CAS Key Laboratory of Innate Immunity and Chronic Disease, CAS Centre for Excellence in Molecular Cell Science, School of Life Sciences, University of Science and Technology of China and The First Affiliated Hospital of University of Science and Technology of China, Hefei, China.
Translational Research Institute, Henan Provincial People's Hospital, Academy of Medical Science, Zhengzhou University, Zhengzhou, China.
EMBO Rep. 2020 Apr 3;21(4):e48796. doi: 10.15252/embr.201948796. Epub 2020 Mar 9.
The long noncoding RNA GUARDIN functions to protect genome stability. Inhibiting GUARDIN expression can alter cell fate decisions toward senescence or apoptosis, but the underlying molecular signals are unknown. Here, we show that GUARDIN is an essential component of a transcriptional repressor complex involving LRP130 and PGC1α. GUARDIN acts as a scaffold to stabilize LRP130/PGC1α heterodimers and their occupancy at the FOXO4 promotor. Destabilizing this complex by silencing of GUARDIN, LRP130, or PGC1α leads to increased expression of FOXO4 and upregulation of its target gene p21, thereby driving cells into senescence. We also found that GUARDIN expression was induced by rapamycin, an agent that suppresses cell senescence. FOS-like antigen 2 (FOSL2) acts as a transcriptional repressor of GUARDIN, and lower FOSL2 levels in response to rapamycin correlate with increased levels of GUARDIN. Together, these results demonstrate that GUARDIN inhibits p21-dependent senescence through a LRP130-PGC1α-FOXO4 signaling axis, and moreover, GUARDIN contributes to the anti-aging activities of rapamycin.
长链非编码 RNA GUARDIN 具有保护基因组稳定性的功能。抑制 GUARDIN 的表达可以改变细胞命运决定走向衰老或凋亡,但潜在的分子信号尚不清楚。在这里,我们表明 GUARDIN 是涉及 LRP130 和 PGC1α 的转录抑制复合物的必需组成部分。GUARDIN 作为支架稳定 LRP130/PGC1α 异二聚体及其在 FOXO4 启动子上的占据。通过沉默 GUARDIN、LRP130 或 PGC1α 使该复合物失稳,导致 FOXO4 的表达增加,并上调其靶基因 p21,从而使细胞进入衰老。我们还发现,雷帕霉素(一种抑制细胞衰老的药物)诱导 GUARDIN 的表达。FOS 样抗原 2(FOSL2)是 GUARDIN 的转录抑制剂,雷帕霉素引起的 FOSL2 水平降低与 GUARDIN 水平的升高相关。总之,这些结果表明 GUARDIN 通过 LRP130-PGC1α-FOXO4 信号轴抑制 p21 依赖性衰老,此外,GUARDIN 有助于雷帕霉素的抗衰老作用。