Giraldo Angelica M, Bondioli Kenneth R
Revivicor, Inc., Blacksburg, VA, USA.
Methods Mol Biol. 2011;791:145-56. doi: 10.1007/978-1-61779-316-5_12.
DNA methylation plays a significant role in the expression of the genetic code and affects early growth and development through its influence on gene expression. DNA methyltransferase 1 (Dnmt1) is the enzyme responsible for maintaining the methylation marks through cell division. However, the de novo methyltransferases, Dnmt3a and Dnmt3b, can also contribute to the maintenance of the methylation pattern. Manipulation of these enzymes, especially Dnmt1, provides a means to alter DNA methylation levels. Manipulation of the DNA methylation pattern of somatic cells will allow a better understanding of the different molecular process associated with chromatin structure and gene expression. Different approaches to artificially manipulate the expression of Dnmt1 in somatic cells include the addition of 5-azacytidine, culture of cells for an extended period of time, and the use of small interfering RNA technologies.
DNA甲基化在遗传密码的表达中起着重要作用,并通过其对基因表达的影响来影响早期生长和发育。DNA甲基转移酶1(Dnmt1)是负责在细胞分裂过程中维持甲基化标记的酶。然而,从头甲基转移酶Dnmt3a和Dnmt3b也有助于维持甲基化模式。对这些酶,尤其是Dnmt1的操控提供了一种改变DNA甲基化水平的方法。对体细胞DNA甲基化模式的操控将有助于更好地理解与染色质结构和基因表达相关的不同分子过程。在体细胞中人工操控Dnmt1表达的不同方法包括添加5-氮杂胞苷、长时间培养细胞以及使用小干扰RNA技术。