• 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

秀丽隐杆线虫FoxA蛋白PHA-4对器官发生的调控

Regulation of organogenesis by the Caenorhabditis elegans FoxA protein PHA-4.

作者信息

Gaudet J, Mango S E

机构信息

Huntsman Cancer Institute, University of Utah, 2000 Circle of Hope, Salt Lake City, UT 84112, USA.

出版信息

Science. 2002 Feb 1;295(5556):821-5. doi: 10.1126/science.1065175.

DOI:10.1126/science.1065175
PMID:11823633
Abstract

The pha-4 locus encodes a forkhead box A (FoxA/HNF3) transcription factor homolog that specifies organ identity for Caenorhabditis elegans pharyngeal cells. We used microarrays to identify pharyngeal genes and analyzed those genes to determine which were direct PHA-4 targets. Our data suggest that PHA-4 directly activates most or all pharyngeal genes. Furthermore, the relative affinity of PHA-4 for different TRTTKRY (R = A/G, K = T/G, Y = T/C) elements modulates the onset of gene expression, providing a mechanism to activate pharyngeal genes at different developmental stages. We suggest that direct transcriptional regulation of entire gene networks may be a common feature of organ identity genes.

摘要

pha-4基因座编码一种叉头框A(FoxA/HNF3)转录因子同源物,它决定了秀丽隐杆线虫咽部细胞的器官特性。我们使用微阵列来鉴定咽部基因,并分析这些基因以确定哪些是PHA-4的直接靶标。我们的数据表明,PHA-4直接激活了大多数或所有咽部基因。此外,PHA-4对不同TRTTKRY(R = A/G,K = T/G,Y = T/C)元件的相对亲和力调节了基因表达的起始,为在不同发育阶段激活咽部基因提供了一种机制。我们认为,对整个基因网络的直接转录调控可能是器官特性基因的一个共同特征。

相似文献

1
Regulation of organogenesis by the Caenorhabditis elegans FoxA protein PHA-4.秀丽隐杆线虫FoxA蛋白PHA-4对器官发生的调控
Science. 2002 Feb 1;295(5556):821-5. doi: 10.1126/science.1065175.
2
Transcription factors GATA/ELT-2 and forkhead/HNF-3/PHA-4 regulate the tropomyosin gene expression in the pharynx and intestine of Caenorhabditis elegans.转录因子GATA/ELT-2和叉头框/HNF-3/PHA-4调控秀丽隐杆线虫咽部和肠道中原肌球蛋白基因的表达。
J Mol Biol. 2008 May 30;379(2):201-11. doi: 10.1016/j.jmb.2007.11.103. Epub 2007 Dec 7.
3
pha-2 encodes the C. elegans ortholog of the homeodomain protein HEX and is required for the formation of the pharyngeal isthmus.pha-2编码同源结构域蛋白HEX的秀丽隐杆线虫直系同源物,是咽峡形成所必需的。
Dev Biol. 2004 Aug 15;272(2):403-18. doi: 10.1016/j.ydbio.2004.05.011.
4
In vitro and in vivo characterization of Caenorhabditis elegans PHA-4/FoxA response elements.秀丽隐杆线虫 PHA-4/FoxA 反应元件的体外和体内特性分析。
Dev Dyn. 2010 Aug;239(8):2219-32. doi: 10.1002/dvdy.22359.
5
Development of Caenorhabditis elegans pharynx, with emphasis on its nervous system.秀丽隐杆线虫咽的发育,重点关注其神经系统。
Acta Pharmacol Sin. 2005 Apr;26(4):396-404. doi: 10.1111/j.1745-7254.2005.00070.x.
6
Coordination of ges-1 expression between the Caenorhabditis pharynx and intestine.秀丽隐杆线虫咽和肠中ges-1表达的协调。
Dev Biol. 2001 Nov 15;239(2):350-63. doi: 10.1006/dbio.2001.0442.
7
The third and fourth tropomyosin isoforms of Caenorhabditis elegans are expressed in the pharynx and intestines and are essential for development and morphology.秀丽隐杆线虫的第三种和第四种原肌球蛋白亚型在咽部和肠道中表达,对发育和形态至关重要。
J Mol Biol. 2001 Oct 26;313(3):525-37. doi: 10.1006/jmbi.2001.5052.
8
pha-4 is Ce-fkh-1, a fork head/HNF-3alpha,beta,gamma homolog that functions in organogenesis of the C. elegans pharynx.pha-4即Ce-fkh-1,是一种叉头框/HNF-3α、β、γ同源物,在秀丽隐杆线虫咽的器官发生中发挥作用。
Development. 1998 Jun;125(12):2171-80. doi: 10.1242/dev.125.12.2171.
9
Gland-specific expression of C. elegans hlh-6 requires the combinatorial action of three distinct promoter elements.秀丽隐杆线虫hlh-6的腺体特异性表达需要三种不同启动子元件的组合作用。
Dev Biol. 2007 Feb 1;302(1):295-308. doi: 10.1016/j.ydbio.2006.09.036. Epub 2006 Sep 26.
10
PHA-4/FoxA cooperates with TAM-1/TRIM to regulate cell fate restriction in the C. elegans foregut.PHA-4/FoxA与TAM-1/TRIM协同作用,调控秀丽隐杆线虫前肠中的细胞命运限制。
Dev Biol. 2007 Mar 15;303(2):611-24. doi: 10.1016/j.ydbio.2006.11.042. Epub 2006 Dec 2.

