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联合使用 3D DNA FISH、单分子 RNA FISH 和免疫荧光技术。

Combined 3D DNA FISH, Single-Molecule RNA FISH, and Immunofluorescence.

机构信息

Tata Institute of Fundamental Research Hyderabad, Hyderabad, Telangana, India.

Ann Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Methods Mol Biol. 2024;2784:203-214. doi: 10.1007/978-1-0716-3766-1_14.

Abstract

Nuclear architecture is a potential regulator of gene expression in eukaryotic cells. Studies connecting nuclear architecture to gene expression are often population-averaged and do not report on the cell-level heterogeneity in genome organization and associated gene expression. In this report we present a simple way to combine fluorescence in situ hybridization (FISH)-based detection of DNA, with single-molecule RNA FISH (smFISH) and immunofluorescence (IF), while also preserving the three-dimensional (3D) nuclear architecture of a cell. Recently developed smFISH techniques enable the detection of individual RNA molecules; while using 3D DNA FISH, copy numbers and positions of genes inside the nucleus can be interrogated without interfering with 3D nuclear architecture. Our method to combine 3D DNA FISH with smFISH and IF enables a unique quantitative handle on the central dogma of molecular biology.

摘要

核架构是真核细胞基因表达的潜在调控因子。将核架构与基因表达联系起来的研究通常是对人群进行平均处理,而没有报告基因组组织和相关基因表达的细胞水平异质性。在本报告中,我们提出了一种简单的方法,可以将基于荧光原位杂交(FISH)的 DNA 检测与单分子 RNA FISH(smFISH)和免疫荧光(IF)结合起来,同时保持细胞的三维(3D)核架构。最近开发的 smFISH 技术能够检测单个 RNA 分子;而使用 3D DNA FISH,可以在不干扰 3D 核架构的情况下,对细胞核内基因的拷贝数和位置进行询问。我们将 3D DNA FISH 与 smFISH 和 IF 相结合的方法,为分子生物学的中心法则提供了一个独特的定量处理方法。

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