• 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

rVISTA 2.0:转录因子结合位点的进化分析

rVISTA 2.0: evolutionary analysis of transcription factor binding sites.

作者信息

Loots Gabriela G, Ovcharenko Ivan

机构信息

Genome Biology Division and EEBI Computing Division, Lawrence Livermore National Laboratory, 7000 East Avenue, L-441, Livermore, CA 94550, USA.

出版信息

Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W217-21. doi: 10.1093/nar/gkh383.

DOI:10.1093/nar/gkh383
PMID:15215384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC441521/
Abstract

Identifying and characterizing the transcription factor binding site (TFBS) patterns of cis-regulatory elements represents a challenge, but holds promise to reveal the regulatory language the genome uses to dictate transcriptional dynamics. Several studies have demonstrated that regulatory modules are under positive selection and, therefore, are often conserved between related species. Using this evolutionary principle, we have created a comparative tool, rVISTA, for analyzing the regulatory potential of noncoding sequences. Our ability to experimentally identify functional noncoding sequences is extremely limited, therefore, rVISTA attempts to fill this great gap in genomic analysis by offering a powerful approach for eliminating TFBSs least likely to be biologically relevant. The rVISTA tool combines TFBS predictions, sequence comparisons and cluster analysis to identify noncoding DNA regions that are evolutionarily conserved and present in a specific configuration within genomic sequences. Here, we present the newly developed version 2.0 of the rVISTA tool, which can process alignments generated by both the zPicture and blastz alignment programs or use pre-computed pairwise alignments of several vertebrate genomes available from the ECR Browser and GALA database. The rVISTA web server is closely interconnected with the TRANSFAC database, allowing users to either search for matrices present in the TRANSFAC library collection or search for user-defined consensus sequences. The rVISTA tool is publicly available at http://rvista.dcode.org/.

摘要

识别并表征顺式调控元件的转录因子结合位点(TFBS)模式是一项挑战,但有望揭示基因组用于支配转录动态的调控语言。多项研究表明,调控模块处于正选择之下,因此在相关物种之间通常是保守的。利用这一进化原理,我们创建了一种比较工具rVISTA,用于分析非编码序列的调控潜力。我们通过实验识别功能性非编码序列的能力极其有限,因此,rVISTA试图通过提供一种强大的方法来消除最不可能具有生物学相关性的TFBS,从而填补基因组分析中的这一巨大空白。rVISTA工具结合了TFBS预测、序列比较和聚类分析,以识别在基因组序列中进化保守且以特定构型存在的非编码DNA区域。在此,我们展示了新开发的rVISTA工具2.0版本,它可以处理由zPicture和blastz比对程序生成的比对结果,或者使用从ECR浏览器和GALA数据库获取的几个脊椎动物基因组的预先计算的成对比对结果。rVISTA网络服务器与TRANSFAC数据库紧密相连,允许用户搜索TRANSFAC文库集合中存在的矩阵,或搜索用户定义的共有序列。rVISTA工具可在http://rvista.dcode.org/上公开获取。

相似文献

1
rVISTA 2.0: evolutionary analysis of transcription factor binding sites.rVISTA 2.0:转录因子结合位点的进化分析
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W217-21. doi: 10.1093/nar/gkh383.
2
Dcode.org anthology of comparative genomic tools.Dcode.org比较基因组工具选集。
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W56-64. doi: 10.1093/nar/gki355.
3
ECR Browser: a tool for visualizing and accessing data from comparisons of multiple vertebrate genomes.ECR浏览器:一种用于可视化和访问来自多个脊椎动物基因组比较数据的工具。
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W280-6. doi: 10.1093/nar/gkh355.
4
MAPPER: a search engine for the computational identification of putative transcription factor binding sites in multiple genomes.MAPPER:一种用于在多个基因组中通过计算识别潜在转录因子结合位点的搜索引擎。
BMC Bioinformatics. 2005 Mar 30;6:79. doi: 10.1186/1471-2105-6-79.
5
Improvement of TRANSFAC matrices using multiple local alignment of transcription factor binding site sequences.利用转录因子结合位点序列的多重局部比对改进TRANSFAC矩阵。
Genome Inform. 2005;16(1):68-72.
6
CONREAL web server: identification and visualization of conserved transcription factor binding sites.CONREAL网络服务器:保守转录因子结合位点的识别与可视化
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W447-50. doi: 10.1093/nar/gki378.
7
ConSite: web-based prediction of regulatory elements using cross-species comparison.ConSite:利用跨物种比较对调控元件进行基于网络的预测。
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W249-52. doi: 10.1093/nar/gkh372.
8
SITECON: a tool for detecting conservative conformational and physicochemical properties in transcription factor binding site alignments and for site recognition.SITECON:一种用于检测转录因子结合位点比对中保守构象和物理化学性质以及用于位点识别的工具。
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W208-12. doi: 10.1093/nar/gkh474.
9
CREME: Cis-Regulatory Module Explorer for the human genome.CREME:人类基因组的顺式调控模块浏览器。
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W253-6. doi: 10.1093/nar/gkh385.
10
BLISS: binding site level identification of shared signal-modules in DNA regulatory sequences.BLISS:DNA调控序列中共享信号模块的结合位点水平鉴定
BMC Bioinformatics. 2006 Jun 7;7:287. doi: 10.1186/1471-2105-7-287.

