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Differential remodelling of peroxisome function underpins the environmental and metabolic adaptability of diplonemids and kinetoplastids

机译:过氧化物酶体功能的差异重塑增强了二烯酮和动质体的环境和代谢适应性

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摘要

The remodelling of organelle function is increasingly appreciated as a central driver of eukaryotic biodiversity and evolution. Kinetoplastids including Trypanosoma and Leishmania have evolved specialised peroxisomes, called glycosomes. Glycosomes uniquely contain a glycolytic pathway as well as other enzymes, which underpin the physiological flexibility of these major humanpathogens. The sister group of kinetoplastids are the diplonemids, which are among the most abundant eukaryotes in marine plankton. Here we demonstrate the compartmentalisation of gluconeogenesis, or glycolysis in reverse, in the peroxisomes of the free-living marine diplonemid, Diplonema papillatum. Our results suggest that peroxisome modification was already underway in the common ancestor of kinetoplastids and diplonemids, and raise the possibility that the central importance of gluconeogenesis to carbon metabolism in theheterotrophic free-living ancestor may have been an important selective driver. Our data indicate that peroxisome modification is not confined to the kinetoplastid lineage, but has also been a factor in the success of their free-living euglenozoan relatives.
机译:细胞器功能的重塑日益成为真核生物多样性和进化的主要驱动力。包括锥虫和利什曼原虫在内的动素体已经进化出专门的过氧化物酶体,称为糖体。糖体独特地包含糖酵解途径以及其他酶,这些酶支撑了这些主要人类病原体的生理柔韧性。动质体的姊妹组是二倍体,这是海洋浮游生物中最丰富的真核生物之一。在这里,我们证明了在自由生活的海洋二烯酮,Diplonema papillatum的过氧化物酶体中糖异生或反糖酵解的区室化。我们的结果表明,过氧化物酶体修饰已经在动素体和二倍体酰胺的共同祖先中进行,并提出了异养自由祖先中糖异生对碳代谢的重要作用可能是重要的选择性驱动因素。我们的数据表明,过氧化物酶体修饰不仅限于运动质体谱系,而且还成为其自由生活的裸藻动物亲属成功的因素。

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