• 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

相似文献

1
The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.多效性小鼠表型多指斑点是由翻译起始因子 Eif3c 突变引起的,与 sonic hedgehog 信号通路的破坏有关。
FASEB J. 2011 May;25(5):1596-605. doi: 10.1096/fj.10-169771. Epub 2011 Feb 3.
2
Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice.Gli3 杂合功能缺失导致的桡侧多趾畸形可被小鼠 Zic3 功能丧失所挽救。
Hum Mol Genet. 2012 Apr 15;21(8):1888-96. doi: 10.1093/hmg/dds002. Epub 2012 Jan 10.
3
Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development.Gli3在小鼠肢体发育中对音猬因子进行基因调控的证据。
Mech Dev. 1997 Mar;62(2):175-82. doi: 10.1016/s0925-4773(97)00656-4.
4
Polydactyly in the mouse mutant Doublefoot involves altered Gli3 processing and is caused by a large deletion in cis to Indian hedgehog.小鼠突变体“双足”中的多指畸形涉及Gli3加工过程的改变,并且是由印度刺猬基因顺式方向的大片段缺失引起的。
Mech Dev. 2008 May-Jun;125(5-6):517-26. doi: 10.1016/j.mod.2008.01.001. Epub 2008 Jan 11.
5
Gata6-Dependent GLI3 Repressor Function is Essential in Anterior Limb Progenitor Cells for Proper Limb Development.在肢体前体细胞中,依赖Gata6的GLI3阻遏物功能对于正常肢体发育至关重要。
PLoS Genet. 2016 Jun 28;12(6):e1006138. doi: 10.1371/journal.pgen.1006138. eCollection 2016 Jun.
6
Expression of SHH signaling pathway components in the developing human lung.SHH 信号通路成分在人肺发育中的表达。
Histochem Cell Biol. 2010 Oct;134(4):327-35. doi: 10.1007/s00418-010-0738-2. Epub 2010 Sep 7.
7
Mutational Screening of GLI3, SHH, and SHH ZRS in 78 Chinese Children with Nonsyndromic Polydactyly.78例中国非综合征性多指(趾)畸形患儿的GLI3、SHH及SHH ZRS基因的突变筛查
Genet Test Mol Biomarkers. 2018 Sep;22(9):577-581. doi: 10.1089/gtmb.2018.0096.
8
Sonic hedgehog expression and its role in form-deprivation myopia in mice.音猬因子在小鼠形觉剥夺性近视中的表达及其作用
Curr Eye Res. 2009 Aug;34(8):623-35. doi: 10.1080/02713680903003492.
9
Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly.对102名中国非综合征性多指(趾)畸形儿童的GLI3、SHH、前ZRS和ZRS进行突变筛查。
Dev Dyn. 2017 May;246(5):392-402. doi: 10.1002/dvdy.24488. Epub 2017 Feb 27.
10
Mouse limbs expressing only the Gli3 repressor resemble those of Sonic hedgehog mutants.仅表达 Gli3 阻遏物的小鼠肢体类似于 Sonic hedgehog 突变体的肢体。
Dev Biol. 2013 Jul 15;379(2):221-8. doi: 10.1016/j.ydbio.2013.04.025. Epub 2013 May 2.

引用本文的文献

1
Proteomic profiling of primary cilia in the developing brain uncovers new regulators of cortical development.发育中大脑初级纤毛的蛋白质组分析揭示了皮质发育的新调节因子。
bioRxiv. 2025 May 4:2025.05.03.652041. doi: 10.1101/2025.05.03.652041.
2
Translation Fidelity and Respiration Deficits in CLPP-Deficient Tissues: Mechanistic Insights from Mitochondrial Complexome Profiling.CLPP 缺陷组织中的翻译保真度和呼吸缺陷:线粒体复合物组学分析的机制见解。
Int J Mol Sci. 2023 Dec 15;24(24):17503. doi: 10.3390/ijms242417503.
3
Controlling tissue patterning by translational regulation of signaling transcripts through the core translation factor eIF3c.通过核心翻译因子 eIF3c 对信号转录物的翻译调控控制组织模式形成。
Dev Cell. 2021 Nov 8;56(21):2928-2937.e9. doi: 10.1016/j.devcel.2021.10.009.
4
Giving translation a hand.为翻译助力。
Dev Cell. 2021 Nov 8;56(21):2921-2923. doi: 10.1016/j.devcel.2021.10.016.
5
Eukaryotic translation initiation factor 3 (eIF3) subunit e is essential for embryonic development and cell proliferation.真核生物翻译起始因子3(eIF3)的亚基e对胚胎发育和细胞增殖至关重要。
FEBS Open Bio. 2018 Jul 5;8(8):1188-1201. doi: 10.1002/2211-5463.12482. eCollection 2018 Aug.
6
Human eIF3b and eIF3a serve as the nucleation core for the assembly of eIF3 into two interconnected modules: the yeast-like core and the octamer.人类真核生物翻译起始因子3b(eIF3b)和真核生物翻译起始因子3a(eIF3a)作为真核生物翻译起始因子3(eIF3)组装成两个相互连接模块的成核核心:酵母样核心和八聚体。
Nucleic Acids Res. 2016 Dec 15;44(22):10772-10788. doi: 10.1093/nar/gkw972. Epub 2016 Oct 19.
7
Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model.用一个基础数学模型协调多种哺乳动物的色素沉着模式。
Nat Commun. 2016 Jan 6;7:10288. doi: 10.1038/ncomms10288.

