TUG C-terminal product nuclear localization and PPARγ binding

Exploratory Score: 0.850 Price: $0.50 Metabolic regulation Cell culture and mouse tissue Status: proposed

What This Experiment Tests

Exploratory experiment designed to discover new patterns targeting Tug (Aspscr1) in Cell culture and mouse tissue. Primary outcome: Nuclear localization and protein-protein interactions

Description

Investigation of the mechanism by which the TUG C-terminal cleavage product enters the nucleus and interacts with PPARγ and PGC-1α. This study demonstrated that after insulin-stimulated cleavage and GLUT4 release, the TUG C-terminal fragment translocates to the nucleus where it binds to transcriptional regulators to control gene expression programs involved in lipid oxidation and thermogenesis.

TARGET GENE
Tug (Aspscr1)
MODEL SYSTEM
Cell culture and mouse tissue
ESTIMATED COST
$0
TIMELINE
0 months
PATHWAY
PPARγ/PGC-1α transcriptional regulation
SOURCE
extracted_from_pmid_33686286
PRIMARY OUTCOME
Nuclear localization and protein-protein interactions

Scoring Dimensions

Info Gain 0.00 (25%) Feasibility 0.00 (20%) Hyp Coverage 0.00 (20%) Cost Effect. 0.00 (15%) Novelty 0.00 (10%) Ethical Safety 0.00 (10%) 0.850 composite

📖 Wiki Pages

PGC-1α (PPARGC1A) Targeted Therapies in NeurodegentherapeuticPGC-1α Activator Therapy for NeurodegenerationtreatmentPGC-1β ProteinproteinPGC-1 AlphaproteinPGC-1α (PPARGC1A)proteinPGC-1α ProteinredirectPGC-1α ProteinproteinPGC-1α and Mitochondrial Biogenesis Therapies for therapeuticPGC-1α Mitochondrial Biogenesis Comparison — AD/PDmechanism

Protocol

Subcellular fractionation, immunofluorescence microscopy, co-immunoprecipitation, chromatin immunoprecipitation

Expected Outcomes

TUG C-terminal product localizes to nucleus and binds PPARγ/PGC-1α

Success Criteria

Demonstration of nuclear localization and specific protein interactions

Related Hypotheses (0)

No related hypotheses

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