Hsieh Tzung-Fu
Department of Plant and Microbial Biology, Plants for Human Health Institute, North Carolina State University, 600 Lauteate Way, Suite 1329, Kannapolis, NC, 28081, USA,
Methods Mol Biol. 2015;1284:27-40. doi: 10.1007/978-1-4939-2444-8_2.
In many eukaryotic organisms, methylation at the fifth carbon of cytosine (5mC) is a stable epigenetic mark crucial for many biological processes, including cell differentiation, X-chromosome inactivation, transposon silencing, and genomic imprinting. DNA methylation can be stably inherited to the subsequent generation. It can also change dynamically in response to developmental cues or environmental stimuli, and is an important regulator for developmental switch and cell fate determination. Consequently, many human diseases are associated with aberrant DNA methylation. Gene-specific methylation analysis by sequencing of bisulfite-treated genomic DNA has been instrumental in understanding how DNA methylation affects gene transcription. In recent years, techniques have been developed for genome-wide 5mC detection, and complete methylome at single base resolution has been reported for several organisms, providing unprecedented details on the dynamic nature of DNA methylation during development. With the advance in high-throughput sequencing and the availability of genome sequences, mapping the methylome for species with complex genomes has become increasingly feasible.
在许多真核生物中,胞嘧啶的第五个碳原子上的甲基化(5mC)是一种稳定的表观遗传标记,对许多生物学过程至关重要,包括细胞分化、X染色体失活、转座子沉默和基因组印记。DNA甲基化可以稳定地遗传给后代。它也可以根据发育线索或环境刺激而动态变化,并且是发育开关和细胞命运决定的重要调节因子。因此,许多人类疾病与异常的DNA甲基化有关。通过对亚硫酸氢盐处理的基因组DNA进行测序来进行基因特异性甲基化分析,有助于理解DNA甲基化如何影响基因转录。近年来,已经开发出用于全基因组5mC检测的技术,并且已经报道了几种生物在单碱基分辨率下的完整甲基化组,为发育过程中DNA甲基化的动态性质提供了前所未有的详细信息。随着高通量测序的进展和基因组序列的可用性,绘制复杂基因组物种的甲基化组变得越来越可行。