本文引用的文献

1
The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival.p53肿瘤抑制因子在Rpl24基因缺陷型小鼠中会引发先天性畸形,并提高其存活率。
Mol Cell Biol. 2009 May;29(10):2489-504. doi: 10.1128/MCB.01588-08. Epub 2009 Mar 9.
2
Reconstitution reveals the functional core of mammalian eIF3.重组揭示了哺乳动物真核起始因子3(eIF3)的功能核心。
EMBO J. 2007 Jul 25;26(14):3373-83. doi: 10.1038/sj.emboj.7601765. Epub 2007 Jun 21.
3
eIF3: a versatile scaffold for translation initiation complexes.真核起始因子3:翻译起始复合物的多功能支架
Trends Biochem Sci. 2006 Oct;31(10):553-62. doi: 10.1016/j.tibs.2006.08.005. Epub 2006 Aug 22.
4
Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute.腹部斑点和尾巴(Bst)中的核糖体蛋白L24缺陷,一种小鼠微小体。
Development. 2004 Aug;131(16):3907-20. doi: 10.1242/dev.01268.
5
A dual role for Hox genes in limb anterior-posterior asymmetry.Hox基因在肢体前后不对称中的双重作用。
Science. 2004 Jun 11;304(5677):1669-72. doi: 10.1126/science.1096049.
6
Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh.与Hoxd蛋白的直接相互作用可逆转Gli3阻遏物的功能,从而在Shh下游促进指(趾)形成。
Development. 2004 May;131(10):2339-47. doi: 10.1242/dev.01115. Epub 2004 Apr 21.
7
Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning.Gremlin是肢体模式形成过程中维持Shh和Fgf信号所必需的骨形态发生蛋白拮抗剂。
Nat Genet. 2003 Jul;34(3):303-7. doi: 10.1038/ng1178.
8
The yeast eIF3 subunits TIF32/a, NIP1/c, and eIF5 make critical connections with the 40S ribosome in vivo.酵母真核生物翻译起始因子3(eIF3)的亚基TIF32/a、NIP1/c和eIF5在体内与40S核糖体形成关键连接。
Genes Dev. 2003 Mar 15;17(6):786-99. doi: 10.1101/gad.1065403.
9
Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud.小鼠GLI3调节发育中的神经管、面部和肢芽中的Fgf8表达及细胞凋亡。
Dev Biol. 2002 Nov 15;251(2):320-32. doi: 10.1006/dbio.2002.0811.
10
Direct eIF2-eIF3 contact in the multifactor complex is important for translation initiation in vivo.多因子复合物中eIF2与eIF3的直接接触对体内翻译起始很重要。
EMBO J. 2002 Nov 1;21(21):5886-98. doi: 10.1093/emboj/cdf563.

多效性小鼠表型多指斑点是由翻译起始因子 Eif3c 突变引起的,与 sonic hedgehog 信号通路的破坏有关。

The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.

机构信息

Institute for Biomedical Sciences, George Washington University, Washington, District of Columbia, USA.

出版信息

FASEB J. 2011 May;25(5):1596-605. doi: 10.1096/fj.10-169771. Epub 2011 Feb 3.

DOI:10.1096/fj.10-169771
PMID:21292980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3079303/
Abstract

Polydactyly is a common malformation and can be an isolated anomaly or part of a pleiotropic syndrome. The elucidation of the mutated genes that cause polydactyly provides insight into limb development pathways. The extra-toes spotting (Xs) mouse phenotype manifests anterior polydactyly, predominantly in the forelimbs, with ventral hypopigmenation. The mapping of Xs(J) to chromosome 7 was confirmed, and the interval was narrowed to 322 kb using intersubspecific crosses. Two mutations were identified in eukaryotic translation initiation factor 3 subunit C (Eif3c). An Eif3c c.907C>T mutation (p.Arg303X) was identified in Xs(J), and a c.1702_1758del mutation (p.Leu568_Leu586del) was identified in extra-toes spotting-like (Xsl), an allele of Xs(J). The effect of the Xs(J) mutation on the SHH/GLI3 pathway was analyzed by in situ hybridization analysis, and we show that Xs mouse embryos have ectopic Shh and Ptch1 expression in the anterior limb. In addition, anterior limb buds show aberrant Gli3 processing, consistent with perturbed SHH/GLI3 signaling. Based on the occurrence of Eif3c mutations in 2 Xs lines and haploinsufficiency of the Xs(J) allele, we conclude that the Xs phenotype is caused by a mutation in Eif3c, a component of the translation initiation complex, and that the phenotype is associated with aberrant SHH/GLI3 signaling.

摘要

多指畸形是一种常见的畸形,可作为孤立的异常,也可作为多效性综合征的一部分。阐明导致多指畸形的突变基因,为肢体发育途径提供了深入的了解。额外趾斑点(Xs)小鼠表型表现为前多指畸形,主要发生在前肢,并伴有腹侧色素减退。Xs(J)被映射到 7 号染色体,通过亚种间杂交将间隔缩小到 322 kb。在真核翻译起始因子 3 亚基 C(Eif3c)中鉴定出两个突变。Xs(J)中发现了 Eif3c c.907C>T 突变(p.Arg303X),Xs 样(Xsl)中发现了 c.1702_1758del 突变(p.Leu568_Leu586del),Xsl 是 Xs(J)的等位基因。通过原位杂交分析,分析了 Xs(J)突变对 SHH/GLI3 途径的影响,我们发现 Xs 小鼠胚胎在前肢中具有异位 Shh 和 Ptch1 表达。此外,前肢芽显示异常 Gli3 加工,与 SHH/GLI3 信号传导紊乱一致。基于 2 个 Xs 系中 Eif3c 突变的发生和 Xs(J)等位基因的单倍不足,我们得出结论,Xs 表型是由翻译起始复合物的组成部分 Eif3c 的突变引起的,并且表型与异常的 SHH/GLI3 信号传导有关。