• 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

CEAS:顺式调控元件注释系统。

CEAS: cis-regulatory element annotation system.

作者信息

Ji Xuwo, Li Wei, Song Jun, Wei Liping, Liu X Shirley

机构信息

Center for Bioinformatics, National Laboratory of Protein Engineering and Plant Genetic Engineering, College of Life Sciences, Peking University Beijing, People's Republic China 100871.

出版信息

Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W551-4. doi: 10.1093/nar/gkl322.

DOI:10.1093/nar/gkl322
PMID:16845068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1538818/
Abstract

The recent availability of high-density human genome tiling arrays enables biologists to conduct ChIP-chip experiments to locate the in vivo-binding sites of transcription factors in the human genome and explore the regulatory mechanisms. Once genomic regions enriched by transcription factor ChIP-chip are located, genome-scale downstream analyses are crucial but difficult for biologists without strong bioinformatics support. We designed and implemented the first web server to streamline the ChIP-chip downstream analyses. Given genome-scale ChIP regions, the cis-regulatory element annotation system (CEAS) retrieves repeat-masked genomic sequences, calculates GC content, plots evolutionary conservation, maps nearby genes and identifies enriched transcription factor-binding motifs. Biologists can utilize CEAS to retrieve useful information for ChIP-chip validation, assemble important knowledge to include in their publication and generate novel hypotheses (e.g. transcription factor cooperative partner) for further study. CEAS helps the adoption of ChIP-chip in mammalian systems and provides insights towards a more comprehensive understanding of transcriptional regulatory mechanisms. The URL of the server is http://ceas.cbi.pku.edu.cn.

摘要

近期高密度人类基因组平铺阵列的出现,使生物学家能够开展染色质免疫沉淀芯片(ChIP-chip)实验,以定位人类基因组中转录因子的体内结合位点,并探索调控机制。一旦通过ChIP-chip确定了富含转录因子的基因组区域,对于没有强大生物信息学支持的生物学家来说,全基因组规模的下游分析至关重要但却困难重重。我们设计并实现了首个用于简化ChIP-chip下游分析的网络服务器。给定全基因组规模的ChIP区域,顺式调控元件注释系统(CEAS)可检索重复序列屏蔽的基因组序列、计算GC含量、绘制进化保守性图谱、定位附近基因并识别富集的转录因子结合基序。生物学家可利用CEAS检索用于ChIP-chip验证的有用信息,整合重要知识以便在其发表成果中纳入,并生成新的假设(如转录因子合作伙伴)以供进一步研究。CEAS有助于在哺乳动物系统中采用ChIP-chip,并为更全面地理解转录调控机制提供见解。该服务器的网址为http://ceas.cbi.pku.edu.cn。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/1538818/f6e782708c0d/gkl322f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/1538818/f6e782708c0d/gkl322f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/1538818/f6e782708c0d/gkl322f1.jpg

相似文献

1
CEAS: cis-regulatory element annotation system.CEAS:顺式调控元件注释系统。
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W551-4. doi: 10.1093/nar/gkl322.
2
CEAS: cis-regulatory element annotation system.CEAS:顺式调控元件注释系统。
Bioinformatics. 2009 Oct 1;25(19):2605-6. doi: 10.1093/bioinformatics/btp479. Epub 2009 Aug 18.
3
MPromDb: an integrated resource for annotation and visualization of mammalian gene promoters and ChIP-chip experimental data.MPromDb:用于哺乳动物基因启动子注释和可视化以及芯片实验数据的综合资源。
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D98-103. doi: 10.1093/nar/gkj096.
4
A comparative analysis of genome-wide chromatin immunoprecipitation data for mammalian transcription factors.哺乳动物转录因子全基因组染色质免疫沉淀数据的比较分析。
Nucleic Acids Res. 2006;34(21):e146. doi: 10.1093/nar/gkl803. Epub 2006 Nov 7.
5
Stubb: a program for discovery and analysis of cis-regulatory modules.Stubb:一个用于发现和分析顺式调控模块的程序。
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W555-9. doi: 10.1093/nar/gkl224.
6
Using CisGenome to analyze ChIP-chip and ChIP-seq data.使用CisGenome分析染色质免疫沉淀芯片(ChIP-chip)和染色质免疫沉淀测序(ChIP-seq)数据。
Curr Protoc Bioinformatics. 2011 Mar;Chapter 2:Unit2.13. doi: 10.1002/0471250953.bi0213s33.
7
PeakAnalyzer: genome-wide annotation of chromatin binding and modification loci.PeakAnalyzer:全基因组注释染色质结合和修饰基因座。
BMC Bioinformatics. 2010 Aug 6;11:415. doi: 10.1186/1471-2105-11-415.
8
A hidden Markov model for analyzing ChIP-chip experiments on genome tiling arrays and its application to p53 binding sequences.一种用于分析基因组平铺阵列上的染色质免疫沉淀芯片实验的隐马尔可夫模型及其在p53结合序列中的应用。
Bioinformatics. 2005 Jun;21 Suppl 1:i274-82. doi: 10.1093/bioinformatics/bti1046.
9
TFBScluster web server for the identification of mammalian composite regulatory elements.用于识别哺乳动物复合调控元件的TFBScluster网络服务器。
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W524-8. doi: 10.1093/nar/gkl041.
10
GSDS 2.0: an upgraded gene feature visualization server.基因结构显示服务器2.0:一个升级的基因特征可视化服务器。
Bioinformatics. 2015 Apr 15;31(8):1296-7. doi: 10.1093/bioinformatics/btu817. Epub 2014 Dec 10.

