• 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

相似文献

1
Cautionary insights on knockout mouse studies: the gene or not the gene?对基因敲除小鼠研究的警示性见解:是基因还是非基因?
Brain Behav Immun. 2009 Mar;23(3):318-24. doi: 10.1016/j.bbi.2008.09.001. Epub 2008 Sep 12.
2
Unexpected embryonic stem (ES) cell mutations represent a concern in gene targeting: lessons from "fierce" mice.意外的胚胎干细胞(ES细胞)突变是基因靶向中的一个问题:来自“凶猛”小鼠的教训。
Genesis. 2004 Feb;38(2):51-7. doi: 10.1002/gene.20001.
3
[Genetic modification of the mouse].[小鼠的基因改造]
Tidsskr Nor Laegeforen. 1998 Oct 20;118(25):3952-7.
4
Conditional knockout mice.条件性基因敲除小鼠
Methods Mol Biol. 2003;209:159-85. doi: 10.1385/1-59259-340-2:159.
5
Knockout mice: simple solutions to the problems of genetic background and flanking genes.基因敲除小鼠:解决遗传背景和侧翼基因问题的简单方法。
Trends Neurosci. 2002 Jul;25(7):336-40. doi: 10.1016/s0166-2236(02)02192-6.
6
Gene trap and gene inversion methods for conditional gene inactivation in the mouse.用于小鼠条件性基因失活的基因捕获和基因倒置方法。
Nucleic Acids Res. 2005 Jan 19;33(2):e14. doi: 10.1093/nar/gni016.
7
Mouse genome modification.小鼠基因组改造
Methods Mol Med. 2003;89:529-44. doi: 10.1385/1-59259-419-0:529.
8
Gene targeting in the mouse.小鼠中的基因靶向
Methods Mol Biol. 2011;770:293-312. doi: 10.1007/978-1-61779-210-6_11.
9
Optimized vector for conditional gene targeting in mouse embryonic stem cells.用于小鼠胚胎干细胞中条件性基因靶向的优化载体。
Biotechniques. 2003 Jun;34(6):1136-8, 1140. doi: 10.2144/03346bm03.
10
"Gene-swap knock-in" cassette in mice to study allelic differences in human genes.用于研究人类基因等位基因差异的小鼠“基因交换敲入”盒。
Ann N Y Acad Sci. 2000;919:148-70. doi: 10.1111/j.1749-6632.2000.tb06876.x.

