Literature DB >> 6093052

Competition between Xenopus satellite I sequences and Pol III genes for stable transcription complex formation.

D L Andrews, L Millstein, B A Hamkalo, J M Gottesfeld.   

Abstract

We have constructed hybrid plasmids bearing both Xenopus 5S RNA genes and satellite I sequences in order to test the effect of satellite DNA on 5S gene transcription. Satellite sequences inactivate 5S transcription in both HeLa S100 and Xenopus oocyte microinjection transcription assays. Inactivation of 5S transcription by satellite DNA is observed both in cis and in trans. Transcription of a tRNA gene is also precluded by satellite I DNA. The Xenopus satellite I repeat contains an RNA polymerase III transcription unit which is highly active in both assay systems. This promoter element is 10- to 25-fold more efficient than the 5S gene in transcription competition assays. This quantitative difference in affinity for transcription components may explain the inactivation of 5S transcription by satellite sequences. The satellite I promoter forms stable transcription complexes in vitro which do not dissociate for at least 30 rounds of transcription. Although stable complex formation on the satellite promoter is largely temperature independent over the range of 0-20 degrees, complex formation on both 5S and tRNA genes exhibits a steep temperature dependence characteristic of DNA helix unwinding. The DNA sequence requirements for stable complex formation on 5S genes have been determined using 5' deletion mutants.

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Year:  1984        PMID: 6093052      PMCID: PMC320198          DOI: 10.1093/nar/12.20.7753

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  19 in total

1.  Transcripts from both strands of a satellite DNA occur on lampbrush chromosome loops of the newt Notophthalmus.

Authors:  M O Diaz; G Barsacchi-Pilone; K A Mahon; J G Gall
Journal:  Cell       Date:  1981-06       Impact factor: 41.582

2.  The activation of RNA synthesis by somatic nuclei injected into amphibian oocytes.

Authors:  L Wakefield; E Ackerman; J B Gurdon
Journal:  Dev Biol       Date:  1983-02       Impact factor: 3.582

3.  Size of the unwound region of DNA in Escherichia coli RNA polymerase and calf thymus RNA polymerase II ternary complexes.

Authors:  H B Gamper; J E Hearst
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1983

Review 4.  Transcription of class III genes: formation of preinitiation complexes.

Authors:  A B Lassar; P L Martin; R G Roeder
Journal:  Science       Date:  1983-11-18       Impact factor: 47.728

5.  Contact points between a positive transcription factor and the Xenopus 5S RNA gene.

Authors:  S Sakonju; D D Brown
Journal:  Cell       Date:  1982-12       Impact factor: 41.582

6.  Stable transcription complex formation of eukaryotic tRNA genes is dependent on a limited separation of the two intragenic control regions.

Authors:  T Dingermann; S Sharp; J Schaack; D Söll
Journal:  J Biol Chem       Date:  1983-09-10       Impact factor: 5.157

7.  Relationship between the two components of the split promoter of eukaryotic tRNA genes.

Authors:  G Ciliberto; C Traboni; R Cortese
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

8.  Stable transcription complexes of Xenopus 5S RNA genes: a means to maintain the differentiated state.

Authors:  D F Bogenhagen; W M Wormington; D D Brown
Journal:  Cell       Date:  1982-02       Impact factor: 41.582

9.  Two conserved sequence blocks within eukaryotic tRNA genes are major promoter elements.

Authors:  G Galli; H Hofstetter; M L Birnstiel
Journal:  Nature       Date:  1981-12-17       Impact factor: 49.962

10.  A quantitative assay for Xenopus 5S RNA gene transcription in vitro.

Authors:  W M Wormington; D F Bogenhagen; E Jordan; D D Brown
Journal:  Cell       Date:  1981-06       Impact factor: 41.582

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  10 in total

1.  Species- and tissue-specific transcription of complex, highly repeated satellite-like Bsp elements in the fox genome.

Authors:  T A Belyaeva; P N Vishnivetsky; V A Potapov; A I Zhelezova; A G Romashchenko
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Differential expression of oocyte-type class III genes with fraction TFIIIC from immature or mature oocytes.

Authors:  W F Reynolds; D L Johnson
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

3.  Sequences preceding the minimal promoter of the Xenopus somatic 5S RNA gene increase binding efficiency for transcription factors.

Authors:  W F Reynolds
Journal:  Nucleic Acids Res       Date:  1989-11-25       Impact factor: 16.971

4.  Small tandemly repeated DNA sequences of higher plants likely originate from a tRNA gene ancestor.

Authors:  A A Benslimane; M Dron; C Hartmann; A Rode
Journal:  Nucleic Acids Res       Date:  1986-10-24       Impact factor: 16.971

5.  Transcriptional activation of Xenopus class III genes in chromatin isolated from sperm and somatic nuclei.

Authors:  A P Wolffe
Journal:  Nucleic Acids Res       Date:  1989-01-25       Impact factor: 16.971

6.  Additional intragenic promoter elements of the Xenopus 5S RNA genes upstream from the TFIIIA-binding site.

Authors:  H J Keller; Q M You; P J Romaniuk; J M Gottesfeld
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

7.  Novobiocin inhibits RNA polymerase III transcription in vitro by a mechanism distinct from DNA topoisomerase II.

Authors:  J M Gottesfeld
Journal:  Nucleic Acids Res       Date:  1986-03-11       Impact factor: 16.971

8.  Transcription of genomic bovine and Xenopus laevis DNA species by RNA polymerase III in HeLa-cell cytosol extracts.

Authors:  J J Furth; C Y Su
Journal:  Biochem J       Date:  1986-08-01       Impact factor: 3.857

9.  The modulatory element TNNCT affects transcription of a Drosophila tRNA(Val)4 gene without affecting transcription complex stability.

Authors:  F G Sajjadi; G B Spiegelman
Journal:  Nucleic Acids Res       Date:  1989-01-25       Impact factor: 16.971

10.  Dominant and specific repression of Xenopus oocyte 5S RNA genes and satellite I DNA by histone H1.

Authors:  A P Wolffe
Journal:  EMBO J       Date:  1989-02       Impact factor: 11.598

  10 in total

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