The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor.

Mutations in the basal transcription initiation/DNA repair factor TFIIH are responsible for three human disorders: xeroderma pigmentosum (XP), cockayne syndrome (CS) and trichothiodystrophy (TTD). The non-repair features of CS and TTD are thought to be due to a partial inactivation of the transcript...

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Hauptverfasser: Weeda, G, Rossignol, M, Fraser, R A, Winkler, G S, Vermeulen, W, van 't Veer, L J, Ma, L, Hoeijmakers, J H, Egly, J M
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1997
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC146752/
https://ncbi.nlm.nih.gov/pubmed/9173976
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