Literature DB >> 2139932

Two complex regions, including a TATA sequence, are required for transcription by RNA polymerase I in Neurospora crassa.

B M Tyler1.   

Abstract

In order to define the RNA polymerase I transcriptional apparatus and how it might interact with regulatory signals, the DNA sequences necessary for 40S rRNA transcription in Neurospora crassa were determined. A systematic set of deletion, substitution and insertion mutations were assayed in a homologous in vitro system. The sequences required for transcription of the gene consist of two large domains (I and II) from -113 to -37, and -29 to +4, respectively. Complete deletion of either domain abolished transcription. Upstream sequences confer a small stimulation of transcription. Domain II includes a TATA sequence at -5 which is sensitive to a small (2 bp) substitution and which is conserved among the large rRNA genes of many organisms. Domain I includes a sequence, termed the 'Ribo box', which is also required for transcription of the Neurospora 5S rRNA genes (1), and which occurs in the 5' region of a Neurospora ribosomal protein gene. The 5S and 40S Ribo boxes are shown to be functionally interchangeable.

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Year:  1990        PMID: 2139932      PMCID: PMC330599          DOI: 10.1093/nar/18.7.1805

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


  38 in total

1.  Nucleotide sequence of an RNA polymerase binding site at an early T7 promoter.

Authors:  D Pribnow
Journal:  Proc Natl Acad Sci U S A       Date:  1975-03       Impact factor: 11.205

2.  Regulation of RNA synthesis in Neurospora crassa. An analysis of a shift-up.

Authors:  E Sturani; M G Costantini; R Zippel; F A Alberghina
Journal:  Exp Cell Res       Date:  1976-05       Impact factor: 3.905

3.  Molecular mechanisms governing species-specific transcription of ribosomal RNA.

Authors:  S P Bell; C S Pikaard; R H Reeder; R Tjian
Journal:  Cell       Date:  1989-11-03       Impact factor: 41.582

4.  A rapid alkaline extraction procedure for screening recombinant plasmid DNA.

Authors:  H C Birnboim; J Doly
Journal:  Nucleic Acids Res       Date:  1979-11-24       Impact factor: 16.971

5.  Linker scanner mutagenesis of the Xenopus laevis ribosomal gene promoter.

Authors:  R H Reeder; D Pennock; B McStay; J Roan; E Tolentino; P Walker
Journal:  Nucleic Acids Res       Date:  1987-09-25       Impact factor: 16.971

6.  Inhibition of ribosomal RNA synthesis during a shift-down transition of growth in Neurospora crassa.

Authors:  E Sturani; F Magnani; F A Alberghina
Journal:  Biochim Biophys Acta       Date:  1973-08-24

7.  Deletion mapping of the yeast Pol I promoter.

Authors:  A E Kempers-Veenstra; W Musters; A F Dekker; J Klootwijk; R J Planta
Journal:  Curr Genet       Date:  1985       Impact factor: 3.886

8.  Transcription of Neurospora crassa 5 S rRNA genes requires a TATA box and three internal elements.

Authors:  B M Tyler
Journal:  J Mol Biol       Date:  1987-08-20       Impact factor: 5.469

9.  Mutants affecting amino acid cross-pathway control in Neurospora crassa.

Authors:  I B Barthelmess
Journal:  Genet Res       Date:  1982-04       Impact factor: 1.588

10.  Levels and rates of synthesis of ribosomal ribonucleic acid, transfer ribonucleic acid, and protein in Neurospora crassa in different steady states of growth.

Authors:  F A Alberghina; E Sturani; J R Gohlke
Journal:  J Biol Chem       Date:  1975-06-25       Impact factor: 5.157

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  3 in total

1.  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

2.  A Neurospora crassa ribosomal protein gene, homologous to yeast CRY1, contains sequences potentially coordinating its transcription with rRNA genes.

Authors:  B M Tyler; K Harrison
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

3.  Coordinate expression of ribosomal protein genes in Neurospora crassa and identification of conserved upstream sequences.

Authors:  Y G Shi; B M Tyler
Journal:  Nucleic Acids Res       Date:  1991-12-11       Impact factor: 16.971

  3 in total

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