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短串联重复序列的变异介导了拟南芥中的复杂上位性相互作用。

Variability in a Short Tandem Repeat Mediates Complex Epistatic Interactions in Arabidopsis thaliana.

作者信息

Press Maximilian Oliver, Queitsch Christine

机构信息

University of Washington, Department of Genome Sciences, Seattle, Washington 98195.

University of Washington, Department of Genome Sciences, Seattle, Washington 98195

出版信息

Genetics. 2017 Jan;205(1):455-464. doi: 10.1534/genetics.116.193359. Epub 2016 Nov 18.

Abstract

Short tandem repeats (STRs) are hypervariable genetic elements that occur frequently in coding regions. Their high mutation rate readily generates genetic variation, contributing to adaptive evolution and human diseases. We previously reported that natural ELF3 polyglutamine variants cause reciprocal genetic incompatibilities in two divergent Arabidopsis thaliana backgrounds. Here, we dissect the genetic architecture of this incompatibility, revealing as many as four loci putatively interacting with ELF3 We were able to specifically identify one such ELF3-interacting gene, LSH9 We further used a yeast two-hybrid strategy to identify proteins whose physical interactions with ELF3 were affected by polyglutamine tract length. We found two proteins for which this was the case, ELF4 and AtGLDP1. Using these two approaches, we identify specific genetic interactions and physical mechanisms by which the ELF3 polyglutamine tract may mediate the observed genetic incompatibilities. Our work elucidates how STR variation, which is generally underascertained in population-scale sequencing, can contribute to phenotypic variation. Furthermore, our results support our proposal that highly variable STR loci can contribute to the epistatic component of heritability.

摘要

短串联重复序列(STRs)是在编码区频繁出现的高变遗传元件。它们的高突变率很容易产生遗传变异,促进适应性进化和引发人类疾病。我们之前报道过,天然的ELF3多聚谷氨酰胺变体在两种不同的拟南芥背景中会导致相互的遗传不相容性。在这里,我们剖析了这种不相容性的遗传结构,发现多达四个位点可能与ELF3相互作用。我们能够特异性地鉴定出一个这样与ELF3相互作用的基因,即LSH9。我们进一步使用酵母双杂交策略来鉴定其与ELF3的物理相互作用受多聚谷氨酰胺链长度影响的蛋白质。我们发现有两种蛋白质是这种情况,即ELF4和AtGLDP1。通过这两种方法,我们确定了ELF3多聚谷氨酰胺链可能介导所观察到的遗传不相容性的特定遗传相互作用和物理机制。我们的工作阐明了在群体规模测序中通常未被充分确定的STR变异如何能导致表型变异。此外,我们的结果支持了我们的提议,即高度可变的STR位点可对遗传力的上位性成分有所贡献。

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