← Browse entries

rpl-10L

C. elegans

Large ribosomal subunit protein uL16

What the model saw

Gene: rpl-10L
Organism: Caenorhabditis elegans
Known functions: Large ribosomal subunit protein uL16. structural constituent of ribosome.
View unredacted entry
Large ribosomal subunit protein uL16. structural constituent of ribosome.

Solver output

Predicted influence
Anti-longevity
Confidence
72%
Mechanism
Deregulated nutrient sensing
Reasoning

rpl-10L encodes the large ribosomal subunit protein uL16, a core structural component of the 60S ribosomal subunit required for mRNA translation. Ribosomal protein levels are tightly coupled to TOR (Target of Rapamycin) signaling, the master nutrient-sensing pathway: high TOR activity upregulates ribosome biogenesis and global translation, which is associated with accelerated aging, while reduced ribosomal activity extends lifespan. In C. elegans, partial loss-of-function of multiple large ribosomal subunit proteins (e.g., rpl-5, rpl-11) has been shown to extend lifespan via reduced translation rates and activation of stress-response pathways. As a structural constituent of the ribosome, rpl-10L's normal function sustains high translational capacity, which promotes growth and reproduction at the cost of longevity. Reduction of ribosomal protein function also intersects with the IIS/DAF-16 and germline signaling pathways to modulate lifespan in worms.

Key pathways
TOR/ribosome biogenesis signalingglobal mRNA translation regulationIIS/DAF-16 longevity pathway
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
Correct
Mechanism
Correct
Reasoning quality
4/5
Failure mode
Correct
Notes

The model correctly predicted anti_longevity for rpl-10L. The mechanistic reasoning is sound: ribosomal proteins like rpl-10L support high translational capacity, and their reduction (loss-of-function) extends lifespan in C. elegans, making the normal function anti-longevity. The model correctly cites analogous ribosomal proteins (rpl-5, rpl-11) and correctly links ribosome function to TOR/nutrient sensing. The mechanism class "deregulated_nutrient_sensing" is a reasonable but slightly imprecise label — "translation/ribosome biogenesis" would be more direct, though TOR signaling is closely related. Overall, the reasoning is well-grounded and the answer is correct.

Raw API responses

solver

{
  "reasoning": "rpl-10L encodes the large ribosomal subunit protein uL16, a core structural component of the 60S ribosomal subunit required for mRNA translation. Ribosomal protein levels are tightly coupled to TOR (Target of Rapamycin) signaling, the master nutrient-sensing pathway: high TOR activity upregulates ribosome biogenesis and global translation, which is associated with accelerated aging, while reduced ribosomal activity extends lifespan. In C. elegans, partial loss-of-function of multiple large ribosomal subunit proteins (e.g., rpl-5, rpl-11) has been shown to extend lifespan via reduced translation rates and activation of stress-response pathways. As a structural constituent of the ribosome, rpl-10L's normal function sustains high translational capacity, which promotes growth and reproduction at the cost of longevity. Reduction of ribosomal protein function also intersects with the IIS/DAF-16 and germline signaling pathways to modulate lifespan in worms.",
  "confidence": 0.72,
  "key_pathways": [
    "TOR/ribosome biogenesis signaling",
    "global mRNA translation regulation",
    "IIS/DAF-16 longevity pathway"
  ],
  "mechanism_class": "deregulated_nutrient_sensing",
  "longevity_influence": "anti_longevity"
}

advisor

{
  "notes": "The model correctly predicted anti_longevity for rpl-10L. The mechanistic reasoning is sound: ribosomal proteins like rpl-10L support high translational capacity, and their reduction (loss-of-function) extends lifespan in C. elegans, making the normal function anti-longevity. The model correctly cites analogous ribosomal proteins (rpl-5, rpl-11) and correctly links ribosome function to TOR/nutrient sensing. The mechanism class \"deregulated_nutrient_sensing\" is a reasonable but slightly imprecise label — \"translation/ribosome biogenesis\" would be more direct, though TOR signaling is closely related. Overall, the reasoning is well-grounded and the answer is correct.",
  "failure_mode": "correct",
  "answer_correct": true,
  "mechanism_correct": true,
  "reasoning_quality": 4,
  "ground_truth_questionable": false
}