• 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

良好的规划和机缘巧合:在睾丸中利用 Cre/Lox 系统。

Good planning and serendipity: exploiting the Cre/Lox system in the testis.

机构信息

MRC Human Reproductive Sciences Unit, The Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.

出版信息

Reproduction. 2011 Feb;141(2):151-61. doi: 10.1530/REP-10-0404. Epub 2010 Nov 17.

DOI:10.1530/REP-10-0404
PMID:21084571
Abstract

Over the past 20 years, genetic manipulation has revolutionised our understanding of male reproductive development and function. The advent of transgenic mouse lines has permitted elegant dissection of previously intractable issues. The development of the Cre/Lox system, which has permitted spatial and temporal localisation of genetic manipulation, has expanded upon this, and now makes up one of the primary approaches underpinning our increasing understanding of testis development and function. The success of conditional gene targeting is largely reliant upon the choice of Cre recombinase expressing mouse line, which is required to specifically target the correct cell type at the correct time. Presupposition that Cre lines will behave as expected has been one of the main oversights in the design of Cre/Lox experiments, as in practice, many Cre lines are prone to ectopic expression (both temporal and spatial), transgene silencing or genetic background effects. Empirical validation of the spatiotemporal profile of Cre expression prior to undertaking conditional gene targeting studies is essential and can be achieved through a combination of molecular and immunohistochemical approaches, along with in vivo examination of reporter gene expression in targeted tissues. This paper details the key considerations associated with exploitation of the Cre/Lox system and highlights a variety of validated Cre lines that have utility for conditional gene targeting within the testis.

摘要

在过去的 20 年中,遗传操作极大地改变了我们对男性生殖发育和功能的理解。转基因小鼠系的出现使以前难以解决的问题得以优雅地解析。Cre/Lox 系统的出现进一步扩展了这一领域,该系统允许在时空上对遗传操作进行定位,现在已成为我们对睾丸发育和功能的日益深入理解的主要方法之一。条件性基因靶向的成功在很大程度上依赖于表达 Cre 重组酶的小鼠系的选择,该选择需要在正确的时间特异性地靶向正确的细胞类型。Cre 系将按照预期表现的假设是 Cre/Lox 实验设计中的主要疏忽之一,因为实际上,许多 Cre 系容易发生异位表达(时空)、转基因沉默或遗传背景效应。在进行条件性基因靶向研究之前,对 Cre 表达的时空特征进行经验验证至关重要,这可以通过分子和免疫组织化学方法的组合以及在靶向组织中对报告基因表达的体内检查来实现。本文详细介绍了利用 Cre/Lox 系统的关键注意事项,并强调了各种经过验证的 Cre 系,它们可用于睾丸内的条件性基因靶向。

相似文献

1
Good planning and serendipity: exploiting the Cre/Lox system in the testis.良好的规划和机缘巧合:在睾丸中利用 Cre/Lox 系统。
Reproduction. 2011 Feb;141(2):151-61. doi: 10.1530/REP-10-0404. Epub 2010 Nov 17.
2
Metabolic pitfalls of CNS Cre-based technology.中枢神经系统 Cre 基因敲入技术的代谢陷阱。
Cell Metab. 2013 Jul 2;18(1):21-8. doi: 10.1016/j.cmet.2013.05.019.
3
Incomplete cre-mediated excision leads to phenotypic differences between Stra8-iCre; Mov10l1(lox/lox) and Stra8-iCre; Mov10l1(lox/Δ) mice.Cre介导的不完全切除导致Stra8-iCre; Mov10l1(lox/lox)和Stra8-iCre; Mov10l1(lox/Δ)小鼠之间的表型差异。
Genesis. 2013 Jul;51(7):481-90. doi: 10.1002/dvg.22389. Epub 2013 Mar 30.
4
Cre-mediated recombination efficiency and transgene expression patterns of three retinal bipolar cell-expressing Cre transgenic mouse lines.三种表达视网膜双极细胞的Cre转基因小鼠品系的Cre介导的重组效率和转基因表达模式。
Mol Vis. 2013 Jun 12;19:1310-20. Print 2013.
5
Temporal and tight hepatitis C virus gene activation in cultured human hepatoma cells mediated by a cell-permeable Cre recombinase.由细胞可渗透的Cre重组酶介导的培养人肝癌细胞中丙型肝炎病毒基因的瞬时和紧密激活。
Acta Biochim Biophys Sin (Shanghai). 2004 Oct;36(10):687-94. doi: 10.1093/abbs/36.10.687.
6
Cre/lox-regulated transgenic zebrafish model with conditional myc-induced T cell acute lymphoblastic leukemia.具有条件性myc诱导的T细胞急性淋巴细胞白血病的Cre/lox调控转基因斑马鱼模型
Proc Natl Acad Sci U S A. 2005 Apr 26;102(17):6068-73. doi: 10.1073/pnas.0408708102. Epub 2005 Apr 12.
7
Pancreas-specific Cre driver lines and considerations for their prudent use.胰腺特异性 Cre 驱动系及其谨慎使用的注意事项。
Cell Metab. 2013 Jul 2;18(1):9-20. doi: 10.1016/j.cmet.2013.06.011.
8
Mouse opsin promoter-directed Cre recombinase expression in transgenic mice.转基因小鼠中鼠视蛋白启动子驱动的Cre重组酶表达。
Mol Vis. 2006 Apr 18;12:389-98.
9
Adenoviral-mediated Cre expression effectively suppresses GlyT1 binding in the thalamic area of GlyT1 conditional knock-out mice.腺病毒介导的 Cre 表达可有效抑制 GlyT1 条件性敲除小鼠丘脑区域 GlyT1 的结合。
J Neurosci Methods. 2010 Nov 30;193(2):254-63. doi: 10.1016/j.jneumeth.2010.09.001. Epub 2010 Sep 9.
10
Temporal control of Cre recombinase-mediated in vitro DNA recombination by Tet-on gene expression system.通过Tet-on基因表达系统对Cre重组酶介导的体外DNA重组进行时间控制。
Acta Biochim Biophys Sin (Shanghai). 2005 Feb;37(2):133-8.

