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基于微孔板的联合染色质和 DNA 甲基化免疫沉淀检测平台。

Microplate-based platform for combined chromatin and DNA methylation immunoprecipitation assays.

机构信息

UW Medicine Lake Union, University of Washington, Seattle, WA 98109, USA.

出版信息

BMC Mol Biol. 2011 Nov 18;12:49. doi: 10.1186/1471-2199-12-49.

Abstract

BACKGROUND

The processes that compose expression of a given gene are far more complex than previously thought presenting unprecedented conceptual and mechanistic challenges that require development of new tools. Chromatin structure, which is regulated by DNA methylation and histone modification, is at the center of gene regulation. Immunoprecipitations of chromatin (ChIP) and methylated DNA (MeDIP) represent a major achievement in this area that allow researchers to probe chromatin modifications as well as specific protein-DNA interactions in vivo and to estimate the density of proteins at specific sites genome-wide. Although a critical component of chromatin structure, DNA methylation has often been studied independently of other chromatin events and transcription.

RESULTS

To allow simultaneous measurements of DNA methylation with other genomic processes, we developed and validated a simple and easy-to-use high throughput microplate-based platform for analysis of DNA methylation. Compared to the traditional beads-based MeDIP the microplate MeDIP was more sensitive and had lower non-specific binding. We integrated the MeDIP method with a microplate ChIP assay which allows measurements of both DNA methylation and histone marks at the same time, Matrix ChIP-MeDIP platform. We illustrated several applications of this platform to relate DNA methylation, with chromatin and transcription events at selected genes in cultured cells, human cancer and in a model of diabetic kidney disease.

CONCLUSION

The high throughput capacity of Matrix ChIP-MeDIP to profile tens and potentially hundreds of different genomic events at the same time as DNA methylation represents a powerful platform to explore complex genomic mechanism at selected genes in cultured cells and in whole tissues. In this regard, Matrix ChIP-MeDIP should be useful to complement genome-wide studies where the rich chromatin and transcription database resources provide fruitful foundation to pursue mechanistic, functional and diagnostic information at genes of interest in health and disease.

摘要

背景

构成特定基因表达的过程远比之前认为的要复杂得多,这带来了前所未有的概念和机制挑战,需要开发新的工具。染色质结构受 DNA 甲基化和组蛋白修饰的调控,是基因调控的核心。染色质免疫沉淀(ChIP)和甲基化 DNA 免疫沉淀(MeDIP)是该领域的一项重大成就,使研究人员能够在体内探测染色质修饰以及特定蛋白质-DNA 相互作用,并估计特定基因组位点的蛋白质密度。尽管 DNA 甲基化是染色质结构的关键组成部分,但它通常与其他染色质事件和转录独立研究。

结果

为了允许同时测量 DNA 甲基化与其他基因组过程,我们开发并验证了一种简单易用的高通量基于微孔板的平台,用于分析 DNA 甲基化。与传统的基于珠子的 MeDIP 相比,微孔板 MeDIP 更灵敏,非特异性结合更低。我们将 MeDIP 方法与微孔板 ChIP 测定法相结合,该方法允许同时测量 DNA 甲基化和组蛋白标记,即 Matrix ChIP-MeDIP 平台。我们展示了该平台的几种应用,以将 DNA 甲基化与培养细胞、人类癌症和糖尿病肾病模型中选定基因的染色质和转录事件联系起来。

结论

Matrix ChIP-MeDIP 高通量的能力可以同时分析数十种甚至数百种不同的基因组事件,同时分析 DNA 甲基化,这代表了一个强大的平台,可以在培养细胞和整个组织中探索选定基因的复杂基因组机制。在这方面,Matrix ChIP-MeDIP 应该有助于补充全基因组研究,其中丰富的染色质和转录数据库资源为在健康和疾病相关基因中追求机制、功能和诊断信息提供了富有成效的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee1e/3247195/969e56cab7f0/1471-2199-12-49-1.jpg

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