Lewis James J, van der Burg Karin R L, Mazo-Vargas Anyi, Reed Robert D
Department of Ecology and Evolutionary Biology, Cornell University, 215 Tower Road, Ithaca, NY 14853-7202, USA.
Department of Ecology and Evolutionary Biology, Cornell University, 215 Tower Road, Ithaca, NY 14853-7202, USA.
Cell Rep. 2016 Sep 13;16(11):2855-2863. doi: 10.1016/j.celrep.2016.08.042.
Uncovering phylogenetic patterns of cis-regulatory evolution remains a fundamental goal for evolutionary and developmental biology. Here, we characterize the evolution of regulatory loci in butterflies and moths using chromatin immunoprecipitation sequencing (ChIP-seq) annotation of regulatory elements across three stages of head development. In the process we provide a high-quality, functionally annotated genome assembly for the butterfly, Heliconius erato. Comparing cis-regulatory element conservation across six lepidopteran genomes, we find that regulatory sequences evolve at a pace similar to that of protein-coding regions. We also observe that elements active at multiple developmental stages are markedly more conserved than elements with stage-specific activity. Surprisingly, we also find that stage-specific proximal and distal regulatory elements evolve at nearly identical rates. Our study provides a benchmark for genome-wide patterns of regulatory element evolution in insects, and it shows that developmental timing of activity strongly predicts patterns of regulatory sequence evolution.
揭示顺式调控进化的系统发育模式仍然是进化生物学和发育生物学的一个基本目标。在这里,我们利用染色质免疫沉淀测序(ChIP-seq)对头发育三个阶段的调控元件进行注释,来表征蝴蝶和蛾类调控位点的进化。在此过程中,我们为红带袖蝶提供了一个高质量、功能注释的基因组组装。比较六个鳞翅目基因组中的顺式调控元件保守性,我们发现调控序列的进化速度与蛋白质编码区域相似。我们还观察到,在多个发育阶段活跃的元件比具有阶段特异性活性的元件明显更保守。令人惊讶的是,我们还发现阶段特异性近端和远端调控元件的进化速度几乎相同。我们的研究为昆虫调控元件进化的全基因组模式提供了一个基准,并且表明活性的发育时间强烈预测调控序列进化的模式。