Engler P, Doglio L T, Bozek G, Storb U
Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60637, USA.
Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10763-8. doi: 10.1073/pnas.95.18.10763.
Silencing of chromosomal domains has been described in diverse systems such as position effect variegation in insects, silencing near yeast telomeres, and mammalian X chromosome inactivation. In mammals, silencing is associated with methylation at CpG dinucleotides, but little is known about how methylation patterns are established or altered during development. We previously described a strain-specific modifier locus, Ssm1, that controls the methylation of a complex transgene. In this study we address the questions of the nature of Ssm1's targets and whether its effect extends into adjacent sequences. By examining the inheritance of methylation patterns in a series of mice harboring deletion derivatives of the original transgene, we have identified a discrete segment, derived from the gpt gene of Escherichia coli, that is a major determinant for Ssm1-mediated methylation. Methylation analysis of sequences adjacent to a transgenic target indicates that the influence of this modifier extends into the surrounding chromosome in a strain-dependent fashion. Implications for the mechanism of Ssm1 action are discussed.
染色体结构域的沉默已在多种系统中被描述,如昆虫中的位置效应斑驳、酵母端粒附近的沉默以及哺乳动物的X染色体失活。在哺乳动物中,沉默与CpG二核苷酸的甲基化有关,但对于甲基化模式在发育过程中是如何建立或改变的,人们知之甚少。我们之前描述了一个菌株特异性修饰位点Ssm1,它控制一个复杂转基因的甲基化。在本研究中,我们探讨了Ssm1的靶标的性质问题以及其效应是否延伸到相邻序列。通过检查一系列携带原始转基因缺失衍生物的小鼠中甲基化模式的遗传情况,我们确定了一个源自大肠杆菌gpt基因的离散片段,它是Ssm1介导甲基化的主要决定因素。对转基因靶标相邻序列的甲基化分析表明,这种修饰剂的影响以菌株依赖的方式延伸到周围染色体。文中讨论了Ssm1作用机制的相关意义。