Université de Paris, Unité de Biologie Fonctionnelle et Adaptative (BFA), UMR 8251, CNRS, 4 rue Marie-Andrée Lagroua Weill-Hallé, F-75013 Paris, France.
Department of Life Sciences, Imperial College London, London SW7 2AZ, England, UK.
J Cell Sci. 2019 Sep 2;132(17):jcs228601. doi: 10.1242/jcs.228601.
In humans, ribosome biogenesis mainly occurs in nucleoli following two alternative pre-rRNA processing pathways differing in the order in which cleavages take place but not by the sites of cleavage. To uncover the role of the nucleolar NAD-dependent deacetylase sirtuin 7 in the synthesis of ribosomal subunits, pre-rRNA processing was analyzed after sirtinol-mediated inhibition of sirtuin 7 activity or depletion of sirtuin 7 protein. We thus reveal that sirtuin 7 activity is a critical regulator of processing of 45S, 32S and 30S pre-rRNAs. Sirtuin 7 protein is primarily essential to 45S pre-rRNA cleavage at site 2, which is the first step of processing pathway 2. Furthermore, we demonstrate that sirtuin 7 physically interacts with Nop56 and the GAR domain of fibrillarin, and propose that this could interfere with fibrillarin-dependent cleavage. Sirtuin 7 depletion results in the accumulation of 5' extended forms of 32S pre-rRNA, and also influences the localization of fibrillarin. Thus, we establish a close relationship between sirtuin 7 and fibrillarin, which might determine the processing pathway used for ribosome biogenesis.
在人类中,核糖体生物发生主要发生在核仁中,遵循两种替代的前 rRNA 加工途径,这些途径的区别在于切割的顺序,而不是切割的位置。为了揭示核仁 NAD 依赖性去乙酰化酶 Sirtuin 7 在核糖体亚基合成中的作用,在 Sirtinol 介导的 Sirtuin 7 活性抑制或 Sirtuin 7 蛋白耗竭后分析了前 rRNA 加工。因此,我们揭示了 Sirtuin 7 活性是 45S、32S 和 30S 前 rRNA 加工的关键调节剂。Sirtuin 7 蛋白主要对 45S 前 rRNA 在位点 2 的切割至关重要,这是加工途径 2 的第一步。此外,我们证明 Sirtuin 7 与 Nop56 和纤维蛋白的 GAR 结构域物理相互作用,并提出这可能干扰纤维蛋白依赖性切割。Sirtuin 7 的耗竭导致 32S 前 rRNA 的 5'延伸形式的积累,并且还影响纤维蛋白的定位。因此,我们建立了 Sirtuin 7 和纤维蛋白之间的密切关系,这可能决定了核糖体生物发生中使用的加工途径。