引用本文的文献

1
Select early growth response (Egr) isoforms augment hypoxia inducible factor 2 (HIF-2) regulation of erythropoietin (Epo) gene expression in mammals.选择早期生长反应(Egr)亚型增强哺乳动物中缺氧诱导因子2(HIF-2)对促红细胞生成素(Epo)基因表达的调控。
J Biol Chem. 2025 Jun 10;301(7):110355. doi: 10.1016/j.jbc.2025.110355.
2
Complex Regulatory Interactions at GDF5 Shape Joint Morphology and Osteoarthritis Disease Risk.生长分化因子5处的复杂调控相互作用塑造关节形态和骨关节炎疾病风险。
Arthritis Rheumatol. 2025 May 12. doi: 10.1002/art.43231.
3
Mapping the transcriptional and epigenetic landscape of organotypic endothelial diversity in the developing and adult mouse.绘制发育中和成年小鼠器官型内皮多样性的转录和表观遗传图谱。
Nat Cardiovasc Res. 2025 Apr;4(4):473-495. doi: 10.1038/s44161-025-00618-0. Epub 2025 Mar 17.
4
The evaluation of transcription factor binding site prediction tools in human and Arabidopsis genomes.人类和拟南芥基因组中转录因子结合位点预测工具的评估
BMC Bioinformatics. 2024 Dec 2;25(1):371. doi: 10.1186/s12859-024-05995-0.
5
Complex regulatory interactions at shape joint morphology and osteoarthritis disease risk.复杂的调节相互作用塑造关节形态并影响骨关节炎疾病风险。
bioRxiv. 2024 Nov 1:2024.11.01.621374. doi: 10.1101/2024.11.01.621374.
6
Enrichment of -Acting Regulatory Elements in Differentially Methylated Regions Following Lipopolysaccharide Treatment of Bovine Endometrial Epithelial Cells.脂多糖处理牛子宫内膜上皮细胞后差异甲基化区域中 - 活性调控元件的富集。
Int J Mol Sci. 2024 Sep 11;25(18):9832. doi: 10.3390/ijms25189832.
7
The adhesion-GPCR ADGRF5 fuels breast cancer progression by suppressing the MMP8-mediated antitumorigenic effects.黏附 G 蛋白偶联受体 ADGRF5 通过抑制 MMP8 介导的抗肿瘤作用促进乳腺癌进展。
Cell Death Dis. 2024 Jun 27;15(6):455. doi: 10.1038/s41419-024-06855-8.
8
HOXC6 drives a therapeutically targetable pancreatic cancer growth and metastasis pathway by regulating MSK1 and PPP2R2B.HOXC6 通过调控 MSK1 和 PPP2R2B 驱动可治疗的胰腺癌生长和转移途径。
Cell Rep Med. 2023 Nov 21;4(11):101285. doi: 10.1016/j.xcrm.2023.101285. Epub 2023 Nov 10.
9
Comparative analysis of the myoglobin gene in whales and humans reveals evolutionary changes in regulatory elements and expression levels.比较鲸鱼和人类的肌红蛋白基因,揭示了调控元件和表达水平的进化变化。
PLoS One. 2023 Aug 29;18(8):e0284834. doi: 10.1371/journal.pone.0284834. eCollection 2023.
10
IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma.相邻NHEJ1内含子内的IHH增强子变异导致小眼症、无眼症和脉络膜缺损。
NPJ Genom Med. 2023 Aug 14;8(1):22. doi: 10.1038/s41525-023-00364-x.

本文引用的文献

1
zPicture: dynamic alignment and visualization tool for analyzing conservation profiles.zPicture:用于分析保守概况的动态比对和可视化工具。
Genome Res. 2004 Mar;14(3):472-7. doi: 10.1101/gr.2129504.
2
MATCH: A tool for searching transcription factor binding sites in DNA sequences.MATCH:一种用于在DNA序列中搜索转录因子结合位点的工具。
Nucleic Acids Res. 2003 Jul 1;31(13):3576-9. doi: 10.1093/nar/gkg585.
3
Human-mouse alignments with BLASTZ.使用BLASTZ进行人-小鼠序列比对。
Genome Res. 2003 Jan;13(1):103-7. doi: 10.1101/gr.809403.
4
TRANSFAC: transcriptional regulation, from patterns to profiles.TRANSFAC:转录调控,从模式到图谱。
Nucleic Acids Res. 2003 Jan 1;31(1):374-8. doi: 10.1093/nar/gkg108.
5
Initial sequencing and comparative analysis of the mouse genome.小鼠基因组的初步测序与比较分析。
Nature. 2002 Dec 5;420(6915):520-62. doi: 10.1038/nature01262.
6
Fast algorithms for large-scale genome alignment and comparison.用于大规模基因组比对和比较的快速算法。
Nucleic Acids Res. 2002 Jun 1;30(11):2478-83. doi: 10.1093/nar/30.11.2478.
7
rVista for comparative sequence-based discovery of functional transcription factor binding sites.rVista用于基于序列比较发现功能性转录因子结合位点。
Genome Res. 2002 May;12(5):832-9. doi: 10.1101/gr.225502.
8
Cardiac-specific activity of an Nkx2-5 enhancer requires an evolutionarily conserved Smad binding site.Nkx2-5增强子的心脏特异性活性需要一个进化上保守的Smad结合位点。
Dev Biol. 2002 Apr 15;244(2):257-66. doi: 10.1006/dbio.2002.0603.
9
Nkx-2.5 gene induction in mice is mediated by a Smad consensus regulatory region.小鼠中Nkx-2.5基因的诱导由Smad共有调控区域介导。
Dev Biol. 2002 Apr 15;244(2):243-56. doi: 10.1006/dbio.2002.0604.
10
The sequence of the human genome.人类基因组序列。
Science. 2001 Feb 16;291(5507):1304-51. doi: 10.1126/science.1058040.