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使用……在三维染色质重建中整合多分辨率数据

Integration of Multiple Resolution Data in 3D Chromatin Reconstruction Using .

作者信息

Caudai Claudia, Zoppè Monica, Tonazzini Anna, Merelli Ivan, Salerno Emanuele

机构信息

National Research Council of Italy, Institute of Information Science and Technologies, 56124 Pisa, Italy.

National Research Council of Italy, Institute of BioPhysics, 20133 Milano, Italy.

出版信息

Biology (Basel). 2021 Apr 16;10(4):338. doi: 10.3390/biology10040338.

Abstract

The three-dimensional structure of chromatin in the cellular nucleus carries important information that is connected to physiological and pathological correlates and dysfunctional cell behaviour. As direct observation is not feasible at present, on one side, several experimental techniques have been developed to provide information on the spatial organization of the DNA in the cell; on the other side, several computational methods have been developed to elaborate experimental data and infer 3D chromatin conformations. The most relevant experimental methods are Chromosome Conformation Capture and its derivatives, chromatin immunoprecipitation and sequencing techniques (CHIP-seq), RNA-seq, fluorescence in situ hybridization (FISH) and other genetic and biochemical techniques. All of them provide important and complementary information that relate to the three-dimensional organization of chromatin. However, these techniques employ very different experimental protocols and provide information that is not easily integrated, due to different contexts and different resolutions. Here, we present an open-source tool, which is an expansion of the previously reported code , for inferring the 3D structure of chromatin that, by exploiting a multilevel approach, allows an easy integration of information derived from different experimental protocols and referred to different resolution levels of the structure, from a few kilobases up to Megabases. Our results show that the introduction of chromatin modelling features related to CTCF CHIA-PET data, histone modification CHIP-seq, and RNA-seq data produce appreciable improvements in 's 3D reconstructions, compared to the use of HI-C data alone, at a local level and at a very high resolution.

摘要

细胞核中染色质的三维结构携带了与生理和病理相关性以及细胞功能失调行为相关的重要信息。由于目前直接观察不可行,一方面,已经开发了几种实验技术来提供关于细胞中DNA空间组织的信息;另一方面,已经开发了几种计算方法来处理实验数据并推断三维染色质构象。最相关的实验方法是染色体构象捕获及其衍生技术、染色质免疫沉淀和测序技术(CHIP-seq)、RNA测序(RNA-seq)、荧光原位杂交(FISH)以及其他遗传和生化技术。所有这些技术都提供了与染色质三维组织相关的重要且互补的信息。然而,这些技术采用非常不同的实验方案,并且由于不同的背景和分辨率,所提供的信息不易整合。在这里,我们展示了一个开源工具,它是先前报告代码的扩展,用于推断染色质的三维结构,该工具通过采用多级方法,能够轻松整合来自不同实验方案且涉及从几千碱基到兆碱基不同结构分辨率水平的信息。我们的结果表明,与仅使用Hi-C数据相比,引入与CTCF CHIA-PET数据、组蛋白修饰CHIP-seq和RNA-seq数据相关的染色质建模特征,在局部水平和非常高的分辨率下,能使三维重建有显著改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2e1/8072831/c16635e333c4/biology-10-00338-g001.jpg

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