引用本文的文献

1
Suppression of Skp2 contributes to sepsis-induced acute lung injury by enhancing ferroptosis through the ubiquitination of SLC3A2.抑制 Skp2 通过泛素化 SLC3A2 促进铁死亡来加重脓毒症诱导的急性肺损伤。
Cell Mol Life Sci. 2024 Jul 30;81(1):325. doi: 10.1007/s00018-024-05348-3.
2
txci-ATAC-seq: a massive-scale single-cell technique to profile chromatin accessibility.txci-ATAC-seq:一种大规模的单细胞技术,用于描绘染色质可及性。
Genome Biol. 2024 Mar 22;25(1):78. doi: 10.1186/s13059-023-03150-1.
3
Three Main SCFAs Mitigate Lung Inflammation and Tissue Remodeling Nlrp3-Dependent in Murine HDM-Induced Neutrophilic Asthma.三种主要的短链脂肪酸通过 Nlrp3 依赖途径减轻小鼠变应原诱导的中性粒细胞性哮喘的肺部炎症和组织重塑。
Inflammation. 2024 Aug;47(4):1386-1402. doi: 10.1007/s10753-024-01983-x. Epub 2024 Feb 8.
4
Stereotactic Delivery of Helper-dependent Adenoviral Viral Vectors at Distinct Developmental Time Points to Perform Age-dependent Molecular Manipulations of the Mouse Calyx of Held.在不同发育时间点立体定向递送辅助依赖型腺病毒载体,以对小鼠Held壶腹进行年龄依赖性分子操作。
Bio Protoc. 2023 Aug 20;13(16):e4793. doi: 10.21769/BioProtoc.4793.
5
The Impact of CC16 on Pulmonary Epithelial-Driven Host Responses during Infection in Mouse Tracheal Epithelial Cells.CC16 对小鼠气管上皮细胞感染期间肺上皮细胞驱动的宿主反应的影响。
Cells. 2023 Aug 1;12(15):1984. doi: 10.3390/cells12151984.
6
A Rat Model of the Brain-Derived Neurotrophic Factor Val66Met Polymorphism Shows Attenuated Motivation for Alcohol Self-Administration and Diminished Propensity for Cue-Induced Relapse in Females.脑源性神经营养因子Val66Met多态性的大鼠模型显示,雌性大鼠对酒精自我给药的动机减弱,线索诱导复吸的倾向降低。
Biology (Basel). 2023 May 31;12(6):799. doi: 10.3390/biology12060799.
7
Hardwiring tissue-specific AAV transduction in mice through engineered receptor expression.通过工程化受体表达,在小鼠中实现组织特异性 AAV 转导的固定化。
Nat Methods. 2023 Jul;20(7):1070-1081. doi: 10.1038/s41592-023-01896-x. Epub 2023 Jun 8.
8
Activating Transcription Factor 3 Diminishes Ischemic Cerebral Infarct and Behavioral Deficit by Downregulating Carboxyl-Terminal Modulator Protein.激活转录因子 3 通过下调羧基末端调制蛋白减少缺血性脑梗死和行为缺陷。
Int J Mol Sci. 2023 Jan 24;24(3):2306. doi: 10.3390/ijms24032306.
9
Investigating the Influence of Anaesthesiology for Cancer Resection Surgery on Oncologic Outcomes: The Role of Experimental In Vivo Models.探讨麻醉学对癌症切除术的肿瘤学结果的影响:实验体内模型的作用。
Medicina (Kaunas). 2022 Oct 1;58(10):1380. doi: 10.3390/medicina58101380.
10
The Angiotensin AT Receptor: From a Binding Site to a Novel Therapeutic Target.血管紧张素 AT 受体:从结合位点到新的治疗靶点。
Pharmacol Rev. 2022 Oct;74(4):1051-1135. doi: 10.1124/pharmrev.120.000281.

