Center for Plant Biology and Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Helmholtz Pioneer Campus, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Genome Biol Evol. 2022 May 3;14(5). doi: 10.1093/gbe/evac066.
Chromatin remodelers play a fundamental role in the assembly of chromatin, regulation of transcription, and DNA repair. Biochemical and functional characterizations of the CHD family of chromatin remodelers from a variety of model organisms have shown that these remodelers participate in a wide range of activities. However, because the evolutionary history of CHD homologs is unclear, it is difficult to predict which of these activities are broadly conserved and which have evolved more recently in individual eukaryotic lineages. Here, we performed a comprehensive phylogenetic analysis of 8,042 CHD homologs from 1,894 species to create a model for the evolution of this family across eukaryotes with a particular focus on the timing of duplications that gave rise to the diverse copies observed in plants, animals, and fungi. Our analysis confirms that the three major subfamilies of CHD remodelers originated in the eukaryotic last common ancestor, and subsequent losses occurred independently in different lineages. Improved taxon sampling identified several subfamilies of CHD remodelers in plants that were absent or highly divergent in the model plant Arabidopsis thaliana. Whereas the timing of CHD subfamily expansions in vertebrates corresponds to whole genome duplication events, the mechanisms underlying CHD diversification in land plants appear more complicated. Analysis of protein domains reveals that CHD remodeler diversification has been accompanied by distinct transitions in domain architecture, contributing to the functional differences observed between these remodelers. This study demonstrates the importance of proper taxon sampling when studying ancient evolutionary events to prevent misinterpretation of subsequent lineage-specific changes and provides an evolutionary framework for functional and comparative analysis of this critical chromatin remodeler family across eukaryotes.
染色质重塑因子在染色质的组装、转录调控和 DNA 修复中起着至关重要的作用。对多种模式生物的 CHD 家族染色质重塑因子的生化和功能特征的研究表明,这些重塑因子参与了广泛的活动。然而,由于 CHD 同源物的进化历史尚不清楚,因此很难预测这些活动中有哪些是广泛保守的,哪些是在个别真核生物谱系中最近进化而来的。在这里,我们对来自 1894 个物种的 8042 个 CHD 同源物进行了全面的系统发育分析,为这个家族在真核生物中的进化建立了一个模型,特别关注导致植物、动物和真菌中观察到的多样化拷贝的复制的时间。我们的分析证实,CHD 重塑因子的三个主要亚家族起源于真核生物的最后共同祖先,随后的缺失独立发生在不同的谱系中。改进的分类群采样在植物中确定了几个 CHD 重塑因子亚家族,而在模式植物拟南芥中这些亚家族缺失或高度分化。脊椎动物 CHD 亚家族扩张的时间与全基因组复制事件相对应,而陆地植物中 CHD 多样化的机制似乎更为复杂。对蛋白质结构域的分析表明,CHD 重塑因子的多样化伴随着结构域架构的明显转变,这导致了这些重塑因子之间观察到的功能差异。这项研究表明,在研究古代进化事件时,适当的分类群采样对于防止对后续谱系特异性变化的错误解释是很重要的,并为这个关键的染色质重塑因子家族在真核生物中的功能和比较分析提供了一个进化框架。