• 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

小鼠的前部模式形成

Anterior patterning in mouse.

作者信息

Beddington R S, Robertson E J

机构信息

Division of Mammalian Development, MRC National Institute for Medical Research, Ridgeway, Mill Hill, London, UK.

出版信息

Trends Genet. 1998 Jul;14(7):277-84. doi: 10.1016/s0168-9525(98)01499-1.

DOI:10.1016/s0168-9525(98)01499-1
PMID:9676530
Abstract

The anteroposterior axis of the vertebrate embryo becomes explicit during gastrulation, the process that converts a relatively featureless embryonic precursor population into new tissues assembled into a recognisable body pattern. Vertebrate embryos arrive at gastrulation in very different states in terms of their size, cell number and reliance on factors inherited from the unfertilized egg. However, they emerge from gastrulation looking very similar, and there is now extensive molecular genetic evidence to indicate that the bare essentials of the gastrulation process have been well conserved during evolution. Here, we review recent findings in the mouse that suggest that anterior identity is, in fact, established before gastrulation starts. They suggest that it is first manifest in extraembryonic tissue and that this tissue is essential for the embryo to develop normal anterior structures, such as the forebrain. We also argue that this precocious anterior pattern could have a counterpart in other non-mammalian vertebrates.

摘要

脊椎动物胚胎的前后轴在原肠胚形成过程中变得明确,原肠胚形成过程将相对无特征的胚胎前体细胞群转化为组装成可识别身体模式的新组织。脊椎动物胚胎在进入原肠胚形成阶段时,在大小、细胞数量以及对未受精卵中遗传因素的依赖程度方面处于非常不同的状态。然而,它们从原肠胚形成阶段出现时看起来非常相似,现在有大量分子遗传学证据表明,原肠胚形成过程的基本要素在进化过程中得到了很好的保留。在这里,我们回顾了小鼠最近的研究发现,这些发现表明,事实上,前部特征在原肠胚形成开始之前就已确立。它们表明,前部特征首先在胚外组织中显现,并且该组织对于胚胎发育正常的前部结构(如前脑)至关重要。我们还认为,这种早熟的前部模式可能在其他非哺乳动物脊椎动物中也有对应物。

相似文献

1
Anterior patterning in mouse.小鼠的前部模式形成
Trends Genet. 1998 Jul;14(7):277-84. doi: 10.1016/s0168-9525(98)01499-1.
2
Antero-posterior ectoderm patterning by canonical Wnt signaling during ascidian development.在海鞘发育过程中,经典 Wnt 信号对前后外胚层的模式形成。
PLoS Genet. 2019 Mar 29;15(3):e1008054. doi: 10.1371/journal.pgen.1008054. eCollection 2019 Mar.
3
Mouse gastrulation: the formation of a mammalian body plan.小鼠原肠胚形成:哺乳动物身体蓝图的形成。
Mech Dev. 1997 Nov;68(1-2):3-25. doi: 10.1016/s0925-4773(97)00123-8.
4
Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo.前原始内胚层可能负责小鼠胚胎中前神经板的模式形成。
Curr Biol. 1996 Nov 1;6(11):1487-96. doi: 10.1016/s0960-9822(96)00753-1.
5
Anterior identity is established in chick epiblast by hypoblast and anterior definitive endoderm.下胚层和前确定内胚层在鸡胚外胚层中建立了前部特征。
Development. 2003 Nov;130(21):5091-101. doi: 10.1242/dev.00712. Epub 2003 Aug 27.
6
The genome-wide molecular regulation of mouse gastrulation embryo.小鼠原肠胚形成过程中的全基因组分子调控
Sci China Life Sci. 2017 Apr;60(4):363-369. doi: 10.1007/s11427-016-0285-3. Epub 2017 Feb 27.
7
Requirement for Wnt3 in vertebrate axis formation.脊椎动物轴形成过程中对Wnt3的需求。
Nat Genet. 1999 Aug;22(4):361-5. doi: 10.1038/11932.
8
Ras-dva, a member of novel family of small GTPases, is required for the anterior ectoderm patterning in the Xenopus laevis embryo.Ras-dva是小GTP酶新家族的成员,在非洲爪蟾胚胎的前外胚层模式形成中是必需的。
Development. 2006 Feb;133(3):485-94. doi: 10.1242/dev.02207.
9
A conserved role for non-neural ectoderm cells in early neural development.非神经外胚层细胞在早期神经发育中的保守作用。
Development. 2014 Nov;141(21):4127-38. doi: 10.1242/dev.107425. Epub 2014 Oct 1.
10
Control of early anterior-posterior patterning in the mouse embryo by TGF-beta signalling.转化生长因子-β信号通路对小鼠胚胎早期前后模式的调控
Philos Trans R Soc Lond B Biol Sci. 2003 Aug 29;358(1436):1351-7; discussion 1357. doi: 10.1098/rstb.2003.1332.

