Core Function: TAF10 is integral to the TFIID basal transcription factor complex, which binds promoters (with/without TATA boxes) to assemble the pre-initiation complex (PIC) .
Subunit Interactions: Forms stable interactions with TBP, TAF8, TAF9, and TAF13, enabling TFIID’s structural asymmetry and promoter selectivity .
SAGA/STAGA/PCAF: TAF10 is shared between TFIID and histone acetyltransferase complexes (e.g., SAGA), linking promoter recognition to chromatin remodeling .
Cytoplasmic Assembly: Participates in a cytoplasmic TAF2–TAF8–TAF10 subcomplex, which primes nuclear import and holo-TFIID assembly .
Embryogenesis: TAF10 knockout in mice causes embryonic lethality by E5.5 due to disrupted TFIID stability and cell cycle arrest .
Erythropoiesis: TAF10 ablation blocks erythroid differentiation, deregulating GATA1 and its targets (e.g., hemoglobin genes) .
Neurological Disorders: Mutations in TAF2 (a TAF10 interactor) correlate with neurodevelopmental defects .
Cancer: TAF10-dependent cyclin E regulation suggests roles in cell proliferation .
Antibodies: Polyclonal antibodies against recombinant TAF10 enable immunoprecipitation and localization studies .
Cellular Models: Conditional TAF10 knockout in F9 embryonal carcinoma cells reveals TFIID’s role in pluripotency .
Complex Stoichiometry: Mass spectrometry reveals dynamic TFIID/SAGA composition during erythroid differentiation .
Gene-Specific Recruitment: ChIP-seq data show TAF10 enrichment at the GATA1 locus in fetal erythroid cells .
The initiation of transcription by RNA polymerase II requires the coordinated activities of more than 70 polypeptides. TFIID, which includes TAF10, is essential for this process. TFIID binds to the core promoter region of genes to position RNA polymerase II correctly, serving as a scaffold for the assembly of the transcription complex and acting as a channel for regulatory signals .
TAF10, specifically, is involved in several critical functions:
TAF10 interacts with several other proteins and factors within the cell:
Studies have shown that TAF10 is required for transcriptional activation by the estrogen receptor, progression through the cell cycle, and certain cellular differentiation programs .