Peking University-Tsinghua University-National Institute of Biological Joint Graduate Program, School of Life Sciences, Peking University, Beijing, China.
National Institute of Biological Science, Beijing, China.
Elife. 2018 Aug 13;7:e36588. doi: 10.7554/eLife.36588.
Ribosome degradation through the autophagy-lysosome pathway is crucial for cell survival during nutrient starvation, but whether it occurs under normal growth conditions and contributes to animal physiology remains unaddressed. In this study, we identified RNST-2, a T2 family endoribonuclease, as the key enzyme that degrades ribosomal RNA in lysosomes. We found that loss of causes accumulation of rRNA and ribosomal proteins in enlarged lysosomes and both phenotypes are suppressed by blocking autophagy, which indicates that RNST-2 mediates autophagic degradation of ribosomal RNA in lysosomes. mutants are defective in embryonic and larval development and are short-lived. Remarkably, simultaneous loss of RNST-2 and de novo synthesis of pyrimidine nucleotides leads to complete embryonic lethality, which is suppressed by supplements of uridine or cytidine. Our study reveals an essential role of autophagy-dependent degradation of ribosomal RNA in maintaining nucleotide homeostasis during animal development.
通过自噬溶酶体途径降解核糖体对于营养饥饿期间的细胞存活至关重要,但它是否在正常生长条件下发生以及是否有助于动物生理学尚不清楚。在这项研究中,我们鉴定了 RNST-2,一种 T2 家族内切核酸酶,作为在溶酶体中降解核糖体 RNA 的关键酶。我们发现缺失导致 rRNA 和核糖体蛋白在增大的溶酶体中积累,并且这两种表型都被阻断自噬所抑制,这表明 RNST-2 介导溶酶体中核糖体 RNA 的自噬降解。突变体在胚胎和幼虫发育过程中存在缺陷并且寿命较短。值得注意的是,同时缺失 RNST-2 和嘧啶核苷酸的从头合成会导致完全的胚胎致死,而尿嘧啶或胞嘧啶的补充可以抑制这种致死。我们的研究揭示了核糖体 RNA 的自噬依赖性降解在动物发育过程中维持核苷酸稳态中的重要作用。