Storb U, Arp B
Proc Natl Acad Sci U S A. 1983 Nov;80(21):6642-6. doi: 10.1073/pnas.80.21.6642.
Different states of eukaryotic gene expression are often correlated with different levels of methylation of DNA sequences containing structural genes and their flanking regions. To assess the potential role of DNA methylation in the expression of immunoglobulin genes, which require complex rearrangements prior to expression, methylation patterns were examined in cell lines representing different stages of lymphocyte maturation. Methylation of the second cytosine in the sequence 5' C-C-G-G 3' was determined by using Hpa II/Msp I endonuclease digestion. Four CH genes (C mu, C delta, C gamma 2b, and C alpha), C kappa, V kappa, C lambda, and V lambda genes were analyzed. The results lead to the following conclusions: (i) transcribed immunoglobulin genes are undermethylated; (ii) the C gene allelic to an expressed C gene is always also undermethylated; and (iii) all immunoglobulin loci tend to become increasingly undermethylated as B cells mature.
真核基因表达的不同状态通常与包含结构基因及其侧翼区域的DNA序列的不同甲基化水平相关。为了评估DNA甲基化在免疫球蛋白基因表达中的潜在作用,免疫球蛋白基因在表达前需要复杂的重排,研究人员在代表淋巴细胞成熟不同阶段的细胞系中检测了甲基化模式。通过使用Hpa II/Msp I核酸内切酶消化来确定序列5' C-C-G-G 3'中第二个胞嘧啶的甲基化情况。分析了四个CH基因(Cμ、Cδ、Cγ2b和Cα)、Cκ、Vκ、Cλ和Vλ基因。结果得出以下结论:(i)转录的免疫球蛋白基因甲基化不足;(ii)与表达的C基因等位的C基因也总是甲基化不足;(iii)随着B细胞成熟,所有免疫球蛋白基因座往往甲基化程度越来越低。