Mantica Federica, Irimia Manuel
Universitat Pompeu Fabra, Barcelona, Spain.
Centre for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Spain.
Bioessays. 2025 May;47(5):e202400202. doi: 10.1002/bies.202400202. Epub 2025 Feb 25.
Animals comprise hundreds of cell types, each with specialized biological functions. However, many genes expressed in each cell type belong to widely conserved gene families with ancestrally ubiquitous expression. This raises a paradox: how have these genes evolved to shape cell type-specific traits without compromising their ancestral function in all other cells? This can be achieved through gene duplication and the origin of regulated, alternatively spliced exons, which generate new related proteins in the form of paralogous genes and alternative isoforms, respectively. Here, we explore how such new related proteins can contribute to the evolution of specific cell types while preserving broader ancestral roles. Specifically, we separately classify possible expression and functional fates for new related proteins and discuss their interplays and evolutionary likelihood. Our primary hypothesis is that expression specialization, mostly coupled with functional specialization, is the predominant fate for both paralogous genes and alternative isoforms throughout animal evolution.
动物包含数百种细胞类型,每种细胞类型都具有特定的生物学功能。然而,每种细胞类型中表达的许多基因都属于广泛保守的基因家族,这些基因在进化史上普遍表达。这就产生了一个悖论:这些基因是如何在不影响其在所有其他细胞中的原始功能的情况下进化,从而塑造特定细胞类型的特征的?这可以通过基因复制以及受调控的可变剪接外显子的产生来实现,可变剪接外显子分别以旁系同源基因和可变异构体的形式产生新的相关蛋白质。在这里,我们探讨这些新的相关蛋白质如何在保留更广泛的原始作用的同时,促进特定细胞类型的进化。具体而言,我们分别对新的相关蛋白质可能的表达和功能命运进行分类,并讨论它们之间的相互作用以及进化可能性。我们的主要假设是,在整个动物进化过程中,表达特化(大多与功能特化相关联)是旁系同源基因和可变异构体的主要命运。