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smg-1

C. elegans

Serine/threonine-protein kinase smg-1

What the model saw

Gene: smg-1
Organism: Caenorhabditis elegans
Known functions: Serine/threonine-protein kinase smg-1. protein serine kinase activity. protein serine/threonine kinase activity.
View unredacted entry
Serine/threonine-protein kinase smg-1. protein serine kinase activity. protein serine/threonine kinase activity.

Solver output

Predicted influence
Pro-longevity
Confidence
65%
Mechanism
Genomic instability
Reasoning

SMG-1 is a PI3K-related serine/threonine protein kinase that is a core component of the nonsense-mediated mRNA decay (NMD) pathway, phosphorylating UPF1/SMG-2 to initiate degradation of aberrant transcripts containing premature stop codons. By eliminating faulty mRNAs, SMG-1 maintains transcriptome fidelity and proteostasis, reducing the accumulation of truncated or aberrant proteins that could be toxic. In C. elegans, NMD pathway components including smg-1 have been shown to influence lifespan, with loss of NMD function generally reducing longevity. Additionally, SMG-1 is an ATM/ATR-related kinase involved in DNA damage response signaling, contributing to genomic stability. These combined roles in RNA surveillance and genome integrity maintenance are consistent with a pro-longevity function.

Key pathways
nonsense-mediated mRNA decay (NMD)DNA damage response / ATM-ATR signalingRNA quality control / proteostasis
Longevity influence
Anti-longevity
Lifespan effect
Increase

GenAge curators classify each gene's normal function as promoting (Pro-Longevity) or opposing (Anti-Longevity) longevity, based on synthesis across studies. Loss-of-function effects can vary from this depending on the manipulation.

Advisor judgment

Answer
Incorrect
Mechanism
Incorrect
Reasoning quality
2/5
Failure mode
Confident wrong
Notes

The model predicted pro_longevity but the ground truth is anti_longevity. The model's reasoning about SMG-1's role in NMD and DNA damage response is partially correct mechanistically, but it drew the wrong conclusion about the direction of longevity influence. In C. elegans, smg-1 loss-of-function actually extends lifespan, making it anti-longevity (i.e., the gene normally suppresses longevity). The model incorrectly assumed that because NMD maintains transcriptome fidelity, loss of NMD would reduce longevity - but the actual experimental data shows the opposite. The model's reasoning that 'loss of NMD function generally reducing longevity' is factually incorrect for smg-1 in C. elegans. The model had moderate confidence (0.65) but was wrong on both the answer and the mechanistic interpretation of the experimental outcome.

Raw API responses

solver

{
  "reasoning": "SMG-1 is a PI3K-related serine/threonine protein kinase that is a core component of the nonsense-mediated mRNA decay (NMD) pathway, phosphorylating UPF1/SMG-2 to initiate degradation of aberrant transcripts containing premature stop codons. By eliminating faulty mRNAs, SMG-1 maintains transcriptome fidelity and proteostasis, reducing the accumulation of truncated or aberrant proteins that could be toxic. In C. elegans, NMD pathway components including smg-1 have been shown to influence lifespan, with loss of NMD function generally reducing longevity. Additionally, SMG-1 is an ATM/ATR-related kinase involved in DNA damage response signaling, contributing to genomic stability. These combined roles in RNA surveillance and genome integrity maintenance are consistent with a pro-longevity function.",
  "confidence": 0.65,
  "key_pathways": [
    "nonsense-mediated mRNA decay (NMD)",
    "DNA damage response / ATM-ATR signaling",
    "RNA quality control / proteostasis"
  ],
  "mechanism_class": "genomic_instability",
  "longevity_influence": "pro_longevity"
}

advisor

{
  "notes": "The model predicted pro_longevity but the ground truth is anti_longevity. The model's reasoning about SMG-1's role in NMD and DNA damage response is partially correct mechanistically, but it drew the wrong conclusion about the direction of longevity influence. In C. elegans, smg-1 loss-of-function actually extends lifespan, making it anti-longevity (i.e., the gene normally suppresses longevity). The model incorrectly assumed that because NMD maintains transcriptome fidelity, loss of NMD would reduce longevity - but the actual experimental data shows the opposite. The model's reasoning that 'loss of NMD function generally reducing longevity' is factually incorrect for smg-1 in C. elegans. The model had moderate confidence (0.65) but was wrong on both the answer and the mechanistic interpretation of the experimental outcome.",
  "failure_mode": "confident_wrong",
  "answer_correct": false,
  "mechanism_correct": false,
  "reasoning_quality": 2,
  "ground_truth_questionable": false
}
smg-1 · Caenorhabditis elegans | Aging biology eval