• 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

The evolution of WT1 sequence and expression pattern in the vertebrates.

作者信息

Kent J, Coriat A M, Sharpe P T, Hastie N D, van Heyningen V

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, Scotland, UK.

出版信息

Oncogene. 1995 Nov 2;11(9):1781-92.

PMID:7478606
Abstract

WT1 is a Wilms' tumour predisposition gene, encoding a protein with four C-terminal Kruppel-type zinc fingers, which is also a major regulator of kidney and gonadal development. To pinpoint key regulatory domains involved in development and evolution of the vertebrate genitourinary system, we have isolated WT1 orthologues from all gnathostome classes. Partial nucleotide sequence from chick, alligator, Xenopus laevis and zebrafish reveals extensive conservation. Both the zinc fingers and the transregulatory domain exhibit a high level of similarity in all the species examined. However, of the two alternatively spliced regions only one, the three amino acid KTS insertion between zinc fingers 3 and 4, is found in species other than mammals. The 17 amino acid insertion at the C-terminal end of the transregulatory domain is present only in mammals. Residues with reported human pathological mutations are also unaltered across species, underlining their structural significance. Studies in chick and alligator reveal that the mammalian intermediate mesoderm expression pattern is conserved in birds and reptiles. A wider role in mesodermal differentiation is suggested by expression in some paraxial and lateral mesoderm derivatives.

摘要

相似文献

1
The evolution of WT1 sequence and expression pattern in the vertebrates.
Oncogene. 1995 Nov 2;11(9):1781-92.
2
Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.迪尼-德拉斯综合征点突变对肾母细胞瘤抑制蛋白WT1的DNA结合活性的影响。
Biochemistry. 1996 Sep 17;35(37):12070-6. doi: 10.1021/bi960758o.
3
Expression in Xenopus oocytes shows that WT1 binds transcripts in vivo, with a central role for zinc finger one.非洲爪蟾卵母细胞中的表达表明,WT1在体内与转录本结合,锌指1起核心作用。
J Cell Sci. 2003 Apr 15;116(Pt 8):1539-49. doi: 10.1242/jcs.00324.
4
Did nucleotides or amino acids drive evolutionary conservation of the WT1 +/-KTS alternative splice?核苷酸还是氨基酸驱动了WT1+/-KTS可变剪接的进化保守性?
Hum Mol Genet. 2000 May 1;9(8):1177-83. doi: 10.1093/hmg/9.8.1177.
5
Eel WT1 sequence and expression in spontaneous nephroblastomas in Japanese eel.
Gene. 2000 Mar 21;245(2):245-51. doi: 10.1016/s0378-1119(00)00016-0.
6
Wilms' tumor 1 splice variants have opposite effects on the tumorigenicity of adenovirus-transformed baby-rat kidney cells.肾母细胞瘤1剪接变体对腺病毒转化的幼鼠肾细胞的致瘤性具有相反的作用。
Oncogene. 1996 Feb 1;12(3):537-46.
7
Wilms' tumour--a case of disrupted development.肾母细胞瘤——一例发育中断的病例。
J Cell Sci Suppl. 1994;18:1-5. doi: 10.1242/jcs.1994.supplement_18.1.
8
Wilms' tumor suppressor gene is involved in the development of disparate kidney forms: evidence from expression in the Xenopus pronephros.肾母细胞瘤抑癌基因参与不同肾脏形态的发育:来自非洲爪蟾前肾表达的证据。
Dev Dyn. 1996 Jun;206(2):131-8. doi: 10.1002/(SICI)1097-0177(199606)206:2<131::AID-AJA2>3.0.CO;2-J.
9
The Wilms tumour gene WT1 is expressed in murine mesoderm-derived tissues and mutated in a human mesothelioma.威尔姆斯瘤基因WT1在小鼠中胚层来源的组织中表达,并在一种人类间皮瘤中发生突变。
Nat Genet. 1993 Aug;4(4):415-20. doi: 10.1038/ng0893-415.
10
cDNA cloning and its pronephros-specific expression of the Wilms' tumor suppressor gene, WT1, from Xenopus laevis.
Gene. 1996 Oct 10;175(1-2):167-72. doi: 10.1016/0378-1119(96)00143-6.

