Literature DB >> 8294511

A 69-kD protein that associates reversibly with the Sm core domain of several spliceosomal snRNP species.

W Hackl1, U Fischer, R Lührmann.   

Abstract

The biogenesis of the spliceosomal small nuclear ribonucleoproteins (snRNPs) U1, U2, U4, and U5 involves: (a) migration of the snRNA molecules from the nucleus to the cytoplasm; (b) assembly of a group of common proteins (Sm proteins) and their binding to a region on the snRNAs called the Sm-binding site; and (c) translocation of the RNP back to the nucleus. A first prerequisite for understanding the assembly pathway and nuclear transport of the snRNPs in more detail is the knowledge of all the snRNP proteins that play essential roles in these processes. We have recently observed a previously undetected 69-kD protein in 12S U1 snRNPs isolated from HeLa nuclear extracts under non-denaturing conditions that is clearly distinct from the U1-70K protein. The following evidence indicates that the 69-kD protein is a common, rather than a U1-specific, protein, possibly associating with the snRNP core particles by protein-protein interaction. (a) Antibodies raised against the 69-kD protein, which did not cross-react with any of the Sm proteins B'-G, precipitated not only U1 snRNPs, but also the other spliceosomal snRNPs U2, U4/U6 and U5, albeit to a lower extent. (b) U1, U2, and U5 core RNP particles reconstituted in vitro contain the 69-kD protein. (c) Xenopus laevis oocytes contain an immunologically related homologue of the human 69-kD protein. When U1 snRNA as well as a mutant U1 snRNA, that can bind the Sm core proteins but lacks the capacity to bind the U1-specific proteins 70K, A, and C, were injected into Xenopus oocytes to allow assembly in vivo, they were recognized by antibodies specific against the 69-kD protein in the ooplasm and in the nucleus. The 69-kD protein is under-represented, if present at all, in purified 17S U2 and in 25S [U4/U6.U5] tri-snRNPs, isolated from HeLa nuclear extracts. Our results are consistent with the working hypothesis that this protein may either play a role in the cytoplasmic assembly of the core domain of the snRNPs and/or in the nuclear transport of the snRNPs. After transport of the snRNPs into the nucleus, it may dissociate from the particles as for example in the case of the 17S U2 or the 25S [U4/U6.U5] tri-snRNP, which bind more than 10 different snRNP specific proteins each in the nucleus.

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Year:  1994        PMID: 8294511      PMCID: PMC2119936          DOI: 10.1083/jcb.124.3.261

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  36 in total

1.  Evidence for three distinct D proteins, which react differentially with anti-Sm autoantibodies, in the cores of the major snRNPs U1, U2, U4/U6 and U5.

Authors:  T Lehmeier; K Foulaki; R Lührmann
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

2.  Immunoaffinity purification of a [U4/U6.U5] tri-snRNP from human cells.

Authors:  S E Behrens; R Lührmann
Journal:  Genes Dev       Date:  1991-08       Impact factor: 11.361

3.  The trimethylguanosine cap structure of U1 snRNA is a component of a bipartite nuclear targeting signal.

Authors:  J Hamm; E Darzynkiewicz; S M Tahara; I W Mattaj
Journal:  Cell       Date:  1990-08-10       Impact factor: 41.582

4.  An essential signaling role for the m3G cap in the transport of U1 snRNP to the nucleus.

Authors:  U Fischer; R Lührmann
Journal:  Science       Date:  1990-08-17       Impact factor: 47.728

Review 5.  Structure of spliceosomal snRNPs and their role in pre-mRNA splicing.

Authors:  R Lührmann; B Kastner; M Bach
Journal:  Biochim Biophys Acta       Date:  1990-11-30

6.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Authors:  H Towbin; T Staehelin; J Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

7.  Structure-probing of U1 snRNPs gradually depleted of the U1-specific proteins A, C and 70k. Evidence that A interacts differentially with developmentally regulated mouse U1 snRNA variants.

