Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853
Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853.
Genetics. 2017 Nov;207(3):1157-1166. doi: 10.1534/genetics.117.300306. Epub 2017 Sep 20.
Changes in chromatin state may drive changes in gene expression, and it is of growing interest to understand the population genetic forces that drive differences in chromatin state. Here, we use the phenomenon of position effect variegation (PEV), a well-studied proxy for chromatin state, to survey variation in PEV among a naturally derived population. Further, we explore the genetic architecture of natural variation in factors that modify PEV. While previous mutation screens have identified over 150 suppressors and enhancers of PEV, it remains unknown to what extent allelic variation in these modifiers mediate interindividual variation in PEV. Is natural variation in PEV mediated by segregating genetic variation in known Su(var) and E(var) genes, or is the trait polygenic, with many variants mapping elsewhere in the genome? We designed a dominant mapping study that directly answers this question and suggests that the bulk of the variance in PEV does not map to genes with prior annotated impact to PEV. Instead, we find enrichment of top -value ranked associations that suggest impact to active promoter and transcription start site proximal regions. This work highlights extensive variation in PEV within a population, and provides a quantitative view of the role naturally segregating autosomal variants play in modifying PEV-a phenomenon that continues to shape our understanding of chromatin state and epigenetics.
染色质状态的变化可能导致基因表达的变化,因此越来越有兴趣了解驱动染色质状态差异的群体遗传力。在这里,我们使用位置效应变异 (PEV) 现象作为染色质状态的一个很好的替代指标,来调查自然衍生群体中 PEV 的变化。此外,我们还探讨了影响 PEV 的因素的自然变异的遗传结构。虽然之前的突变筛选已经确定了超过 150 个抑制和增强 PEV 的抑制子和增强子,但这些修饰因子的等位变异在多大程度上介导了 PEV 的个体间差异仍不清楚。PEV 的自然变异是由已知 Su(var)和 E(var)基因的分离遗传变异介导的,还是由许多其他基因座的多基因变异介导的,这些基因座的变异映射到其他地方?我们设计了一个显性图谱研究,直接回答了这个问题,并表明 PEV 的大部分变异都不能映射到先前被注释为影响 PEV 的基因上。相反,我们发现了排名靠前的关联的富集,这表明它们对活性启动子和转录起始位点近端区域有影响。这项工作突出了人群中 PEV 的广泛变化,并提供了对自然分离的常染色体变异在修饰 PEV 中所起作用的定量观点——这一现象继续影响我们对染色质状态和表观遗传学的理解。