引用本文的文献

1
RACK1 contributes to the upregulation of embryonic genes in a model of cardiac hypertrophy.RACK1 促进心肌肥厚模型中胚胎基因的上调。
Sci Rep. 2024 Oct 28;14(1):25698. doi: 10.1038/s41598-024-76138-x.
2
A Novel Mutation Identified in a 46,XX Testicular/Ovotesticular DSD Patient Results in the Retention of Intron 9.在一名46,XX性睾丸/卵睾型性发育障碍(DSD)患者中鉴定出的一种新型突变导致内含子9保留。
Biology (Basel). 2021 Nov 30;10(12):1248. doi: 10.3390/biology10121248.
3
Dose-response effects of light at night on the reproductive physiology of great tits (Parus major): Integrating morphological analyses with candidate gene expression.
夜间光照对大山雀(Parus major)生殖生理学的剂量反应效应:形态分析与候选基因表达的整合。
J Exp Zool A Ecol Integr Physiol. 2018 Oct;329(8-9):473-487. doi: 10.1002/jez.2214. Epub 2018 Jul 29.
4
Dysregulation of WTI (-KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation.WT1(-KTS)的失调与 LMX1B R246Q 突变的肾脏特异性效应有关。
Sci Rep. 2017 Jan 6;7:39933. doi: 10.1038/srep39933.
5
Identification of a Novel C-Terminal Truncated WT1 Isoform with Antagonistic Effects against Major WT1 Isoforms.一种对主要WT1亚型具有拮抗作用的新型C末端截短WT1亚型的鉴定。
PLoS One. 2015 Jun 19;10(6):e0130578. doi: 10.1371/journal.pone.0130578. eCollection 2015.
6
Oxygen-Dependent Gene Expression in Development and Cancer: Lessons Learned from the Wilms' Tumor Gene, WT1.发育和癌症中的氧依赖性基因表达:从 Wilms 瘤基因 WT1 中学到的教训。
Front Mol Neurosci. 2011 Feb 24;4:4. doi: 10.3389/fnmol.2011.00004. eCollection 2011.
7
Sex determination in the Squalius alburnoides complex: an initial characterization of sex cascade elements in the context of a hybrid polyploid genome.拟鲤复合种的性别决定:杂交多倍体基因组背景下性别级联元件的初步特征分析
PLoS One. 2009 Jul 28;4(7):e6401. doi: 10.1371/journal.pone.0006401.
8
Analyzing the coordinated gene network underlying temperature-dependent sex determination in reptiles.分析爬行动物温度依赖型性别决定背后的协同基因网络。
Semin Cell Dev Biol. 2009 May;20(3):293-303. doi: 10.1016/j.semcdb.2008.10.010. Epub 2008 Oct 30.
9
The Wilms tumor gene, Wt1, is required for Sox9 expression and maintenance of tubular architecture in the developing testis.威尔姆斯瘤基因Wt1是发育中的睾丸中Sox9表达和管状结构维持所必需的。
Proc Natl Acad Sci U S A. 2006 Aug 8;103(32):11987-92. doi: 10.1073/pnas.0600994103. Epub 2006 Jul 28.
10
The Wilms' tumor 1 (WT1) gene (+KTS isoform) functions with a CTE to enhance translation from an unspliced RNA with a retained intron.威尔姆斯瘤1(WT1)基因(+KTS异构体)与一个CTE共同作用,以增强从未剪接的带有保留内含子的RNA进行的翻译。
Genes Dev. 2006 Jun 15;20(12):1597-608. doi: 10.1101/gad.1402306. Epub 2006 May 31.