本文引用的文献

1
Mitigation of experimental allergic encephalomyelitis by TGF-beta induced Foxp3+ regulatory T lymphocytes through the induction of anergy and infectious tolerance.转化生长因子-β通过诱导无反应性和感染耐受来诱导Foxp3+调节性T淋巴细胞,从而减轻实验性变应性脑脊髓炎。
J Immunol. 2008 Mar 1;180(5):2830-8. doi: 10.4049/jimmunol.180.5.2830.
2
Molecular mechanism of lipopolysaccharide-induced SOCS-3 gene expression in macrophages and microglia.脂多糖诱导巨噬细胞和小胶质细胞中SOCS-3基因表达的分子机制
J Immunol. 2007 Nov 1;179(9):5966-76. doi: 10.4049/jimmunol.179.9.5966.
3
Relevance of BAC transgene copy number in mice: transgene copy number variation across multiple transgenic lines and correlations with transgene integrity and expression.BAC转基因拷贝数在小鼠中的相关性:多个转基因品系间的转基因拷贝数变异及其与转基因完整性和表达的相关性
Mamm Genome. 2007 Oct;18(10):693-708. doi: 10.1007/s00335-007-9056-y. Epub 2007 Sep 20.
4
New tools for defining the 'genetic background' of inbred mouse strains.用于定义近交系小鼠品系“遗传背景”的新工具。
Nat Immunol. 2007 Jul;8(7):669-73. doi: 10.1038/ni0707-669.
5
A mouse for all reasons.适用于各种情况的小鼠。
Cell. 2007 Jan 12;128(1):9-13. doi: 10.1016/j.cell.2006.12.018.
6
Mouse strain differences in autonomic responses to stress.小鼠品系对应激自主反应的差异。
Genes Brain Behav. 2006 Mar;5(2):139-49. doi: 10.1111/j.1601-183X.2005.00143.x.
7
Two new behavioral QTLs, Emo4 and Reb1, map to mouse Chromosome 1: Congenic strains and candidate gene identification studies.两个新的行为学数量性状基因座Emo4和Reb1定位于小鼠1号染色体:同源近交系和候选基因鉴定研究。
Mamm Genome. 2006 Feb;17(2):111-8. doi: 10.1007/s00335-005-0107-y. Epub 2006 Feb 7.
8
Contrasting grooming phenotypes in C57Bl/6 and 129S1/SvImJ mice.C57Bl/6和129S1/SvImJ小鼠不同的修饰表型
Brain Res. 2004 Nov 26;1028(1):75-82. doi: 10.1016/j.brainres.2004.09.001.
9
Induction of low dose oral tolerance in IL-10 deficient mice with experimental autoimmune encephalomyelitis.在患有实验性自身免疫性脑脊髓炎的白细胞介素-10缺陷小鼠中诱导低剂量口服耐受。
J Autoimmun. 2004 Nov;23(3):193-200. doi: 10.1016/j.jaut.2004.08.001.
10
Correlations between behaviours in the elevated plus-maze and sensitivity to unpredictable subchronic mild stress: evidence from inbred strains of mice.高架十字迷宫中的行为与对不可预测的亚慢性轻度应激的敏感性之间的相关性:来自近交系小鼠的证据。
Behav Brain Res. 2005 Jan 6;156(1):153-62. doi: 10.1016/j.bbr.2004.05.018.

对基因敲除小鼠研究的警示性见解:是基因还是非基因?

Cautionary insights on knockout mouse studies: the gene or not the gene?

作者信息

Eisener-Dorman Amy F, Lawrence David A, Bolivar Valerie J

机构信息

Wadsworth Center, 120 New Scotland Avenue, David Axelrod Institute, Albany, NY 12208, USA.

出版信息

Brain Behav Immun. 2009 Mar;23(3):318-24. doi: 10.1016/j.bbi.2008.09.001. Epub 2008 Sep 12.

DOI:10.1016/j.bbi.2008.09.001
PMID:18822367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2746382/
Abstract

Gene modification technologies play a vital role in the study of biological systems and pathways. Although there is widespread and beneficial use of genetic mouse models, potential shortcomings of gene targeting technology exist, and are not always taken into consideration. Oversights associated with the technology can lead to misinterpretation of results; for example, ablation of a gene of interest can appear to cause an observed phenotype when, in fact, residual embryonic stem cell-derived genetic material in the genetic background or in the area immediately surrounding the ablated gene is actually responsible. The purpose of this review is to remind researchers, regardless of scientific discipline, that the background genetics of a knockout strain can have a profound influence on any observed phenotype. It is important that this issue be appropriately addressed during data collection and interpretation.

摘要

基因编辑技术在生物系统和信号通路的研究中发挥着至关重要的作用。尽管基因工程小鼠模型得到了广泛且有益的应用,但基因靶向技术存在潜在的缺点,且这些缺点并非总是被考虑在内。与该技术相关的疏忽可能导致对结果的错误解读;例如,当实际情况是基因背景中或被敲除基因紧邻区域残留的胚胎干细胞衍生遗传物质导致了观察到的表型时,对感兴趣基因的敲除可能看似导致了该表型。本综述的目的是提醒研究人员,无论其学科领域如何,基因敲除品系的背景遗传学可能会对任何观察到的表型产生深远影响。在数据收集和解读过程中妥善处理这个问题很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7364/2746382/b5859c96601f/nihms104336f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7364/2746382/b5859c96601f/nihms104336f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7364/2746382/b5859c96601f/nihms104336f1.jpg