养层干细胞中Cdx2的表达。
Sci Rep. 2016 Jun 3;6:27139. doi: 10.1038/srep27139.
4
YAP Drives Growth by Controlling Transcriptional Pause Release from Dynamic Enhancers.YAP 通过控制动态增强子转录暂停释放来驱动生长。
Mol Cell. 2015 Oct 15;60(2):328-37. doi: 10.1016/j.molcel.2015.09.001. Epub 2015 Oct 1.
5
Mechanical Allostery: Evidence for a Force Requirement in the Proteolytic Activation of Notch.机械变构:Notch蛋白水解激活中力需求的证据
Dev Cell. 2015 Jun 22;33(6):729-36. doi: 10.1016/j.devcel.2015.05.004. Epub 2015 Jun 4.
6
TEAD and YAP regulate the enhancer network of human embryonic pancreatic progenitors.TEAD和YAP调控人类胚胎胰腺祖细胞的增强子网络。
Nat Cell Biol. 2015 May;17(5):615-626. doi: 10.1038/ncb3160. Epub 2015 Apr 27.
7
Transcription factor AP-2γ induces early Cdx2 expression and represses HIPPO signaling to specify the trophectoderm lineage.转录因子AP-2γ诱导早期Cdx2表达并抑制HIPPO信号通路以确定滋养外胚层谱系。
Development. 2015 May 1;142(9):1606-15. doi: 10.1242/dev.120238. Epub 2015 Apr 9.
8
Cellular energy stress induces AMPK-mediated regulation of YAP and the Hippo pathway.细胞能量应激诱导AMPK介导的YAP和Hippo信号通路调控。
Nat Cell Biol. 2015 Apr;17(4):500-10. doi: 10.1038/ncb3111. Epub 2015 Mar 9.
9
AMPK modulates Hippo pathway activity to regulate energy homeostasis.AMPK调节Hippo信号通路活性以调控能量稳态。
Nat Cell Biol. 2015 Apr;17(4):490-9. doi: 10.1038/ncb3113. Epub 2015 Mar 9.
10
Dual role of YAP and TAZ in renewal of the intestinal epithelium.YAP 和 TAZ 在肠道上皮更新中的双重作用。
Nat Cell Biol. 2015 Jan;17(1):7-19. doi: 10.1038/ncb3084. Epub 2014 Dec 22.