Literature DB >> 2943587

Genetic complementation in the Xenopus oocyte: co-expression of sea urchin histone and U7 RNAs restores 3' processing of H3 pre-mRNA in the oocyte.

K Strub, M L Birnstiel.   

Abstract

Efficient 3' processing of sea urchin histone H3 pre-mRNA in the Xenopus oocyte is dependent on co-injection of sea urchin U7 RNA or U7 RNP. We show that U7 RNP is a genuine member of the (Sm-type) U-snRNP family as judged by immunoprecipitation of the U7 RNA and U7 RNPs with polyclonal anti-trimethylguanosine and monoclonal anti-Sm antibodies. Sea urchin U7 RNA can be produced in the frog oocyte from RNA genes driven by a Xenopus U2 promoter. The transcripts thus synthesized have all the known characteristics of authentic U7 RNA. Our experiments further suggest that sequences near the 5' end of the U7 RNA mediate Sm-immunoprecipitability. Co-expression of sea urchin U7 RNA gene and H3 histone gene sequences in the frog oocyte complements faulty 3' maturation of histone pre-mRNA. This provides irrefutable evidence that the sea urchin U7 RNA identified earlier is indeed an essential component of the 3' processing of histone mRNAs.

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Year:  1986        PMID: 2943587      PMCID: PMC1166994          DOI: 10.1002/j.1460-2075.1986.tb04411.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  47 in total

1.  Sequences required for 3' end formation of human U2 small nuclear RNA.

Authors:  C Y Yuo; M Ares; A M Weiner
Journal:  Cell       Date:  1985-08       Impact factor: 41.582

2.  Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids.

Authors:  A J Berk; P A Sharp
Journal:  Cell       Date:  1977-11       Impact factor: 41.582

3.  Mapping of RNA by a modification of the Berk-Sharp procedure: the 5' termini of 15 S beta-globin mRNA precursor and mature 10 s beta-globin mRNA have identical map coordinates.

Authors:  R F Weaver; C Weissmann
Journal:  Nucleic Acids Res       Date:  1979-11-10       Impact factor: 16.971

4.  In vivo sequence requirements of the SV40 early promotor region.

Authors:  C Benoist; P Chambon
Journal:  Nature       Date:  1981-03-26       Impact factor: 49.962

5.  Substitutions, insertions, and deletions in two highly conserved U3 RNA species.

Authors:  R Reddy; D Henning; H Busch
Journal:  J Biol Chem       Date:  1980-07-25       Impact factor: 5.157

6.  Identification of regulatory sequences in the prelude sequences of an H2A histone gene by the study of specific deletion mutants in vivo.

Authors:  R Grosschedl; M L Birnstiel
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

7.  A mechanism for RNA splicing.

Authors:  J Rogers; R Wall
Journal:  Proc Natl Acad Sci U S A       Date:  1980-04       Impact factor: 11.205

8.  Spacer DNA sequences upstream of the T-A-T-A-A-A-T-A sequence are essential for promotion of H2A histone gene transcription in vivo.

Authors:  R Grosschedl; M L Birnstiel
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

9.  Are snRNPs involved in splicing?

Authors:  M R Lerner; J A Boyle; S M Mount; S L Wolin; J A Steitz
Journal:  Nature       Date:  1980-01-10       Impact factor: 49.962

10.  Antibodies to small nuclear RNAs complexed with proteins are produced by patients with systemic lupus erythematosus.

Authors:  M R Lerner; J A Steitz
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

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  48 in total

1.  The sea urchin stem-loop-binding protein: a maternally expressed protein that probably functions in expression of multiple classes of histone mRNA.

Authors:  Anthony J Robertson; Jason T Howard; Zbigniew Dominski; Bradley J Schnackenberg; Jan L Sumerel; John J McCarthy; James A Coffman; William F Marzluff
Journal:  Nucleic Acids Res       Date:  2004-02-03       Impact factor: 16.971

2.  Formation of the 3' end of sea urchin U1 small nuclear RNA occurs independently of the conserved 3' box and on transcripts initiated from a histone promoter.

Authors:  B J Wendelburg; W F Marzluff
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

3.  The inability of the Psammechinus miliaris H3 RNA to be processed in the Xenopus oocyte is associated with sequences distinct from those highly conserved amongst sea urchin histone RNAs.

Authors:  F Schaufele; M L Birnstiel
Journal:  Nucleic Acids Res       Date:  1987-10-26       Impact factor: 16.971

Review 4.  Histone 3' ends: essential and regulatory functions.

Authors:  W F Marzluff
Journal:  Gene Expr       Date:  1992

5.  Two promoter elements are necessary and sufficient for expression of the sea urchin U1 snRNA gene.

Authors:  B J Wendelburg; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1992-07-25       Impact factor: 16.971

Review 6.  Formation of the 3' end of histone mRNA: getting closer to the end.

Authors:  Zbigniew Dominski; William F Marzluff
Journal:  Gene       Date:  2007-05-04       Impact factor: 3.688

7.  Characterization of two developmentally regulated sea urchin U2 small nuclear RNA promoters: a common required TATA sequence and independent proximal and distal elements.

Authors:  B Stefanovic; W F Marzluff
Journal:  Mol Cell Biol       Date:  1992-02       Impact factor: 4.272

8.  A conserved region in the sea urchin U1 snRNA promoter interacts with a developmentally regulated factor.

Authors:  K A Stevenson; J C Yu; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

Review 9.  mRNA Editing, Processing and Quality Control in Caenorhabditis elegans.

Authors:  Joshua A Arribere; Hidehito Kuroyanagi; Heather A Hundley
Journal:  Genetics       Date:  2020-07       Impact factor: 4.562

10.  Ribozyme, antisense RNA, and antisense DNA inhibition of U7 small nuclear ribonucleoprotein-mediated histone pre-mRNA processing in vitro.

Authors:  M Cotten; G Schaffner; M L Birnstiel
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

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