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超新星:一种用于体内单细胞标记和基因功能研究的多功能载体系统。

Supernova: A Versatile Vector System for Single-Cell Labeling and Gene Function Studies in vivo.

作者信息

Luo Wenshu, Mizuno Hidenobu, Iwata Ryohei, Nakazawa Shingo, Yasuda Kosuke, Itohara Shigeyoshi, Iwasato Takuji

机构信息

Division of Neurogenetics, National Institute of Genetics, Mishima, 411-8540, Japan.

Department of Genetics, SOKENDAI (The Graduate University for Advanced Studies), Mishima, 411-8540, Japan.

出版信息

Sci Rep. 2016 Oct 24;6:35747. doi: 10.1038/srep35747.

DOI:10.1038/srep35747
PMID:27775045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5075795/
Abstract

Here we describe "Supernova" series of vector systems that enable single-cell labeling and labeled cell-specific gene manipulation, when introduced by in utero electroporation (IUE) or adeno-associated virus (AAV)-mediated gene delivery. In Supernova, sparse labeling relies on low TRE leakage. In a small population of cells with over-threshold leakage, initial tTA-independent weak expression is enhanced by tTA/TRE-positive feedback along with a site-specific recombination system (e.g., Cre/loxP, Flpe/FRT). Sparse and bright labeling by Supernova with little background enables the visualization of the morphological details of individual neurons in densely packed brain areas such as the cortex and hippocampus, both during development and in adulthood. Sparseness levels are adjustable. Labeled cell-specific gene knockout was accomplished by introducing Cre/loxP-based Supernova vectors into floxed mice. Furthermore, by combining with RNAi, TALEN, and CRISPR/Cas9 technologies, IUE-based Supernova achieved labeled cell-specific gene knockdown and editing/knockout without requiring genetically altered mice. Thus, Supernova system is highly extensible and widely applicable for single-cell analyses in complex organs, such as the mammalian brain.

摘要

在此,我们描述了“超新星”系列载体系统,当通过子宫内电穿孔(IUE)或腺相关病毒(AAV)介导的基因传递引入时,该系统能够实现单细胞标记和标记细胞特异性基因操作。在超新星系统中,稀疏标记依赖于低TRE泄漏。在一小部分具有超阈值泄漏的细胞中,初始的非tTA依赖性弱表达通过tTA/TRE阳性反馈以及位点特异性重组系统(如Cre/loxP、Flpe/FRT)得到增强。超新星系统实现的稀疏且明亮标记以及低背景,使得在发育过程中和成年期都能够可视化密集排列的脑区(如皮层和海马体)中单个神经元的形态细节。稀疏程度是可调节的。通过将基于Cre/loxP的超新星载体引入floxed小鼠,实现了标记细胞特异性基因敲除。此外,通过与RNAi、TALEN和CRISPR/Cas9技术相结合,基于IUE的超新星系统无需对小鼠进行基因改造即可实现标记细胞特异性基因敲低和编辑/敲除。因此,超新星系统具有高度的可扩展性,广泛适用于复杂器官(如哺乳动物大脑)的单细胞分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/9abffe10f236/srep35747-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/54e5e6c39a82/srep35747-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/7371d012e82c/srep35747-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/76408a94547b/srep35747-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/0c83d38c65ba/srep35747-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/bc5adc83dbe4/srep35747-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/9abffe10f236/srep35747-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/54e5e6c39a82/srep35747-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/7fbfdbd0152f/srep35747-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/eac6855974c8/srep35747-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/7371d012e82c/srep35747-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/76408a94547b/srep35747-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/0c83d38c65ba/srep35747-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/bc5adc83dbe4/srep35747-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbed/5075795/9abffe10f236/srep35747-f8.jpg

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2
A Retroviral CRISPR-Cas9 System for Cellular Autism-Associated Phenotype Discovery in Developing Neurons.一种用于在发育中的神经元中发现细胞自闭症相关表型的逆转录病毒CRISPR-Cas9系统。
Sci Rep. 2016 May 10;6:25611. doi: 10.1038/srep25611.
3
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PLoS One. 2025 Jun 6;20(6):e0321014. doi: 10.1371/journal.pone.0321014. eCollection 2025.
4
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J Neurosci. 2025 May 21;45(21):e0201252025. doi: 10.1523/JNEUROSCI.0201-25.2025.
5
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6
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