转录因子和染色质修饰的高通量分析方法:低输入、单细胞和空间基因组技术

IF 2.1 4区 医学 Q3 HEMATOLOGY Blood Cells Molecules and Diseases Pub Date : 2023-07-01 DOI:10.1016/j.bcmd.2023.102745
Mohammad Salma , Charlotte Andrieu-Soler , Virginie Deleuze , Eric Soler
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引用次数: 2

摘要

转录因子和表观基因组特征的全基因组分析有助于阐明DNA模板调控过程,如转录、细胞分化或监测细胞对环境线索的反应。二十年的技术发展导致了一套丰富的方法,逐渐将表观遗传学分析的极限推向单细胞。最近,利用创新生物化学的颠覆性技术开始发挥作用。诸如CUT&;RUN,CUT&;标签及其变体显示出从单个实验和在天然条件下并行调查多种TF或组蛋白修饰的相当大的潜力。这些方法正在成为全基因组分析TF和染色质修饰的主要方法,用于批量、单细胞和空间基因组应用。讨论了这些原则及其利弊。
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High-throughput methods for the analysis of transcription factors and chromatin modifications: Low input, single cell and spatial genomic technologies

Genome-wide analysis of transcription factors and epigenomic features is instrumental to shed light on DNA-templated regulatory processes such as transcription, cellular differentiation or to monitor cellular responses to environmental cues. Two decades of technological developments have led to a rich set of approaches progressively pushing the limits of epigenetic profiling towards single cells. More recently, disruptive technologies using innovative biochemistry came into play. Assays such as CUT&RUN, CUT&Tag and variations thereof show considerable potential to survey multiple TFs or histone modifications in parallel from a single experiment and in native conditions. These are in the path to become the dominant assays for genome-wide analysis of TFs and chromatin modifications in bulk, single-cell, and spatial genomic applications. The principles together with pros and cons are discussed.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
42
审稿时长
14 days
期刊介绍: Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.
期刊最新文献
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