Hellmann-Blumberg U, Hintz M F, Gatewood J M, Schmid C W
Department of Chemistry, University of California, Davis 95616.
Mol Cell Biol. 1993 Aug;13(8):4523-30. doi: 10.1128/mcb.13.8.4523-4530.1993.
Alu repeats are especially rich in CpG dinucleotides, the principal target sites for DNA methylation in eukaryotes. The methylation state of Alus in different human tissues is investigated by simple, direct genomic blot analysis exploiting recent theoretical and practical advances concerning Alu sequence evolution. Whereas Alus are almost completely methylated in somatic tissues such as spleen, they are hypomethylated in the male germ line and tissues which depend on the differential expression of the paternal genome complement for development. In particular, we have identified a subset enriched in young Alus whose CpGs appear to be almost completely unmethylated in sperm DNA. The existence of this subset potentially explains the conservation of CpG dinucleotides in active Alu source genes. These profound, sequence-specific developmental changes in the methylation state of Alu repeats suggest a function for Alu sequences at the DNA level, such as a role in genomic imprinting.
Alu重复序列富含CpG二核苷酸,而CpG二核苷酸是真核生物中DNA甲基化的主要靶位点。利用有关Alu序列进化的最新理论和实践进展,通过简单、直接的基因组印迹分析研究了不同人类组织中Alu的甲基化状态。Alu在诸如脾脏等体细胞组织中几乎完全甲基化,而在雄性生殖系和依赖父本基因组互补体差异表达进行发育的组织中则发生低甲基化。特别是,我们鉴定出了一个富含年轻Alu的亚群,其CpG在精子DNA中似乎几乎完全未甲基化。该亚群的存在可能解释了活性Alu源基因中CpG二核苷酸的保守性。Alu重复序列甲基化状态的这些深刻的、序列特异性的发育变化表明Alu序列在DNA水平上具有某种功能,例如在基因组印记中发挥作用。