Suppr超能文献

化学酶荧光标记基因组 DNA 用于同时检测全基因组 5-甲基胞嘧啶和 5-羟甲基胞嘧啶。

Chemo-Enzymatic Fluorescence Labeling Of Genomic DNA For Simultaneous Detection Of Global 5-Methylcytosine And 5-Hydroxymethylcytosine.

机构信息

Department of Chemistry, Raymond and Beverly SacklerFaculty of Exact Sciences, Department of Biomedical Engineering, Tel Aviv University Tel Aviv-Yafo, 6997801, Tel Aviv, Israel.

School of Chemistry,Ramat Aviv, Tel Aviv University, Tel Aviv, 6997801, Israel.

出版信息

Chembiochem. 2023 Oct 17;24(20):e202300400. doi: 10.1002/cbic.202300400. Epub 2023 Sep 4.

Abstract

5-Methylcytosine and 5-hydroxymethylcytosine are epigenetic modifications involved in gene regulation and cancer. We present a new, simple, and high-throughput platform for multi-color epigenetic analysis. The novelty of our approach is the ability to multiplex methylation and de-methylation signals in the same assay. We utilize an engineered methyltransferase enzyme that recognizes and labels all unmodified CpG sites with a fluorescent cofactor. In combination with the already established labeling of the de-methylation mark 5-hydroxymethylcytosine via enzymatic glycosylation, we obtained a robust platform for simultaneous epigenetic analysis of these marks. We assessed the global epigenetic levels in multiple samples of colorectal cancer and observed a 3.5-fold reduction in 5hmC levels but no change in DNA methylation levels between sick and healthy individuals. We also measured epigenetic modifications in chronic lymphocytic leukemia and observed a decrease in both modification levels (5-hydroxymethylcytosine: whole blood 30 %; peripheral blood mononuclear cells (PBMCs) 40 %. 5-methylcytosine: whole blood 53 %; PBMCs 48 %). Our findings propose using a simple blood test as a viable method for analysis, simplifying sample handling in diagnostics. Importantly, our results highlight the assay's potential for epigenetic evaluation of clinical samples, benefiting research and patient management.

摘要

5-甲基胞嘧啶和 5-羟甲基胞嘧啶是参与基因调控和癌症的表观遗传修饰。我们提出了一种新的、简单的、高通量的多色表观遗传分析平台。我们方法的新颖之处在于能够在同一测定中多路复用甲基化和去甲基化信号。我们利用一种经过工程改造的甲基转移酶,该酶能够识别并标记所有未修饰的 CpG 位点与荧光辅因子。结合已经建立的通过酶糖基化标记去甲基化标记 5-羟甲基胞嘧啶,我们获得了一个同时分析这些标记物的强大平台。我们评估了多个结直肠癌样本的全基因组表观遗传水平,发现 5hmC 水平降低了 3.5 倍,但患病和健康个体之间的 DNA 甲基化水平没有变化。我们还测量了慢性淋巴细胞白血病中的表观遗传修饰,发现两种修饰水平均降低(5-羟甲基胞嘧啶:全血 30%;外周血单核细胞(PBMCs)40%。5-甲基胞嘧啶:全血 53%;PBMCs 48%)。我们的研究结果表明,使用简单的血液测试作为可行的分析方法,可以简化诊断中的样本处理。重要的是,我们的结果强调了该测定法在临床样本表观遗传学评估中的潜在应用,有利于研究和患者管理。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验