Authors:  M Bach; A Krol; R Lührmann
Journal:  Nucleic Acids Res       Date:  1990-02-11       Impact factor: 16.971

8.  Characterisation of human and murine snRNP proteins by two-dimensional gel electrophoresis and phosphopeptide analysis of U1-specific 70K protein variants.

Authors:  A Woppmann; T Patschinsky; P Bringmann; F Godt; R Lührmann
Journal:  Nucleic Acids Res       Date:  1990-08-11       Impact factor: 16.971

9.  Domains of U4 and U6 snRNAs required for snRNP assembly and splicing complementation in Xenopus oocytes.

Authors:  P Vankan; C McGuigan; I W Mattaj
Journal:  EMBO J       Date:  1990-10       Impact factor: 11.598

10.  Nuclear exchange of the U1 and U2 snRNP-specific proteins.

Authors:  R J Feeney; G W Zieve
Journal:  J Cell Biol       Date:  1990-04       Impact factor: 10.539

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  13 in total

1.  Conserved loop I of U5 small nuclear RNA is dispensable for both catalytic steps of pre-mRNA splicing in HeLa nuclear extracts.

Authors:  V Ségault; C L Will; M Polycarpou-Schwarz; I W Mattaj; C Branlant; R Lührmann
Journal:  Mol Cell Biol       Date:  1999-04       Impact factor: 4.272

2.  p54(nrb) associates with the 5' splice site within large transcription/splicing complexes.

Authors:  Sei Kameoka; Paula Duque; Maria M Konarska
Journal:  EMBO J       Date:  2004-04-01       Impact factor: 11.598

3.  In new company: U1 snRNA associates with TAF15.

Authors:  Jennifer F Kugel; James A Goodrich
Journal:  EMBO Rep       Date:  2009-04-17       Impact factor: 8.807

4.  Identification of a human protein that recognizes the 3' splice site during the second step of pre-mRNA splicing.

Authors:  S Wu; M R Green
Journal:  EMBO J       Date:  1997-07-16       Impact factor: 11.598

5.  Transcriptional pulse-chase analysis reveals a role for a novel snRNP-associated protein in the manufacture of spliceosomal snRNPs.

Authors:  S M Noble; C Guthrie
Journal:  EMBO J       Date:  1996-08-15       Impact factor: 11.598

6.  A novel genetic screen for snRNP assembly factors in yeast identifies a conserved protein, Sad1p, also required for pre-mRNA splicing.

Authors:  Z Lygerou; G Christophides; B Séraphin
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

7.  The herpes simplex virus type 1 regulatory protein ICP27 coimmunoprecipitates with anti-Sm antiserum, and the C terminus appears to be required for this interaction.

Authors:  R M Sandri-Goldin; M K Hibbard
Journal:  J Virol       Date:  1996-01       Impact factor: 5.103

8.  Minor intron splicing is regulated by FUS and affected by ALS-associated FUS mutants.

Authors:  Stefan Reber; Jolanda Stettler; Giuseppe Filosa; Martino Colombo; Daniel Jutzi; Silvia C Lenzken; Christoph Schweingruber; Rémy Bruggmann; Angela Bachi; Silvia Ml Barabino; Oliver Mühlemann; Marc-David Ruepp
Journal:  EMBO J       Date:  2016-06-01       Impact factor: 11.598

9.  cDNA cloning of the Sm proteins D2 and D3 from human small nuclear ribonucleoproteins: evidence for a direct D1-D2 interaction.

Authors:  T Lehmeier; V Raker; H Hermann; R Lührmann
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-06       Impact factor: 11.205

10.  snRNP Sm proteins share two evolutionarily conserved sequence motifs which are involved in Sm protein-protein interactions.

Authors:  H Hermann; P Fabrizio; V A Raker; K Foulaki; H Hornig; H Brahms; R Lührmann
Journal:  EMBO J       Date:  1995-05-01       Impact factor: 11.598

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