The FBP interacting repressor targets TFIIH to inhibit activated transcription.

Article Details

Citation

Liu J, He L, Collins I, Ge H, Libutti D, Li J, Egly JM, Levens D

The FBP interacting repressor targets TFIIH to inhibit activated transcription.

Mol Cell. 2000 Feb;5(2):331-41.

PubMed ID
10882074 [ View in PubMed
]
Abstract

FUSE-binding protein (FBP) binds the single-stranded far upstream element of active c-myc genes, possesses potent transcription activation and repression domains, and is necessary for c-myc expression. A novel 60 kDa protein, the FBP interacting repressor (FIR), blocked activator-dependent, but not basal, transcription through TFIIH. Recruited through FBP's nucleic acid-binding domain, FIR formed a ternary complex with FBP and FUSE. FIR repressed a c-myc reporter via the FUSE. The amino terminus of FIR contained an activator-selective repression domain capable of acting in cis or even in trans in vivo and in vitro. The repression domain of FIR targeted only TFIIH's p89/XPB helicase, required at several stages in transcription, but not factors required for promoter selection. Thus, FIR locks TFIIH in an activation-resistant configuration that still supports basal transcription.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Cyclin-dependent kinase 7P50613Details
Far upstream element-binding protein 1Q96AE4Details