引用本文的文献

1
Multiple overlapping binding sites determine transcription factor occupancy.多个重叠结合位点决定转录因子占据情况。
Nature. 2025 Sep 3. doi: 10.1038/s41586-025-09472-3.
2
The combinatorial binding syntax of transcription factors in forebrain-specific enhancers.前脑特异性增强子中转录因子的组合结合语法。
Biol Open. 2025 Feb 15;14(2). doi: 10.1242/bio.061751. Epub 2025 Feb 19.
3
Optimization of the Irf8 +32-kb enhancer disrupts dendritic cell lineage segregation.优化 Irf8 +32-kb 增强子会破坏树突状细胞谱系分离。
Nat Immunol. 2024 Nov;25(11):2043-2056. doi: 10.1038/s41590-024-01976-w. Epub 2024 Oct 7.
4
A suboptimal OCT4-SOX2 binding site facilitates the naïve-state specific function of a Klf4 enhancer.一个不理想的 OCT4-SOX2 结合位点促进了 Klf4 增强子的原始态特异性功能。
PLoS One. 2024 Sep 30;19(9):e0311120. doi: 10.1371/journal.pone.0311120. eCollection 2024.
5
Single-tissue proteomics in reveals proteins resident in intestinal lysosome-related organelles.揭示肠道溶酶体相关细胞器中驻留蛋白的单细胞蛋白质组学。
Proc Natl Acad Sci U S A. 2024 Jun 18;121(25):e2322588121. doi: 10.1073/pnas.2322588121. Epub 2024 Jun 11.
6
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues.在家蝶结构域中稀有变异的 DNA 结合分析揭示了决定同源结构域特异性的残基。
Nat Commun. 2024 Apr 10;15(1):3110. doi: 10.1038/s41467-024-47396-0.
7
A lineage-resolved cartography of microRNA promoter activity in C. elegans empowers multidimensional developmental analysis.线虫中 miRNA 启动子活性的谱系解析图谱为多维发育分析提供了支持。
Nat Commun. 2024 Mar 30;15(1):2783. doi: 10.1038/s41467-024-47055-4.
8
Mechanisms of lineage specification in Caenorhabditis elegans.线虫中谱系特化的机制。
Genetics. 2023 Dec 6;225(4). doi: 10.1093/genetics/iyad174.
9
Whole-body gene expression atlas of an adult metazoan.成年后生体的全基因组表达图谱。
Sci Adv. 2023 Jun 23;9(25):eadg0506. doi: 10.1126/sciadv.adg0506.
10
Systematic analysis of low-affinity transcription factor binding site clusters in vitro and in vivo establishes their functional relevance.系统分析体外和体内低亲和力转录因子结合位点簇,确定其功能相关性。
Nat Commun. 2022 Sep 7;13(1):5273. doi: 10.1038/s41467-022-32971-0.