Literature DB >> 8423793

The rRNA enhancer regulates rRNA transcription in Saccharomyces cerevisiae.

B E Morrow1, S P Johnson, J R Warner.   

Abstract

In Saccharomyces cerevisiae, the rRNA genes are organized as a tandem array of head-to-tail repeats. An enhancer of rRNA transcription is present just at the end of each transcription unit, 2 kb away from the next one. This enhancer is unusual for S. cerevisiae in that it acts both upstream and downstream of, and even across, genes. The role of the enhancer in the nutritional regulation of rRNA transcription was studied by introducing a centromere plasmid carrying two rRNA minigenes in tandem, flanking a single enhancer, into cells. Analysis of the transcripts from the two minigenes showed that the enhancer was absolutely required for the stimulation of transcription of rRNA that occurs when cells are shifted from a poor carbon source to a good carbon source. While full enhancer function is provided by a 45-bp region at the 3' end of the 190-bp enhancer, some activity was also conferred by other elements, including both a T-rich stretch and a region containing the binding sites for the proteins Reb1p and Abf1p. We conclude that the enhancer is composed of redundant elements and that it is a major element in the regulation of rRNA transcription.

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Year:  1993        PMID: 8423793      PMCID: PMC359013          DOI: 10.1128/mcb.13.2.1283-1289.1993

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  37 in total

1.  Variants of the TATA-binding protein can distinguish subsets of RNA polymerase I, II, and III promoters.

Authors:  M C Schultz; R H Reeder; S Hahn
Journal:  Cell       Date:  1992-05-15       Impact factor: 41.582

2.  Regulation of eukaryotic ribosomal RNA transcription by RNA polymerase modification.

Authors:  E Bateman; M R Paule
Journal:  Cell       Date:  1986-11-07       Impact factor: 41.582

3.  Phosphorylation of the yeast equivalent of ribosomal protein S6 is not essential for growth.

Authors:  C Kruse; S P Johnson; J R Warner
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

4.  Regular distribution of length heterogeneities within non-transcribed spacer regions of cloned and genomic rDNA of Saccharomyces cerevisiae.

Authors:  R Jemtland; E Maehlum; O S Gabrielsen; T B Oyen
Journal:  Nucleic Acids Res       Date:  1986-07-11       Impact factor: 16.971

5.  Effect of growth rate on the amounts of ribosomal and transfer ribonucleic acids in yeast.

Authors:  C Waldron; F Lacroute
Journal:  J Bacteriol       Date:  1975-06       Impact factor: 3.490

6.  Tripartite upstream promoter element essential for expression of Saccharomyces cerevisiae ribosomal protein genes.

Authors:  M O Rotenberg; J L Woolford
Journal:  Mol Cell Biol       Date:  1986-02       Impact factor: 4.272

7.  Naturally occurring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast.

Authors:  K Struhl
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

8.  The major promoter element of rRNA transcription in yeast lies 2 kb upstream.

Authors:  E A Elion; J R Warner
Journal:  Cell       Date:  1984-12       Impact factor: 41.582

9.  Transformation of intact yeast cells treated with alkali cations.

Authors:  H Ito; Y Fukuda; K Murata; A Kimura
Journal:  J Bacteriol       Date:  1983-01       Impact factor: 3.490

10.  3'-End formation of transcripts from the yeast rRNA operon.

Authors:  A E Kempers-Veenstra; J Oliemans; H Offenberg; A F Dekker; P W Piper; R J Planta; J Klootwijk
Journal:  EMBO J       Date:  1986-10       Impact factor: 11.598

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  13 in total

Review 1.  Survey and summary: transcription by RNA polymerases I and III.

Authors:  M R Paule; R J White
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

2.  Identification of a multifunctional domain in autonomously replicating sequence-binding factor 1 required for transcriptional activation, DNA replication, and gene silencing.

Authors:  Tsuyoshi Miyake; Christian M Loch; Rong Li
Journal:  Mol Cell Biol       Date:  2002-01       Impact factor: 4.272

Review 3.  Functional and mechanistic diversity of distal transcription enhancers.

Authors:  Michael Bulger; Mark Groudine
Journal:  Cell       Date:  2011-02-04       Impact factor: 41.582

4.  Molecular cloning and analysis of Schizosaccharomyces pombe Reb1p: sequence-specific recognition of two sites in the far upstream rDNA intergenic spacer.

Authors:  A Zhao; A Guo; Z Liu; L Pape
Journal:  Nucleic Acids Res       Date:  1997-02-15       Impact factor: 16.971

5.  Activated levels of rRNA synthesis in fission yeast are driven by an intergenic rDNA region positioned over 2500 nucleotides upstream of the initiation site.

Authors:  Z Liu; A Zhao; L Chen; L Pape
Journal:  Nucleic Acids Res       Date:  1997-02-01       Impact factor: 16.971

6.  Transcription in the yeast rRNA gene locus: distribution of the active gene copies and chromatin structure of their flanking regulatory sequences.

Authors:  R Dammann; R Lucchini; T Koller; J M Sogo
Journal:  Mol Cell Biol       Date:  1995-10       Impact factor: 4.272

7.  Chromatin structure and transcriptional activity around the replication forks arrested at the 3' end of the yeast rRNA genes.

Authors:  R Lucchini; J M Sogo
Journal:  Mol Cell Biol       Date:  1994-01       Impact factor: 4.272

8.  In vivo binding and hierarchy of assembly of the yeast RNA polymerase I transcription factors.

Authors:  L Bordi; F Cioci; G Camilloni
Journal:  Mol Biol Cell       Date:  2001-03       Impact factor: 4.138

9.  In vitro definition of the yeast RNA polymerase I enhancer.

Authors:  M C Schultz; S Y Choe; R H Reeder
Journal:  Mol Cell Biol       Date:  1993-05       Impact factor: 4.272

10.  Nutritional and growth control of ribosomal protein mRNA and rRNA in Neurospora crassa.

Authors:  T P Cujec; B M Tyler
Journal:  Nucleic Acids Res       Date:  1996-03-01       Impact factor: 16.971

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