• 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

基因捕获诱变:过去、现在及未来。

Gene-trap mutagenesis: past, present and beyond.

作者信息

Stanford W L, Cohn J B, Cordes S P

机构信息

Programme in Development and Fetal Health, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Room 983, Toronto, Ontario, Canada M5G 1X5.

出版信息

Nat Rev Genet. 2001 Oct;2(10):756-68. doi: 10.1038/35093548.

DOI:10.1038/35093548
PMID:11584292
Abstract

Although at least 35,000 human genes have been sequenced and mapped, adequate expression or functional information is available for only approximately 15% of them. Gene-trap mutagenesis is a technique that randomly generates loss-of-function mutations and reports the expression of many mouse genes. At present, several large-scale, gene-trap screens are being carried out with various new vectors, which aim to generate a public resource of mutagenized embryonic stem (ES) cells. This resource now includes more than 8,000 mutagenized ES-cell lines, which are freely available, making it an appropriate time to evaluate the recent advances in this area of genomic technology and the technical hurdles it has yet to overcome.

摘要

尽管至少35000个人类基因已被测序和定位,但只有约15%的基因有足够的表达或功能信息。基因捕获诱变是一种随机产生功能丧失突变并报告许多小鼠基因表达的技术。目前,正在使用各种新载体进行几项大规模的基因捕获筛选,目的是生成诱变胚胎干细胞(ES细胞)的公共资源。该资源现在包括8000多个诱变ES细胞系,这些细胞系可免费获取,这使得现在是评估这一基因组技术领域的最新进展及其尚未克服的技术障碍的适当时机。

相似文献

1
Gene-trap mutagenesis: past, present and beyond.基因捕获诱变:过去、现在及未来。
Nat Rev Genet. 2001 Oct;2(10):756-68. doi: 10.1038/35093548.
2
[Genetic screening for novel genes by insertional mutagenesis with gene trap method in ES cells].
Tanpakushitsu Kakusan Koso. 1995 Oct;40(14):2017-24.
3
Database for exchangeable gene trap clones: pathway and gene ontology analysis of exchangeable gene trap clone mouse lines.可交换基因打靶克隆数据库:可交换基因打靶克隆小鼠系的途径和基因本体分析。
Dev Growth Differ. 2014 Feb;56(2):161-74. doi: 10.1111/dgd.12116. Epub 2014 Jan 20.
4
Large-scale screening for developmental genes in embryonic stem cells and embryoid bodies using retroviral entrapment vectors.利用逆转录病毒捕获载体对胚胎干细胞和胚状体中的发育基因进行大规模筛选。
Dev Dyn. 1998 Jun;212(2):181-97. doi: 10.1002/(SICI)1097-0177(199806)212:2<181::AID-AJA4>3.0.CO;2-D.
5
Genomewide production of multipurpose alleles for the functional analysis of the mouse genome.用于小鼠基因组功能分析的多用途等位基因的全基因组产生。
Proc Natl Acad Sci U S A. 2005 May 17;102(20):7221-6. doi: 10.1073/pnas.0502273102. Epub 2005 May 3.
6
High-throughput trapping of secretory pathway genes in mouse embryonic stem cells.小鼠胚胎干细胞中分泌途径基因的高通量捕获
Nucleic Acids Res. 2006 Feb 13;34(3):e25. doi: 10.1093/nar/gnj026.
7
The gene trap resource: a treasure trove for hemopoiesis research.基因捕获资源:造血研究的宝库。
Exp Hematol. 2005 Aug;33(8):845-56. doi: 10.1016/j.exphem.2005.03.016.
8
[Discovery of genes active in embryogenesis by gene trapping].[通过基因捕获发现胚胎发育过程中活跃的基因]
Ontogenez. 2004 Jul-Aug;35(4):307-13.
9
Efficiency assessment of the gene trap approach.基因捕获方法的效率评估。
Dev Dyn. 1998 Jun;212(2):171-80. doi: 10.1002/(SICI)1097-0177(199806)212:2<171::AID-AJA3>3.0.CO;2-E.
10
Gene trap mutagenesis: a functional genomics approach towards reproductive research.基因捕获诱变:一种用于生殖研究的功能基因组学方法。
Mol Hum Reprod. 2007 Nov;13(11):771-9. doi: 10.1093/molehr/gam069. Epub 2007 Sep 23.

引用本文的文献

1
Non-viral intron knock-ins for targeted gene integration into human T cells and for T-cell selection.用于将目标基因整合到人类T细胞中以及用于T细胞选择的非病毒内含子敲入技术。
Nat Biomed Eng. 2025 Mar 7. doi: 10.1038/s41551-025-01372-1.
2
A versatile site-directed gene trap strategy to manipulate gene activity and control gene expression in Caenorhabditis elegans.一种通用的定点基因捕获策略,用于操纵秀丽隐杆线虫中的基因活性并控制基因表达。
PLoS Genet. 2025 Jan 22;21(1):e1011541. doi: 10.1371/journal.pgen.1011541. eCollection 2025 Jan.
3
Regional random mutagenesis driven by multiple sgRNAs and diverse on-target genome editing events to identify functionally important elements in non-coding regions.
利用多重 sgRNA 驱动的区域随机诱变和多种靶基因组编辑事件,鉴定非编码区中功能重要的元件。
Open Biol. 2024 Apr;14(4):240007. doi: 10.1098/rsob.240007. Epub 2024 Apr 3.
4
Integrating Omics and CRISPR Technology for Identification and Verification of Genomic Safe Harbor Loci in the Chicken Genome.整合组学与CRISPR技术用于鉴定和验证鸡基因组中的基因组安全港位点
Biol Proced Online. 2023 Jun 24;25(1):18. doi: 10.1186/s12575-023-00210-5.
5
Identification of genes contributing to cisplatin resistance in osteosarcoma cells.鉴定骨肉瘤细胞中顺铂耐药相关的基因。
FEBS Open Bio. 2023 Jan;13(1):164-173. doi: 10.1002/2211-5463.13524. Epub 2022 Nov 29.
6
Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish.神经肽相关组学和基因编辑的最新进展:聚焦 NPY 和生长抑素及其在鱼类生长和摄食中的作用。
Front Endocrinol (Lausanne). 2022 Oct 4;13:1023842. doi: 10.3389/fendo.2022.1023842. eCollection 2022.
7
Cathepsin B Gene Knockout Improves Behavioral Deficits and Reduces Pathology in Models of Neurologic Disorders.组织蛋白酶 B 基因敲除可改善神经疾病模型中的行为缺陷并减少病变。
Pharmacol Rev. 2022 Jul;74(3):600-629. doi: 10.1124/pharmrev.121.000527.
8
Complex response to physiological and drug-induced hepatic heme demand in monoallelic mice.单等位基因小鼠对生理和药物诱导的肝脏血红素需求的复杂反应。
Mol Genet Metab Rep. 2021 Nov 12;29:100818. doi: 10.1016/j.ymgmr.2021.100818. eCollection 2021 Dec.
9
A repackaged CRISPR platform increases homology-directed repair for yeast engineering.一种重新包装的 CRISPR 平台可提高酵母工程中的同源定向修复效率。
Nat Chem Biol. 2022 Jan;18(1):38-46. doi: 10.1038/s41589-021-00893-5. Epub 2021 Oct 28.
10
Applications of Transposons for Genome Manipulation in Stem Cells.转座子在干细胞基因组操作中的应用
Stem Cells Int. 2021 Sep 14;2021:3829286. doi: 10.1155/2021/3829286. eCollection 2021.