Abstract
Mouse RNA polymerase I requires at least two chromatographically distinct transcription factors (designated TIF-IA and TIF-IB) to initiate transcription accurately and efficiently in vitro. In this paper we describe the partial purification of TIF-IA by a four-step fractionation procedure. The amount or activity of TIF-IA fluctuates in response to the physiological state of the cells. Extracts from quiescent cells are incapable of specific transcription and do not contain detectable levels of TIF-IA. Transcriptionally inactive extracts can be restored by the addition of TIF-IA preparations that have been highly purified from exponentially growing cells. During the fractionating procedure TIF-IA co-purifies with RNA polymerase I, suggesting that it is functionally associated with the transcribing enzyme. We suggest that only those enzyme molecules that are associated with TIF-IA are capable to interact with TIF-IB and to initiate transcription.
MeSH Terms
Animals
Carcinoma, Ehrlich Tumor/analysis
Cell Division
Cell-Free System
Gene Expression Regulation
Mice
Neoplasm Proteins/isolation & purification,physiology
RNA Polymerase I/metabolism
RNA, Neoplasm/biosynthesis,genetics
RNA, Ribosomal/biosynthesis,genetics
Transcription Factors/physiology
Transcription, Genetic
Chemicals
Neoplasm Proteins
RNA, Neoplasm
RNA, Ribosomal
Transcription Factors
RNA Polymerase I
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Buttgereit D
Pflugfelder G
Grummt I
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