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综合 FISH 探针设计工具在人免疫球蛋白类别转换重组的成像中的应用。

Comprehensive FISH probe design tool applied to imaging human immunoglobulin class switch recombination.

机构信息

Randall Division of Cell and Molecular Biophysics, King's College London, London, United Kingdom.

出版信息

PLoS One. 2012;7(12):e51675. doi: 10.1371/journal.pone.0051675. Epub 2012 Dec 14.

Abstract

We present a web engine boosted fluorescence in-situ hybridization (webFISH) algorithm using a genome-wide sequence similarity search to design target-specific single-copy and repetitive DNA FISH probes. The webFISH algorithm featuring a user-friendly interface (http://www.webfish2.org/) maximizes the coverage of the examined sequences with FISH probes by considering locally repetitive sequences absent from the remainder of the genome. The highly repetitive human immunoglobulin heavy chain sequence was analyzed using webFISH to design three sets of FISH probes. These allowed direct simultaneous detection of class switch recombination in both immunoglobulin-heavy chain alleles in single cells from a population of cultured primary B cells. It directly demonstrated asynchrony of the class switch recombination in the two alleles in structurally preserved nuclei while permitting parallel readout of protein expression by immunofluorescence staining. This novel technique offers the possibility of gaining unprecedented insight into the molecular mechanisms involved in class switch recombination.

摘要

我们提出了一种基于网络的荧光原位杂交(webFISH)算法,该算法利用全基因组序列相似性搜索来设计针对特定单拷贝和重复 DNA 的 FISH 探针。该 webFISH 算法具有用户友好的界面(http://www.webfish2.org/),通过考虑基因组其余部分中不存在的局部重复序列,最大限度地提高了 FISH 探针对被检测序列的覆盖度。使用 webFISH 分析高度重复的人免疫球蛋白重链序列,设计了三组 FISH 探针。这些探针可直接同时检测来自培养的原代 B 细胞群体中单细胞中两个免疫球蛋白重链等位基因的类别转换重组。它直接证明了在结构保存的核中两个等位基因的类别转换重组的不同步,同时允许通过免疫荧光染色进行并行的蛋白质表达读出。这项新技术提供了一种前所未有的可能性,可以深入了解类别转换重组所涉及的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caab/3522715/f6ece98fa733/pone.0051675.g001.jpg

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