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Evolutionary Conservation and Diversification of Puf RNA Binding Proteins and Their mRNA Targets

机译:Puf RNA结合蛋白及其mRNA靶标的进化保守和多样性

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摘要

Reprogramming of a gene’s expression pattern by acquisition and loss of sequences recognized by specific regulatory RNA binding proteins may be a major mechanism in the evolution of biological regulatory programs. We identified that RNA targets of Puf3 orthologs have been conserved over 100–500 million years of evolution in five eukaryotic lineages. Focusing on Puf proteins and their targets across 80 fungi, we constructed a parsimonious model for their evolutionary history. This model entails extensive and coordinated changes in the Puf targets as well as changes in the number of Puf genes and alterations of RNA binding specificity including that: 1) Binding of Puf3 to more than 200 RNAs whose protein products are predominantly involved in the production and organization of mitochondrial complexes predates the origin of budding yeasts and filamentous fungi and was maintained for 500 million years, throughout the evolution of budding yeast. 2) In filamentous fungi, remarkably, more than 150 of the ancestral Puf3 targets were gained by Puf4, with one lineage maintaining both Puf3 and Puf4 as regulators and a sister lineage losing Puf3 as a regulator of these RNAs. The decrease in gene expression of these mRNAs upon deletion of Puf4 in filamentous fungi (N. crassa) in contrast to the increase upon Puf3 deletion in budding yeast (S. cerevisiae) suggests that the output of the RNA regulatory network is different with Puf4 in filamentous fungi than with Puf3 in budding yeast. 3) The coregulated Puf4 target set in filamentous fungi expanded to include mitochondrial genes involved in the tricarboxylic acid (TCA) cycle and other nuclear-encoded RNAs with mitochondrial function not bound by Puf3 in budding yeast, observations that provide additional evidence for substantial rewiring of post-transcriptional regulation. 4) Puf3 also expanded and diversified its targets in filamentous fungi, gaining interactions with the mRNAs encoding the mitochondrial electron transport chain (ETC) complex I as well as hundreds of other mRNAs with nonmitochondrial functions. The many concerted and conserved changes in the RNA targets of Puf proteins strongly support an extensive role of RNA binding proteins in coordinating gene expression, as originally proposed by Keene. Rewiring of Puf-coordinated mRNA targets and transcriptional control of the same genes occurred at different points in evolution, suggesting that there have been distinct adaptations via RNA binding proteins and transcription factors. The changes in Puf targets and in the Puf proteins indicate an integral involvement of RNA binding proteins and their RNA targets in the adaptation, reprogramming, and function of gene expression.
机译:通过获取和丢失被特定调控RNA结合蛋白识别的序列来重新编程基因的表达模式,可能是生物调控程序发展的主要机制。我们发现,Puf3直系同源物的RNA靶标在五个真核世系中已经保守了100-500百万年。着眼于Puf蛋白及其80种真菌的靶标,我们为它们的进化历史构建了一个简约模型。该模型需要Puf靶标发生广泛而协调的变化,以及Puf基因数目的变化和RNA结合特异性的改变,包括:1)Puf3与200多个RNA结合,其蛋白质产物主要参与生产和代谢。线粒体复合物的组织早于发芽酵母和丝状真菌的起源,并且在整个发芽酵母的进化过程中一直维持了5亿年。 2)在丝状真菌中,值得注意的是,Puf4获得了超过150个祖先的Puf3靶标,其中一个谱系同时维持Puf3和Puf4作为调节剂,而一个姐妹谱系失去了Puf3作为这些RNA的调节剂。丝状真菌(N. crassa)中Puf4缺失后,这些mRNA的基因表达下降与发芽酵母(S. cerevisiae)中Puf3缺失时的表达上升相反,这表明RNA调控网络的输出与Puf4在酵母中不同。丝状真菌比带有Puf3的酵母更容易发芽。 3)在丝状真菌中定型的Puf4靶标扩展到包括三羧酸(TCA)周期中涉及的线粒体基因和其他不受Puf3约束的具有线粒体功能的核编码RNA,这些观察结果为进一步重布线提供了证据转录后调控。 4)Puf3还在丝状真菌中扩展和多样化了其靶标,与编码线粒体电子运输链(ETC)复合体I的mRNA以及数百种具有非线粒体功能的其他mRNA相互作用。 Puef蛋白的RNA靶标中许多协调一致的变化强烈支持了RNA结合蛋白在协调基因表达中的广泛作用,正如Keene最初提出的那样。 Puf协调的mRNA靶标的重新连接和同一基因的转录控制发生在进化的不同点,这表明通过RNA结合蛋白和转录因子有不同的适应性。 Puf靶标和Puf蛋白质的变化表明RNA结合蛋白及其RNA靶标在基因表达的适应,重编程和功能中不可或缺。

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