Vernekar Dipti Vinayak, Bhargava Purnima
Centre for Cellular and Molecular Biology (Council of Scientific and Industrial Research), Uppal Road, Hyderabad 500007, India.
Centre for Cellular and Molecular Biology (Council of Scientific and Industrial Research), Uppal Road, Hyderabad 500007, India.
Biochim Biophys Acta. 2015 Nov;1849(11):1340-53. doi: 10.1016/j.bbagrm.2015.09.010. Epub 2015 Sep 28.
Yeast Bud27, an unconventional prefoldin is reported to affect the expression of nutrient-responsive genes, translation initiation and assembly of the multi-subunit eukaryotic RNA polymerases (pols), at a late step. We found that Bud27 associates with pol III in active as well as repressed states. Pol III transcription and occupancy at the target genes reduce with the deletion of BUD27. It promotes the interaction of pol III with the chromatin remodeler RSC found on most of the pol III targets, and with the heat shock protein Ssa4, which helps in nuclear import of the assembled pol III. Under nutrient-starvation, Ssa4-pol III interaction increases, while pol III remains inside the nucleus. Bud27 but not Ssa4 is required for RSC-pol III interaction, which reduces under nutrient-starvation. In the bud27Δ cells, total protein level of the largest pol III subunit Rpc160 but not of Rpc128, Rpc34 and Rpc53 subunits is reduced. This is accompanied by lower transcription of RPC128 gene and lower RPC160 translation due to reduced association of mRNA with the ribosomes. The resultant alteration in the normal cellular ratio of the two largest subunits of pol III core leads to reduced association of other pol III subunits and hampers the normal assembly of pol III at an early step in the cytoplasm. Our results show that Bud27 is required in multiple activities responsible for pol III biogenesis and activity.
据报道,酵母Bud27是一种非常规的前折叠素,在后期会影响营养响应基因的表达、翻译起始以及多亚基真核RNA聚合酶(pols)的组装。我们发现Bud27在活性状态和抑制状态下均与聚合酶III相关联。随着BUD27的缺失,聚合酶III在靶基因处的转录和占据率降低。它促进了聚合酶III与在大多数聚合酶III靶标上发现的染色质重塑因子RSC以及热休克蛋白Ssa4的相互作用,Ssa4有助于组装好的聚合酶III的核输入。在营养饥饿条件下,Ssa4 - 聚合酶III的相互作用增强,而聚合酶III仍留在细胞核内。RSC - 聚合酶III的相互作用需要Bud27而非Ssa4,这种相互作用在营养饥饿时会减弱。在bud27Δ细胞中,最大的聚合酶III亚基Rpc160的总蛋白水平降低,而Rpc128、Rpc34和Rpc53亚基的总蛋白水平未降低。这伴随着RPC128基因转录降低以及由于mRNA与核糖体的结合减少导致的Rpc160翻译降低。聚合酶III核心的两个最大亚基的正常细胞比例的这种改变导致其他聚合酶III亚基的结合减少,并在细胞质的早期阶段阻碍了聚合酶III的正常组装。我们的结果表明,Bud27在负责聚合酶III生物合成和活性的多种活动中是必需的。