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A cis-acting element that directs the activity of the murine methylation modifier locus Ssm1

机译:顺式作用元件,指导鼠甲基化修饰位点Ssm1的活性

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摘要

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.
机译:已经在多种系统中描述了染色体结构域的沉默,例如昆虫中的位置效应变异,酵母端粒附近的沉默以及哺乳动物X染色体失活。在哺乳动物中,沉默与CpG二核苷酸处的甲基化有关,但是人们对在发育过程中如何建立或改变甲基化模式知之甚少。我们先前描述了一种应变特异性修饰位点Ssm1,它控制复杂转基因的甲基化。在这项研究中,我们解决了Ssm1靶标的性质及其作用是否扩展到相邻序列的问题。通过检查一系列具有原始转基因缺失衍生物的小鼠中甲基化模式的遗传,我们确定了一个离散片段,该片段衍生自大肠杆菌的gpt基因,是Ssm1介导的甲基化的主要决定因素。对与转基因靶标相邻的序列进行甲基化分析表明,该修饰子的影响以应变依赖的方式延伸到周围的染色体中。讨论了对Ssm1作用机制的影响。

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