Institute of Healthy Ageing and Department of Genetics, Evolution & Environment, University College London, London WC1E 6BT, UK.
School of Health, Sport and Bioscience, University of East London, Stratford Campus, London E14 4LZ, UK.
Cell Rep. 2020 Mar 10;30(10):3240-3249.e4. doi: 10.1016/j.celrep.2020.02.058.
Target of Rapamycin Complex 1 (TORC1) signaling promotes growth and aging. Inhibition of TORC1 leads to reduced protein translation, which promotes longevity. TORC1-dependent post-transcriptional regulation of protein translation has been well studied, while analogous transcriptional regulation is less understood. Here we screen fission yeast mutants for resistance to Torin1, which inhibits TORC1 and cell growth. Cells lacking the GATA factor Gaf1 (gaf1Δ) grow normally even in high doses of Torin1. The gaf1Δ mutation shortens the chronological lifespan of non-dividing cells and diminishes Torin1-mediated longevity. Expression profiling and genome-wide binding experiments show that upon TORC1 inhibition, Gaf1 directly upregulates genes for small-molecule metabolic pathways and indirectly represses genes for protein translation. Surprisingly, Gaf1 binds to and downregulates the tRNA genes, so it also functions as a transcription factor for RNA polymerase III. Thus, Gaf1 controls the transcription of both protein-coding and tRNA genes to inhibit translation and growth downstream of TORC1.
雷帕霉素复合物 1(TORC1)信号促进生长和衰老。抑制 TORC1 会导致蛋白质翻译减少,从而促进长寿。TORC1 依赖的蛋白质翻译的转录后调控已经得到了很好的研究,而类似的转录调控则知之甚少。在这里,我们筛选了对抑制 TORC1 和细胞生长的 Torin1 具有抗性的裂殖酵母突变体。缺乏 GATA 因子 Gaf1(gaf1Δ)的细胞即使在高剂量的 Torin1 下也能正常生长。gaf1Δ突变缩短了非分裂细胞的时序寿命,并减弱了 Torin1 介导的长寿。表达谱和全基因组结合实验表明,在 TORC1 抑制后,Gaf1 直接上调小分子代谢途径的基因,并间接抑制蛋白质翻译的基因。令人惊讶的是,Gaf1 结合并下调 tRNA 基因,因此它也作为 RNA 聚合酶 III 的转录因子发挥作用。因此,Gaf1 控制蛋白质编码和 tRNA 基因的转录,以抑制 TORC1 下游的翻译和生长。