Literature DB >> 2835659

Functional analysis of the sea urchin U7 small nuclear RNA.

G M Gilmartin1, F Schaufele, G Schaffner, M L Birnstiel.   

Abstract

U7 small nuclear RNA (snRNA) is an essential component of the RNA-processing machinery which generates the 3' end of mature histone mRNA in the sea urchin. The U7 small nuclear ribonucleoprotein particle (snRNP) is classified as a member of the Sm-type U snRNP family by virtue of its recognition by both anti-trimethylguanosine and anti-Sm antibodies. We analyzed the function-structure relationship of the U7 snRNP by mutagenesis experiments. These suggested that the U7 snRNP of the sea urchin is composed of three important domains. The first domain encompasses the 5'-terminal sequences, up to about nucleotides 7, which are accessible to micrococcal nuclease, while the remainder of the RNA is highly protected and hence presumably bound by proteins. This region contains the sequence complementarities between the U7 snRNA and the histone pre-mRNA which have previously been shown to be required for 3' processing (F. Schaufele, G. M. Gilmartin, W. Bannwarth, and M. L. Birnstiel, Nature [London] 323:777-781, 1986). Nucleotides 9 to 20 constitute a second domain which includes sequences for Sm protein binding. The complementarities between the U7 snRNA sequences in this region and the terminal palindrome of the histone mRNA appear to be fortuitous and play only a secondary, if any, role in 3' processing. The third domain is composed of the terminal palindrome of U7 snRNA, the secondary structure of which must be maintained for the U7 snRNP to function, but its sequence can be drastically altered without any observable effect on snRNP assembly or 3' processing.

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Year:  1988        PMID: 2835659      PMCID: PMC363250          DOI: 10.1128/mcb.8.3.1076-1084.1988

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


  44 in total

1.  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

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.  Expression of sea urchin histone genes in the oocyte of Xenopus laevis.

Authors:  E Probst; A Kressmann; M L Birnstiel
Journal:  J Mol Biol       Date:  1979-12-15       Impact factor: 5.469

5.  SnRNAs, SnRNPs, and RNA processing.

Authors:  H Busch; R Reddy; L Rothblum; Y C Choi
Journal:  Annu Rev Biochem       Date:  1982       Impact factor: 23.643

6.  Structural organization of ribonucleoproteins containing small nuclear RNAs from HeLa cells. Proteins interact closely with a similar structural domain of U1, U2, U4 and U5 small nuclear RNAs.

Authors:  J P Liautard; J Sri-Widada; C Brunel; P Jeanteur
Journal:  J Mol Biol       Date:  1982-12-15       Impact factor: 5.469

7.  Intracellular transport of microinjected 5S and small nuclear RNAs.

Authors:  E M De Robertis; S Lienhard; R F Parisot
Journal:  Nature       Date:  1982-02-18       Impact factor: 49.962

8.  Transcriptional fidelity of histone genes injected into Xenopus oocyte nuclei.

Authors:  C Hentschel; E Probst; M L Birnstiel
Journal:  Nature       Date:  1980-11-06       Impact factor: 49.962

9.  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

10.  Biochemical complementation with RNA in the Xenopus oocyte: a small RNA is required for the generation of 3' histone mRNA termini.

Authors:  G Galli; H Hofstetter; H G Stunnenberg; M L Birnstiel
Journal:  Cell       Date:  1983-10       Impact factor: 41.582

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  20 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

Review 2.  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

3.  Evolutionary patterns of non-coding RNAs.

Authors:  Athanasius F Bompfünewerer; Christoph Flamm; Claudia Fried; Guido Fritzsch; Ivo L Hofacker; Jörg Lehmann; Kristin Missal; Axel Mosig; Bettina Müller; Sonja J Prohaska; Bärbel M R Stadler; Peter F Stadler; Andrea Tanzer; Stefan Washietl; Christina Witwer
Journal:  Theory Biosci       Date:  2005-04       Impact factor: 1.919

4.  Unique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processing.

Authors:  Ramesh S Pillai; Matthias Grimmler; Gunter Meister; Cindy L Will; Reinhard Lührmann; Utz Fischer; Daniel Schümperli
Journal:  Genes Dev       Date:  2003-09-15       Impact factor: 11.361

5.  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

6.  Conserved terminal hairpin sequences of histone mRNA precursors are not involved in duplex formation with the U7 RNA but act as a target site for a distinct processing factor.

Authors:  A P Vasserot; F J Schaufele; M L Birnstiel
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

7.  Pre-mRNA topology is important for 3'-end formation in Saccharomyces cerevisiae and mammals.

Authors:  G Stumpf; A Goppelt; H Domdey
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

8.  3' end processing of mouse histone pre-mRNA: evidence for additional base-pairing between U7 snRNA and pre-mRNA.

Authors:  C Spycher; A Streit; B Stefanovic; D Albrecht; T H Koning; D Schümperli
Journal:  Nucleic Acids Res       Date:  1994-10-11       Impact factor: 16.971

9.  Assembly, nuclear import and function of U7 snRNPs studied by microinjection of synthetic U7 RNA into Xenopus oocytes.

Authors:  B Stefanovic; W Hackl; R Lührmann; D Schümperli
Journal:  Nucleic Acids Res       Date:  1995-08-25       Impact factor: 16.971

10.  2'-O-methyl, 2'-O-ethyl oligoribonucleotides and phosphorothioate oligodeoxyribonucleotides as inhibitors of the in vitro U7 snRNP-dependent mRNA processing event.

Authors:  M Cotten; B Oberhauser; H Brunar; A Holzner; G Issakides; C R Noe; G Schaffner; E Wagner; M L Birnstiel
Journal:  Nucleic Acids Res       Date:  1991-05-25       Impact factor: 16.971

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