Target intelligence / Profile preview

Mediator complex subunit 15 (MED15)

Target
MED15
Molecular classification
Transcription factor coactivator, Mediator complex subunit, Prion-like protein (domain-level), Other (multimeric protein complex member)
01

Overview

Mediator complex subunit 15 (MED15) is a general transcriptional coactivator and a member of the tail module within the multi-subunit Mediator complex[4][2]. It acts as a crucial bridge between transcriptional activators and the RNA polymerase II enzyme, conveying regulatory signals to enable or modulate gene expression[4][3]. MED15 contains prion-like domains with polyglutamine tracts, which give it the ability to undergo conformational changes, form protein aggregates, and possibly contribute to epigenetic regulation[2][3]. Its protein interaction domains (including multiple activator-binding domains and KIX domain) serve as binding sites for a wide array of transcription factors[3][4]. MED15 is conserved across eukaryotes, essential for normal cellular activities, and implicated in cell differentiation, stress response, and immunity, especially in model plants and yeasts[1][5]. In humans, MED15 is associated with regulatory events in lipid metabolism, cellular stress adaptation, and developmental signaling pathways[4][5]. Disturbances in its gene or protein aggregation behavior have potential implications in cancer, neurodegeneration, and genetic syndromes, but no drugs currently target MED15 directly.

Other names
PCQAPARC105CTG7ATIG-1TNRC7Gal11 (yeast)Spt13 (yeast)Positive cofactor 2 glutamine/Q-rich-associated proteinActivator-recruited cofactor 105 kDa componentTPA-inducible gene 1 proteinTrinucleotide repeat-containing gene 7 protein
02

Biological functions

Bridging enhancers and promoters for gene transcriptionRecruitment of RNA polymerase IISignal integration from transcriptional activatorsModulation of gene expression in response to cellular signals (e.g., stress, hormone signaling)Protein–protein interaction hub for transcription factors
03

Disease associations

Cancer (implicated due to transcriptional dysregulation; direct disease relevance for MED15 is suggested, but specific mechanisms are still under research)Neurodegenerative disease (prion-like and aggregation properties)Genetic syndromes (gene located at deleted region in DiGeorge syndrome)Other (possible roles in inflammatory and metabolic diseases via transcriptional regulation)
04

Safety considerations

Protein aggregation and amyloid-like transitions could theoretically pose challenges if targeted, such as off-target effects on transcriptional regulation or cellular homeostasisMutation or dysregulation may affect multiple signaling pathways due to hub function

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