Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, California 21546.
Molecular and Computational Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, California 21546
Genetics. 2015 Oct;201(2):769-77. doi: 10.1534/genetics.115.180661. Epub 2015 Jul 30.
Genetic heterogeneity occurs when individuals express similar phenotypes as a result of different underlying mechanisms. Although such heterogeneity is known to be a potential source of unexplained heritability in genetic mapping studies, its prevalence and molecular basis are not fully understood. Here we show that substantial genetic heterogeneity underlies a model phenotype--the ability to grow invasively--in a cross of two Saccharomyces cerevisiae strains. The heterogeneous basis of this trait across genotypes and environments makes it difficult to detect causal loci with standard genetic mapping techniques. However, using selective genotyping in the original cross, as well as in targeted backcrosses, we detected four loci that contribute to differences in the ability to grow invasively. Identification of causal genes at these loci suggests that they act by changing the underlying regulatory architecture of invasion. We verified this point by deleting many of the known transcriptional activators of invasion, as well as the gene encoding the cell surface protein Flo11 from five relevant segregants and showing that these individuals differ in the genes they require for invasion. Our work illustrates the extensive genetic heterogeneity that can underlie a trait and suggests that regulatory rewiring is a basic mechanism that gives rise to this heterogeneity.
遗传异质性是指个体表现出相似的表型,但其潜在机制却不同。尽管这种异质性是遗传图谱研究中未被解释的遗传率的一个潜在来源,但它的普遍性和分子基础尚未完全了解。在这里,我们展示了在两个酿酒酵母菌株的杂交中,一个模型表型——侵袭性生长的能力——存在着大量的遗传异质性。这种性状在基因型和环境之间的异质性基础使得使用标准遗传图谱技术检测因果基因座变得非常困难。然而,通过在原始杂交以及靶向回交中进行选择性基因分型,我们检测到四个与侵袭性生长能力差异有关的基因座。这些基因座上的因果基因的鉴定表明,它们通过改变侵袭的潜在调节结构起作用。我们通过删除五个相关分离子中许多已知的侵袭性转录激活因子以及编码细胞表面蛋白 Flo11 的基因来验证这一点,并表明这些个体在入侵所需的基因上存在差异。我们的工作说明了可以为一个性状提供基础的遗传异质性的广泛性,并表明调节重布线是产生这种异质性的基本机制。