引用本文的文献

1
Protocol for transcriptomic and epigenomic analyses of tip-like endothelial cells using scRNA-seq and ChIP-seq.使用单细胞RNA测序(scRNA-seq)和染色质免疫沉淀测序(ChIP-seq)对类顶端内皮细胞进行转录组和表观基因组分析的方案。
STAR Protoc. 2025 Mar 21;6(1):103326. doi: 10.1016/j.xpro.2024.103326. Epub 2025 Jan 10.
2
Nuclear microRNA 9 mediates G-quadruplex formation and 3D genome organization during TGF-β-induced transcription.核微小RNA 9在转化生长因子-β诱导的转录过程中介导G-四链体的形成和三维基因组组织。
Nat Commun. 2024 Dec 20;15(1):10711. doi: 10.1038/s41467-024-54740-x.
3
The CoREST repressor complex mediates phenotype switching and therapy resistance in melanoma.

本文引用的文献

1
Core transcriptional regulatory circuitry in human embryonic stem cells.人类胚胎干细胞中的核心转录调控回路。
Cell. 2005 Sep 23;122(6):947-56. doi: 10.1016/j.cell.2005.08.020.
2
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.脊椎动物、昆虫、蠕虫和酵母基因组中的进化保守元件。
Genome Res. 2005 Aug;15(8):1034-50. doi: 10.1101/gr.3715005. Epub 2005 Jul 15.
3
Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the forkhead protein FoxA1.雌激素受体结合的全染色体图谱揭示了需要叉头蛋白FoxA1的长程调控。
CoREST 抑制复合物介导黑色素瘤的表型转换和治疗抵抗。
J Clin Invest. 2024 Feb 1;134(6):e171063. doi: 10.1172/JCI171063.
4
Luminal breast cancer identity is determined by loss of glucocorticoid receptor activity.腔面型乳腺癌的特征是糖皮质激素受体活性丧失。
EMBO Mol Med. 2023 Dec 7;15(12):e17737. doi: 10.15252/emmm.202317737. Epub 2023 Oct 30.
5
Integrating genetics with single-cell multiomic measurements across disease states identifies mechanisms of beta cell dysfunction in type 2 diabetes.将遗传学与疾病状态下的单细胞多组学测量相结合,确定了 2 型糖尿病中β细胞功能障碍的机制。
Nat Genet. 2023 Jun;55(6):984-994. doi: 10.1038/s41588-023-01397-9. Epub 2023 May 25.
6
Integration of single-cell multiomic measurements across disease states with genetics identifies mechanisms of beta cell dysfunction in type 2 diabetes.整合跨疾病状态的单细胞多组学测量与遗传学,可确定2型糖尿病中β细胞功能障碍的机制。
bioRxiv. 2023 Jan 2:2022.12.31.522386. doi: 10.1101/2022.12.31.522386.
7
TERRA regulates DNA G-quadruplex formation and ATRX recruitment to chromatin.TERRA 调节 DNA G-四链体的形成和 ATRX 向染色质的募集。
Nucleic Acids Res. 2022 Nov 28;50(21):12217-12234. doi: 10.1093/nar/gkac1114.
8
2cChIP-seq and 2cMeDIP-seq: The Carrier-Assisted Methods for Epigenomic Profiling of Small Cell Numbers or Single Cells.2cChIP-seq 和 2cMeDIP-seq:用于小细胞数量或单细胞的表观基因组分析的载体辅助方法。
Int J Mol Sci. 2022 Nov 12;23(22):13984. doi: 10.3390/ijms232213984.
9
Characterization of HCI-EC-23 a novel estrogen- and progesterone-responsive endometrial cancer cell line.HCI-EC-23 细胞系的特征:一种新型的雌激素和孕激素反应性子宫内膜癌细胞系。
Sci Rep. 2022 Nov 17;12(1):19731. doi: 10.1038/s41598-022-24211-8.
10
Subtype heterogeneity and epigenetic convergence in neuroendocrine prostate cancer.神经内分泌前列腺癌的亚型异质性和表观遗传趋同。
Nat Commun. 2021 Oct 1;12(1):5775. doi: 10.1038/s41467-021-26042-z.
Cell. 2005 Jul 15;122(1):33-43. doi: 10.1016/j.cell.2005.05.008.
4
A high-resolution map of active promoters in the human genome.人类基因组中活跃启动子的高分辨率图谱。
Nature. 2005 Aug 11;436(7052):876-80. doi: 10.1038/nature03877. Epub 2005 Jun 29.
5
Genomic maps and comparative analysis of histone modifications in human and mouse.人类和小鼠的基因组图谱及组蛋白修饰的比较分析
Cell. 2005 Jan 28;120(2):169-81. doi: 10.1016/j.cell.2005.01.001.
6
Transcriptional regulatory code of a eukaryotic genome.真核生物基因组的转录调控密码
Nature. 2004 Sep 2;431(7004):99-104. doi: 10.1038/nature02800.
7
A suite of web-based programs to search for transcriptional regulatory motifs.一套用于搜索转录调控基序的基于网络的程序。
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W204-7. doi: 10.1093/nar/gkh461.
8
WebLogo: a sequence logo generator.WebLogo:一个序列图生成器。
Genome Res. 2004 Jun;14(6):1188-90. doi: 10.1101/gr.849004.
9
CREB binds to multiple loci on human chromosome 22.CREB与人类22号染色体上的多个基因座结合。
Mol Cell Biol. 2004 May;24(9):3804-14. doi: 10.1128/MCB.24.9.3804-3814.2004.
10
Unbiased mapping of transcription factor binding sites along human chromosomes 21 and 22 points to widespread regulation of noncoding RNAs.沿着人类21号和22号染色体对转录因子结合位点进行的无偏差定位表明非编码RNA受到广泛调控。
Cell. 2004 Feb 20;116(4):499-509. doi: 10.1016/s0092-8674(04)00127-8.