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葡萄糖饥饿或热休克对酵母解旋酶Ded1的下调差异性地损害了Ded1依赖性mRNA的翻译。

Down-Regulation of Yeast Helicase Ded1 by Glucose Starvation or Heat-Shock Differentially Impairs Translation of Ded1-Dependent mRNAs.

作者信息

Sen Neelam Dabas, Zhang Hongen, Hinnebusch Alan G

机构信息

Division of Molecular and Cellular Biology, Eunice K. Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

School of Life Sciences, Jawaharlal Nehru University, New Delhi 110067, India.

出版信息

Microorganisms. 2021 Nov 23;9(12):2413. doi: 10.3390/microorganisms9122413.

Abstract

Ded1 is an essential DEAD-box helicase in yeast that broadly stimulates translation initiation and is critical for mRNAs with structured 5'UTRs. Recent evidence suggests that the condensation of Ded1 in mRNA granules down-regulates Ded1 function during heat-shock and glucose starvation. We examined this hypothesis by determining the overlap between mRNAs whose relative translational efficiencies (TEs), as determined by ribosomal profiling, were diminished in either stressed WT cells or in mutants examined in non-stress conditions. Only subsets of the Ded1-hyperdependent mRNAs identified in mutant cells exhibited strong TE reductions in glucose-starved or heat-shocked WT cells, and those down-regulated by glucose starvation also exhibited hyper-dependence on initiation factor eIF4B, and to a lesser extent eIF4A, for efficient translation in non-stressed cells. These findings are consistent with recent proposals that the dissociation of Ded1 from mRNA 5'UTRs and the condensation of Ded1 contribute to reduced Ded1 function during stress, and they further suggest that the down-regulation of eIF4B and eIF4A functions also contributes to the translational impairment of a select group of Ded1 mRNA targets with heightened dependence on all three factors during glucose starvation.

摘要

Ded1是酵母中一种必需的DEAD盒解旋酶,广泛刺激翻译起始,对于具有结构化5'UTR的mRNA至关重要。最近的证据表明,在热休克和葡萄糖饥饿期间,Ded1在mRNA颗粒中的凝聚会下调其功能。我们通过确定核糖体分析所测定的相对翻译效率(TE)在应激野生型细胞或非应激条件下检测的突变体中降低的mRNA之间的重叠来检验这一假设。在突变体细胞中鉴定出的Ded1超依赖性mRNA的子集中,只有一部分在葡萄糖饥饿或热休克的野生型细胞中表现出强烈的TE降低,并且那些在葡萄糖饥饿时下调的mRNA在非应激细胞中高效翻译时也表现出对起始因子eIF4B以及在较小程度上对eIF4A的超依赖性。这些发现与最近的观点一致,即Ded1从mRNA 5'UTR解离以及Ded1的凝聚导致应激期间Ded1功能降低,并且它们进一步表明,eIF4B和eIF4A功能的下调也导致了一组特定的Ded1 mRNA靶标的翻译受损,这些靶标在葡萄糖饥饿期间对所有这三种因子的依赖性增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39d/8706886/7261878c75df/microorganisms-09-02413-g001.jpg

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