Al-Salam Ahmad, Irwin David M
Department of Laboratory Medicine and Pathobiology, Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada.
Banting and Best Diabetes Centre, University of Toronto, Toronto, ON, Canada.
BMC Evol Biol. 2017 Jun 23;17(1):148. doi: 10.1186/s12862-017-0994-z.
Insulin receptor substrate (Irs) proteins are essential for insulin signaling as they allow downstream effectors to dock with, and be activated by, the insulin receptor. A family of four Irs proteins have been identified in mice, however the gene for one of these, IRS3, has been pseudogenized in humans. While it is known that the Irs gene family originated in vertebrates, it is not known when it originated and which members are most closely related to each other. A better understanding of the evolution of Irs genes and proteins should provide insight into the regulation of metabolism by insulin.
Multiple genes for Irs proteins were identified in a wide variety of vertebrate species. Phylogenetic and genomic neighborhood analyses indicate that this gene family originated very early in vertebrae evolution. Most Irs genes were duplicated and retained in fish after the fish-specific genome duplication. Irs genes have been lost of various lineages, including Irs3 in primates and birds and Irs1 in most fish. Irs3 and Irs4 experienced an episode of more rapid protein sequence evolution on the ancestral mammalian lineage. Comparisons of the conservation of the proteins sequences among Irs paralogs show that domains involved in binding to the plasma membrane and insulin receptors are most strongly conserved, while divergence has occurred in sequences involved in interacting with downstream effector proteins.
The Irs gene family originated very early in vertebrate evolution, likely through genome duplications, and in parallel with duplications of other components of the insulin signaling pathway, including insulin and the insulin receptor. While the N-terminal sequences of these proteins are conserved among the paralogs, changes in the C-terminal sequences likely allowed changes in biological function.
胰岛素受体底物(Irs)蛋白对于胰岛素信号传导至关重要,因为它们能使下游效应器与胰岛素受体对接并被其激活。在小鼠中已鉴定出一个由四种Irs蛋白组成的家族,然而其中一种蛋白IRS3的基因在人类中已被假基因化。虽然已知Irs基因家族起源于脊椎动物,但尚不清楚其起源时间以及哪些成员彼此关系最为密切。更好地了解Irs基因和蛋白的进化应能为胰岛素对代谢的调节提供深入见解。
在多种脊椎动物物种中鉴定出了多个Irs蛋白基因。系统发育和基因组邻域分析表明,该基因家族在脊椎动物进化的早期就已起源。大多数Irs基因在鱼类特异性基因组复制后在鱼类中发生了复制并得以保留。Irs基因在不同的谱系中丢失,包括灵长类和鸟类中的Irs3以及大多数鱼类中的Irs1。Irs3和Irs4在哺乳动物祖先谱系上经历了一段蛋白质序列进化更快的时期。对Irs旁系同源物之间蛋白质序列保守性的比较表明,与质膜和胰岛素受体结合的结构域保守性最强,而与下游效应器蛋白相互作用的序列则发生了分化。
Irs基因家族在脊椎动物进化的早期就已起源,可能是通过基因组复制,并且与胰岛素信号通路的其他成分(包括胰岛素和胰岛素受体)的复制同时发生。虽然这些蛋白的N端序列在旁系同源物之间是保守的,但C端序列的变化可能导致了生物学功能的改变。