Abstract
An in vitro transcription system consisting of partially purified transcription initiation factor(s) and purified RNA polymerase I from Acanthamoeba castellanii was used to study the mechanism of faithful initiation of ribosomal RNA transcription. Formation of a preinitiation complex between one or several auxiliary transcription proteins and the DNA template in the absence of RNA polymerase I was demonstrated. A series of 3'- and 5'-deletion mutants of the template was used in prebinding competition experiments and provided evidence for three distinct functional regions of the promoter: core motif A interacts with the transcription initiation factor(s) and is required for faithful transcription; the start motif is required for transcription, but it can be deleted without affecting the binding of transcription initiation factor(s); and motif B stabilizes preinitiation complex formation (in addition to core motif A), but it is dispensable for faithful initiation of transcription.
MeSH Terms
Amoeba/genetics,metabolism
Animals
Binding, Competitive
Chromosome Deletion
DNA/metabolism
Operon
Proteins/metabolism
RNA, Ribosomal/metabolism
Transcription Factors/metabolism
Transcription, Genetic
Chemicals
Proteins
RNA, Ribosomal
Transcription Factors
DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Iida C T
Kownin P
Paule M R
References (13)
13 references, click to expand
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