引用本文的文献

1
Trans-scale live-imaging of an E5.5 mouse embryo using incubator-type biaxial light-sheet microscopy.使用培养箱型双轴光片显微镜对E5.5小鼠胚胎进行跨尺度实时成像。
Life Sci Alliance. 2025 Jan 15;8(3). doi: 10.26508/lsa.202402839. Print 2025 Mar.
2
Capture of Mouse and Human Stem Cells with Features of Formative Pluripotency.捕获具有形成多潜能性特征的小鼠和人类干细胞。
Cell Stem Cell. 2021 Mar 4;28(3):453-471.e8. doi: 10.1016/j.stem.2020.11.005. Epub 2020 Dec 2.
3
Loss of Cubilin, the intrinsic factor-vitamin B12 receptor, impairs visceral endoderm endocytosis and endodermal patterning in the mouse.
内因子-维生素 B12 受体 Cubilin 的缺失会损害小鼠内脏内胚层的胞吞作用和内胚层的模式形成。
Sci Rep. 2019 Jul 15;9(1):10168. doi: 10.1038/s41598-019-46559-0.
4
On the nature and function of organizers.论组织者的性质与功能。
Development. 2018 Mar 9;145(5):dev159525. doi: 10.1242/dev.159525.
5
Both Nodal signalling and stochasticity select for prospective distal visceral endoderm in mouse embryos.节点信号和随机性都选择了小鼠胚胎中未来的远端内脏内胚层。
Nat Commun. 2017 Nov 14;8(1):1492. doi: 10.1038/s41467-017-01625-x.
6
Wnt/ß-catenin signalling and the dynamics of fate decisions in early mouse embryos and embryonic stem (ES) cells.Wnt/β-连环蛋白信号传导与小鼠早期胚胎和胚胎干细胞(ES细胞)中命运决定的动态变化
Semin Cell Dev Biol. 2015 Dec;47-48:101-9. doi: 10.1016/j.semcdb.2015.08.011. Epub 2015 Aug 29.
7
Extra-embryonic Wnt3 regulates the establishment of the primitive streak in mice.胚胎外Wnt3调节小鼠原条的形成。
Dev Biol. 2015 Jul 1;403(1):80-8. doi: 10.1016/j.ydbio.2015.04.008. Epub 2015 Apr 20.
8
Single cell transcriptome amplification with MALBAC.利用MALBAC进行单细胞转录组扩增。
PLoS One. 2015 Mar 30;10(3):e0120889. doi: 10.1371/journal.pone.0120889. eCollection 2015.
9
Computational modeling reveals that a combination of chemotaxis and differential adhesion leads to robust cell sorting during tissue patterning.计算模型表明,趋化作用和差异黏附的结合导致组织图案形成过程中强大的细胞分选。
PLoS One. 2014 Oct 10;9(10):e109286. doi: 10.1371/journal.pone.0109286. eCollection 2014.
10
An interplay between extracellular signalling and the dynamics of the exit from pluripotency drives cell fate decisions in mouse ES cells.细胞外信号的相互作用和退出多能性的动力学驱动了小鼠胚胎干细胞的细胞命运决定。
Biol Open. 2014 Jun 20;3(7):614-26. doi: 10.1242/bio.20148409.