IMG2
S. cerevisiae
mitochondrial 54S ribosomal protein mL49 IMG2
What the model saw
Gene: IMG2 Organism: Saccharomyces cerevisiae Known functions: mitochondrial 54S ribosomal protein mL49 IMG2. structural constituent of ribosome.
View unredacted entry
mitochondrial 54S ribosomal protein mL49 IMG2. structural constituent of ribosome.
Solver output
IMG2 encodes the mitochondrial large ribosomal subunit protein mL49 (54S subunit), which serves as a structural constituent of the mitochondrial ribosome. Proper assembly and function of the mitochondrial ribosome is essential for translation of the 8 mitochondrially-encoded subunits of the oxidative phosphorylation complexes in yeast. Loss of mitochondrial ribosomal integrity leads to impaired OXPHOS, reduced mitochondrial membrane potential, and increased reactive oxygen species — all hallmarks of mitochondrial dysfunction associated with aging. In yeast, maintenance of mitochondrial function and mitochondrial genome integrity (petite-negative phenotype) is linked to replicative and chronological lifespan. Therefore, the normal function of IMG2 in supporting mitochondrial translation supports mitochondrial health and is expected to be pro-longevity.
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
The model predicted pro_longevity but the ground truth is anti_longevity. The model's reasoning follows a plausible but incorrect logic: it assumes that because IMG2 supports mitochondrial ribosome function and OXPHOS, it must be pro-longevity. However, in yeast, deletion of mitochondrial ribosomal proteins like IMG2 can actually extend lifespan, consistent with the concept that reduced mitochondrial translation/OXPHOS can be beneficial for longevity (similar to how mitochondrial ribosome mutations extend lifespan in C. elegans). The model failed to consider that anti_longevity classification means deletion of IMG2 extends lifespan, which fits with the broader finding that reduced mitochondrial function can promote longevity. The model's confidence of 0.62 is moderate but still wrong. The mechanistic reasoning is also incorrect in its directionality — it assumes loss of function = bad for lifespan, when the opposite is true here.
Raw API responses
solver
{
"reasoning": "IMG2 encodes the mitochondrial large ribosomal subunit protein mL49 (54S subunit), which serves as a structural constituent of the mitochondrial ribosome. Proper assembly and function of the mitochondrial ribosome is essential for translation of the 8 mitochondrially-encoded subunits of the oxidative phosphorylation complexes in yeast. Loss of mitochondrial ribosomal integrity leads to impaired OXPHOS, reduced mitochondrial membrane potential, and increased reactive oxygen species — all hallmarks of mitochondrial dysfunction associated with aging. In yeast, maintenance of mitochondrial function and mitochondrial genome integrity (petite-negative phenotype) is linked to replicative and chronological lifespan. Therefore, the normal function of IMG2 in supporting mitochondrial translation supports mitochondrial health and is expected to be pro-longevity.",
"confidence": 0.62,
"key_pathways": [
"mitochondrial translation",
"oxidative phosphorylation",
"mitochondrial ribosome assembly"
],
"mechanism_class": "mitochondrial_dysfunction",
"longevity_influence": "pro_longevity"
}advisor
{
"notes": "The model predicted pro_longevity but the ground truth is anti_longevity. The model's reasoning follows a plausible but incorrect logic: it assumes that because IMG2 supports mitochondrial ribosome function and OXPHOS, it must be pro-longevity. However, in yeast, deletion of mitochondrial ribosomal proteins like IMG2 can actually extend lifespan, consistent with the concept that reduced mitochondrial translation/OXPHOS can be beneficial for longevity (similar to how mitochondrial ribosome mutations extend lifespan in C. elegans). The model failed to consider that anti_longevity classification means deletion of IMG2 extends lifespan, which fits with the broader finding that reduced mitochondrial function can promote longevity. The model's confidence of 0.62 is moderate but still wrong. The mechanistic reasoning is also incorrect in its directionality — it assumes loss of function = bad for lifespan, when the opposite is true here.",
"failure_mode": "confident_wrong",
"answer_correct": false,
"mechanism_correct": false,
"reasoning_quality": 2,
"ground_truth_questionable": false
}