Center for Genomics and Systems Biology, Department of Biology, New York University, New York, New York, United States of America.
PLoS Genet. 2013;9(8):e1003733. doi: 10.1371/journal.pgen.1003733. Epub 2013 Aug 22.
Biological systems produce phenotypes that appear to be robust to perturbation by mutations and environmental variation. Prior studies identified genes that, when impaired, reveal previously cryptic genetic variation. This result is typically interpreted as evidence that the disrupted gene normally increases robustness to mutations, as such robustness would allow cryptic variants to accumulate. However, revelation of cryptic genetic variation is not necessarily evidence that a mutationally robust state has been made less robust. Demonstrating a difference in robustness requires comparing the ability of each state (with the gene perturbed or intact) to suppress the effects of new mutations. Previous studies used strains in which the existing genetic variation had been filtered by selection. Here, we use mutation accumulation (MA) lines that have experienced minimal selection, to test the ability of histone H2A.Z (HTZ1) to increase robustness to mutations in the yeast Saccharomyces cerevisiae. HTZ1, a regulator of chromatin structure and gene expression, represents a class of genes implicated in mutational robustness. It had previously been shown to increase robustness of yeast cell morphology to fluctuations in the external or internal microenvironment. We measured morphological variation within and among 79 MA lines with and without HTZ1. Analysis of within-line variation confirms that HTZ1 increases microenvironmental robustness. Analysis of between-line variation shows the morphological effects of eliminating HTZ1 to be highly dependent on the line, which implies that HTZ1 interacts with mutations that have accumulated in the lines. However, lines without HTZ1 are, as a group, not more phenotypically diverse than lines with HTZ1 present. The presence of HTZ1, therefore, does not confer greater robustness to mutations than its absence. Our results provide experimental evidence that revelation of cryptic genetic variation cannot be assumed to be caused by loss of robustness, and therefore force reevaluation of prior claims based on that assumption.
生物系统产生的表型似乎对突变和环境变化具有很强的抗扰能力。先前的研究确定了一些基因,如果这些基因受到损伤,就会揭示先前隐藏的遗传变异。这一结果通常被解释为,被破坏的基因通常会增加对突变的稳健性,因为这种稳健性会允许隐藏的变体积累。然而,揭示隐藏的遗传变异不一定是突变稳健状态变得不那么稳健的证据。要证明稳健性的差异,需要比较每个状态(基因受到干扰或完整)抑制新突变影响的能力。先前的研究使用的是通过选择过滤了现有遗传变异的菌株。在这里,我们使用经历了最小选择的突变积累(MA)系来测试组蛋白 H2A.Z(HTZ1)增加酵母酿酒酵母中突变稳健性的能力。HTZ1 是染色质结构和基因表达的调节剂,代表了一类与突变稳健性相关的基因。它以前被证明可以增加酵母细胞形态对外部或内部微环境波动的稳健性。我们测量了 79 条带有和不带有 HTZ1 的 MA 系内和系间的形态变异。对系内变异的分析证实,HTZ1 增加了微环境的稳健性。对系间变异的分析表明,消除 HTZ1 的形态效应高度依赖于系,这意味着 HTZ1 与在系中积累的突变相互作用。然而,没有 HTZ1 的系作为一个整体并不比有 HTZ1 存在的系表现出更多的表型多样性。因此,HTZ1 的存在并没有赋予比其缺失更大的对突变的稳健性。我们的结果提供了实验证据,表明隐藏遗传变异的揭示不能被假定为稳健性的丧失所导致,因此需要重新评估基于该假设的先前主张。