Pervasive evolution of tissue-specificity of ancestral genes differentially shaped vertebrates and insects

Abstract

AbstractRegulation of gene expression is arguably the main mechanism contributing to tissue phenotypic diversity within and between species. Here, we assembled a vast RNA-seq dataset covering twenty bilaterian species and eight tissues, selecting a specular phylogeny that allowed both the combined and parallel investigation of gene expression evolution between vertebrates and insects. We specifically focused on widely conserved ancestral genes, identifying strong cores of pan-bilaterian tissue-differential genes but even larger groups that diverged to define vertebrate and insect tissues. Consistently, systematic inferences of tissue-specificity gains and losses show that nearly half of all ancestral genes have been recruited into tissue-specific transcriptomes. This occurred during both ancient and, especially, recent bilaterian evolution, with numerous gains being associated with the emergence of unique phenotypes. Such pervasive evolution of tissue-specificity was boosted by gene duplication coupled with specialization, including an unappreciated prolonged effect of whole genome duplications during recent vertebrate evolution.