Literature DB >> 11265758

TIF-IA, the factor mediating growth-dependent control of ribosomal RNA synthesis, is the mammalian homolog of yeast Rrn3p.

J Bodem1, G Dobreva, U Hoffmann-Rohrer, S Iben, H Zentgraf, H Delius, M Vingron, I Grummt.   

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.

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Year:  2000        PMID: 11265758      PMCID: PMC1084264          DOI: 10.1093/embo-reports/kvd032

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  13 in total

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Authors:  D Buttgereit; G Pflugfelder; I Grummt
Journal:  Nucleic Acids Res       Date:  1985-11-25       Impact factor: 16.971

6.  RRN3 gene of Saccharomyces cerevisiae encodes an essential RNA polymerase I transcription factor which interacts with the polymerase independently of DNA template.

Authors:  R T Yamamoto; Y Nogi; J A Dodd; M Nomura
Journal:  EMBO J       Date:  1996-08-01       Impact factor: 11.598

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Authors:  B Moorefield; E A Greene; R H Reeder
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

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Journal:  Mol Cell Biol       Date:  1994-07       Impact factor: 4.272

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Authors:  A Schnapp; C Pfleiderer; H Rosenbauer; I Grummt
Journal:  EMBO J       Date:  1990-09       Impact factor: 11.598

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  64 in total

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7.  UBF activates RNA polymerase I transcription by stimulating promoter escape.

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