引用本文的文献

1
Cre Deleter Mouse Lines for Conditional Knockout of Genes in Testis Cell Types.用于睾丸细胞类型中基因条件性敲除的Cre删除小鼠品系。
Methods Mol Biol. 2025;2954:287-294. doi: 10.1007/978-1-0716-4698-4_17.
2
Targeted gene silencing in mouse testicular Sertoli and Leydig cells using adeno-associated virus vectors.使用腺相关病毒载体在小鼠睾丸支持细胞和间质细胞中进行靶向基因沉默。
Asian J Androl. 2025 Sep 1;27(5):627-637. doi: 10.4103/aja2024120. Epub 2025 Mar 21.
3
Endothelial cell-specific postnatal deletion of Nos3 preserves intraocular pressure homeostasis via macrophage recruitment and NOS2 upregulation.
出生后内皮细胞特异性缺失Nos3可通过巨噬细胞募集和NOS2上调维持眼内压稳态。
J Clin Invest. 2025 Feb 11;135(7):e183440. doi: 10.1172/JCI183440.
4
A New Leydig Cell-Exclusive Cre Line Allows Lineage Tracing of Fetal and Adult Leydig Cell Populations in the Mouse.一种新的仅在睾丸间质细胞表达的Cre品系可用于对小鼠胎儿和成体睾丸间质细胞群体进行谱系追踪。
Endocrinology. 2025 Jan 6;166(2). doi: 10.1210/endocr/bqaf012.
5
Unlocking Genetic Mysteries during the Epic Sperm Journey toward Fertilization: Further Expanding Mouse Lines.在史诗般的精子向受精旅程中解开遗传之谜:进一步扩展小鼠品系。
Biomolecules. 2024 Apr 28;14(5):529. doi: 10.3390/biom14050529.
6
Generation of a novel Stra8-driven Cre recombinase strain for use in pre-meiotic germ cells in mice†.生成一种新型 Stra8 驱动的 Cre 重组酶菌株,用于小鼠减数分裂前生殖细胞。
Biol Reprod. 2023 Aug 10;109(2):184-191. doi: 10.1093/biolre/ioad063.
7
Generation and Characterization of a Transgenic Mouse That Specifically Expresses the Cre Recombinase in Spermatids.生成并鉴定一种在精细胞中特异性表达 Cre 重组酶的转基因小鼠。
Genes (Basel). 2023 Apr 27;14(5):983. doi: 10.3390/genes14050983.
8
Loss of the repressor REST affects progesterone receptor function and promotes uterine leiomyoma pathogenesis.抑制因子 REST 的缺失会影响孕激素受体的功能,并促进子宫平滑肌瘤的发病机制。
Proc Natl Acad Sci U S A. 2022 Nov;119(44):e2205524119. doi: 10.1073/pnas.2205524119. Epub 2022 Oct 25.
9
Post-transcriptional regulation in spermatogenesis: all RNA pathways lead to healthy sperm.精子发生中的转录后调控:所有 RNA 途径都通向健康的精子。
Cell Mol Life Sci. 2021 Dec;78(24):8049-8071. doi: 10.1007/s00018-021-04012-4. Epub 2021 Nov 8.
10
Connexin43 in Germ Cells Seems to Be Dispensable for Murine Spermatogenesis.缝隙连接蛋白 43 在生殖细胞中似乎对小鼠精子发生不是必需的。
Int J Mol Sci. 2021 Jul 25;22(15):7924. doi: 10.3390/ijms22157924.