Department of Genetics, Yale School of Medicine, New Haven, CT, USA.
Department of Biology, Genome Biology and Epigenetics, Institute of Biodynamics and Biocomplexity, Utrecht University, Utrecht, The Netherlands.
Mol Biol Evol. 2024 Oct 4;41(10). doi: 10.1093/molbev/msae199.
Transcriptional enhancers orchestrate cell type- and time point-specific gene expression programs. Genetic variation within enhancer sequences is an important contributor to phenotypic variation including evolutionary adaptations and human disease. Certain genes and pathways may be more prone to regulatory evolution than others, with different patterns across diverse organisms, but whether such patterns exist has not been investigated at a sufficient scale. To address this question, we identified signatures of accelerated sequence evolution in conserved enhancer elements throughout the mammalian phylogeny at an unprecedented scale. While different genes and pathways were enriched for regulatory evolution in different parts of the tree, we found a striking overall pattern of pleiotropic genes involved in gene regulatory and developmental processes being enriched for accelerated enhancer evolution. These genes were connected to more enhancers than other genes, which was the basis for having an increased amount of sequence acceleration over all their enhancers combined. We provide evidence that sequence acceleration is associated with turnover of regulatory function. Detailed study of one acceleration event in an enhancer of HES1 revealed that sequence evolution led to a new activity domain in the developing limb that emerged concurrently with the evolution of digit reduction in hoofed mammals. Our results provide evidence that enhancer evolution has been a frequent contributor to regulatory innovation at conserved developmental signaling genes in mammals.
转录增强子协调细胞类型和时间点特异性的基因表达程序。增强子序列中的遗传变异是表型变异的一个重要贡献因素,包括进化适应和人类疾病。某些基因和途径可能比其他基因和途径更容易受到调控进化的影响,在不同的生物体中呈现出不同的模式,但这种模式是否存在尚未在足够的规模上进行研究。为了解决这个问题,我们在哺乳动物系统发育的整个范围内,以前所未有的规模确定了保守增强子元件中加速序列进化的特征。虽然不同的基因和途径在树的不同部分富集了调控进化,但我们发现了一个惊人的总体模式,即参与基因调控和发育过程的多效基因富集了加速增强子进化。这些基因与其他基因相比,与更多的增强子相连,这是它们所有增强子组合中序列加速增加的基础。我们提供的证据表明,序列加速与调控功能的转换有关。对 HES1 增强子中一个加速事件的详细研究表明,序列进化导致了发育中的肢体出现新的活性域,同时也伴随着有蹄哺乳动物的趾数减少的进化。我们的研究结果提供了证据,表明增强子进化一直是哺乳动物保守发育信号基因调控创新的一个常见贡献因素。