Literature DB >> 1692557

A point mutation uncouples RNA 3'-end formation and termination during ribosomal gene transcription in Xenopus laevis.

P Labhart1, R H Reeder.   

Abstract

Two sites, T2 and T3, in the ribosomal gene spacer of Xenopus laevis both direct RNA 3'-end formation 15 bp upstream of the conserved box sequence GACTTGC. Site T2, which defines the 3' end of the 40S precursor, does not terminate transcription whereas site T3 at the 3' end of the spacer does. Here we show that T2 can be converted into a T3-like site with termination activity by a single point mutation 2 bp downstream of the T2 box. RNA 3'-end formation at T2 is unchanged by this mutation. Conversely, a point mutation 2 bp downstream of the T3 box inhibits termination without affecting 3'-end formation. Our results identify two separable events occurring at the 3' end of the ribosomal genes: (1) RNA 3'-end formation by processing and (2) transcription termination. The two processes are directed by two distinct, but overlapping, signals in the DNA sequence. Site T2 in X. laevis is damaged in the second process by a natural mutation.

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Year:  1990        PMID: 1692557     DOI: 10.1101/gad.4.2.269

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  14 in total

1.  Characterization of two types of ribosomal gene transcription in Xenopus laevis oocytes.

Authors:  P Labhart
Journal:  Gene Expr       Date:  1992

2.  The Xenopus 9 bp ribosomal terminator (T3 box) is a pause signal for the RNA polymerase I elongation complex.

Authors:  P Labhart
Journal:  Nucleic Acids Res       Date:  1995-06-25       Impact factor: 16.971

3.  A DNA-binding protein is required for termination of transcription by RNA polymerase I in Xenopus laevis.

Authors:  B McStay; R H Reeder
Journal:  Mol Cell Biol       Date:  1990-06       Impact factor: 4.272

4.  Functional difference between the sites of ribosomal 40S precursor 3' end formation in Xenopus laevis and Xenopus borealis.

Authors:  P Labhart; R H Reeder
Journal:  Nucleic Acids Res       Date:  1990-09-11       Impact factor: 16.971

5.  Plant ribosomal DNA external spacer binding factors: a novel protein binds specifically to a sequence close to the primary pre-rRNA processing site.

Authors:  M Echeverría; P Penon; M Delseny
Journal:  Mol Gen Genet       Date:  1994-05-25

Review 6.  Regulation of ribosomal gene transcription.

Authors:  S T Jacob
Journal:  Biochem J       Date:  1995-03-15       Impact factor: 3.857

7.  Enhancers for RNA polymerase I in mouse ribosomal DNA.

Authors:  C S Pikaard; L K Pape; S L Henderson; K Ryan; M H Paalman; M A Lopata; R H Reeder; B Sollner-Webb
Journal:  Mol Cell Biol       Date:  1990-09       Impact factor: 4.272

8.  DNA-dependent protein kinase specifically represses promoter-directed transcription initiation by RNA polymerase I.

Authors:  P Labhart
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

9.  Different chromatin structures along the spacers flanking active and inactive Xenopus rRNA genes.

Authors:  R Lucchini; J M Sogo
Journal:  Mol Cell Biol       Date:  1992-10       Impact factor: 4.272

10.  The REB1 site is an essential component of a terminator for RNA polymerase I in Saccharomyces cerevisiae.

Authors:  W H Lang; R H Reeder
Journal:  Mol Cell Biol       Date:  1993-01       Impact factor: 4.272

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