Department of Microbiology and Immunology and Department of Biochemistry and Biophysics, University of California, San Francisco, California 94158, USA.
Nature. 2010 Dec 16;468(7326):959-63. doi: 10.1038/nature09560.
Changes in gene regulatory networks are a major source of evolutionary novelty. Here we describe a specific type of network rewiring event, one that intercalates a new level of transcriptional control into an ancient circuit. We deduce that, over evolutionary time, the direct ancestral connections between a regulator and its target genes were broken and replaced by indirect connections, preserving the overall logic of the ancestral circuit but producing a new behaviour. The example was uncovered through a series of experiments in three ascomycete yeasts: the bakers' yeast Saccharomyces cerevisiae, the dairy yeast Kluyveromyces lactis and the human pathogen Candida albicans. All three species have three cell types: two mating-competent cell forms (a and α) and the product of their mating (a/α), which is mating-incompetent. In the ancestral mating circuit, two homeodomain proteins, Mata1 and Matα2, form a heterodimer that directly represses four genes that are expressed only in a and α cells and are required for mating. In a relatively recent ancestor of K. lactis, a reorganization occurred. The Mata1-Matα2 heterodimer represses the same four genes (known as the core haploid-specific genes) but now does so indirectly through an intermediate regulatory protein, Rme1. The overall logic of the ancestral circuit is preserved (haploid-specific genes ON in a and α cells and OFF in a/α cells), but a new phenotype was produced by the rewiring: unlike S. cerevisiae and C. albicans, K. lactis integrates nutritional signals, by means of Rme1, into the decision of whether or not to mate.
基因调控网络的变化是进化新颖性的主要来源。在这里,我们描述了一种特定类型的网络重布线事件,即一种将新的转录控制水平插入古老电路的事件。我们推断,在进化过程中,调节因子与其靶基因之间的直接祖先连接被打破,并被间接连接所取代,保留了祖先电路的整体逻辑,但产生了新的行为。这个例子是通过在三种子囊菌酵母中进行的一系列实验发现的:面包酵母酿酒酵母、乳酵母克鲁维酵母和人类病原体白色念珠菌。这三个物种都有三种细胞类型:两种有性能力的细胞形式(a 和 α)和它们交配的产物(a/α),它是没有交配能力的。在祖先的交配电路中,两个同源域蛋白 Mata1 和 Matα2 形成异二聚体,直接抑制仅在 a 和 α 细胞中表达的四个基因,这些基因是交配所必需的。在 K. lactis 的一个相对较近的祖先中,发生了重组。Mata1-Matα2 异二聚体抑制相同的四个基因(称为核心单倍体特异性基因),但现在通过中间调节蛋白 Rme1 间接进行。祖先电路的整体逻辑得以保留(单倍体特异性基因在 a 和 α 细胞中开启,在 a/α 细胞中关闭),但通过重新布线产生了新的表型:与 S. cerevisiae 和 C. albicans 不同,K. lactis 通过 Rme1 将营养信号整合到是否交配的决策中。