Abstract
Cells carefully modulate the rate of rRNA transcription in order to prevent an overinvestment in ribosome synthesis under less favorable nutritional conditions. In mammals, growth-dependent regulation of RNA polymerase I (Pol I) transcription is mediated by TIF-IA, an essential initiation factor that is active in extracts from growing but not starved or cycloheximide-treated mammalian cells. Here we report the molecular cloning and functional characterization of recombinant TIF-IA, which turns out to be the mammalian homolog of the yeast factor Rrn3p. We demonstrate that TIF-IA interacts with Pol I in the absence of template DNA, augments Pol I transcription in vivo and rescues transcription in extracts from growth-arrested cells in vitro.
MeSH Terms
3T3 Cells
Amino Acid Sequence
Animals
Blotting, Western
Cloning, Molecular
Genes, Reporter/genetics
HeLa Cells
Humans
Mice
Microscopy, Fluorescence
Molecular Sequence Data
Plasmids/genetics,metabolism
Pol1 Transcription Initiation Complex Proteins
RNA, Ribosomal/biosynthesis,metabolism
Saccharomyces cerevisiae/genetics
Saccharomyces cerevisiae Proteins
Sequence Alignment
Transcription Factors/chemistry,genetics,metabolism
Transfection
Yeasts/genetics
Chemicals
Pol1 Transcription Initiation Complex Proteins
RNA, Ribosomal
RRN3 protein, S cerevisiae
RRN3 protein, human
Rrn3 protein, mouse
Saccharomyces cerevisiae Proteins
Transcription Factors
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Bodem J
Division of Molecular Biology of the Cell II, German Cancer Research Center, Heidelberg.
Dobreva G
Hoffmann-Rohrer U
Iben S
Zentgraf H
Delius H
Vingron M
Grummt I
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