Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, SK, S7N 5B4, Canada.
Department of Biology and Genetics Institute, University of Florida, Gainesville, FL, 32611, USA.
BMC Biol. 2019 Jul 16;17(1):56. doi: 10.1186/s12915-019-0675-z.
Adaptive responses to stress are essential for cell and organismal survival. In metazoans, little is known about the impact of environmental stress on RNA homeostasis.
By studying the regulation of a cadmium-induced gene named numr-1 in Caenorhabditis elegans, we discovered that disruption of RNA processing acts as a signal for environmental stress. We find that NUMR-1 contains motifs common to RNA splicing factors and influences RNA splicing in vivo. A genome-wide screen reveals that numr-1 is strongly and specifically induced by silencing of genes that function in basal RNA metabolism including subunits of the metazoan integrator complex. Human integrator processes snRNAs for functioning with splicing factors, and we find that silencing of C. elegans integrator subunits disrupts snRNA processing, causes aberrant pre-mRNA splicing, and induces the heat shock response. Cadmium, which also strongly induces numr-1, has similar effects on RNA and the heat shock response. Lastly, we find that heat shock factor-1 is required for full numr-1 induction by cadmium.
Our results are consistent with a model in which disruption of integrator processing of RNA acts as a molecular damage signal initiating an adaptive stress response mediated by heat shock factor-1. When numr-1 is induced via this pathway in C. elegans, its function in RNA metabolism may allow it to mitigate further damage and thereby promote tolerance to cadmium.
适应应激反应对于细胞和生物机体的生存至关重要。在多细胞生物中,人们对环境应激对 RNA 稳态的影响知之甚少。
通过研究秀丽隐杆线虫中一种名为 numr-1 的镉诱导基因的调控,我们发现 RNA 加工的破坏可作为环境应激的信号。我们发现 NUMR-1 含有 RNA 剪接因子常见的基序,并影响体内的 RNA 剪接。全基因组筛选表明,numr-1 强烈且特异性地被参与基础 RNA 代谢的基因失活所诱导,包括真核生物整合体复合物的亚基。人类整合体处理 snRNA 以与剪接因子一起发挥作用,我们发现线虫整合体亚基的沉默会破坏 snRNA 加工,导致异常的前体 mRNA 剪接,并诱导热休克反应。镉也强烈诱导 numr-1 的表达,对 RNA 和热休克反应也有类似的影响。最后,我们发现热休克因子-1 是镉完全诱导 numr-1 所必需的。
我们的结果与以下模型一致,即整合体对 RNA 的加工破坏作为一种分子损伤信号,启动由热休克因子-1 介导的适应性应激反应。当 numr-1 通过这条途径在秀丽隐杆线虫中被诱导时,它在 RNA 代谢中的功能可能使其能够减轻进一步的损伤,从而促进对镉的耐受性。