Homo sapiens
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA309759 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR3124500_1.fastq.gz | Fastqsanger.gz | |||
| SRR3124500_2.fastq.gz | Fastqsanger.gz | |||
| SRR3124501_1.fastq.gz | Fastqsanger.gz | |||
| SRR3124501_2.fastq.gz | Fastqsanger.gz | |||
| SRR3124502_1.fastq.gz | Fastqsanger.gz |
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Project description:The cGAS-STING pathway, a central component of the innate immune system, senses cytosolic DNA and induces interferon-stimulated genes (ISGs) to mediate inflammation. Here we report the unexpected discovery that cGAS senses dysfunctional protein production. Purified ribosomes interact with and stimulate the catalytic activity of recombinant cGAS in vitro. Disruption of the ribosome-associated protein quality control pathway, which detects and resolves ribosome collisions, results in cGAS- and STING-dependent ISG expression, and causes the re-localization of cGAS from the nucleus to the cytosol. Indeed, cGAS preferentially binds collided ribosomes in vitro, and other orthogonal perturbations that lead to elevated levels of collided ribosomes cause re-localization of cGAS as well. Thus, the cGAS-STING pathway senses and responds to translation stress. These findings have implications for the inflammatory responses to viral infection and tumorigenesis, both of which substantially reprogram cellular protein synthesis.
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