Literature DB >> 1461736

The histone mRNA 3' end is required for localization of histone mRNA to polyribosomes.

J Sun1, D R Pilch, W F Marzluff.   

Abstract

The final step in mRNA biosynthesis is transport of the mRNA from the nucleus to the cytoplasm. Histone genes from which the 3' stem-loop has been deleted are transcribed to give RNAs with heterogeneous 3' ends. These RNAs are localized in the nucleus and are stable. Addition of the histone 3' processing signal either on short (< 250 nts) or long (> 1000 nts) transcripts restores 3' processing and transport of the mRNA to the cytoplasm. In addition chimeric histone-U1 snRNA genes which produced RNAs with either histone or U1 3' ends were analyzed. Transcripts which ended with U1 snRNA 3' ends were not efficiently localized to polyribosomes. However, transcripts containing the same sequences including the snRNA 3' end followed by the histone 3' end were present in the cytoplasm on polyribosomes. Taken together these results suggest that the histone 3' end is required for export of histone mRNA to the cytoplasm and association of the mRNA with polyribosomes.

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Year:  1992        PMID: 1461736      PMCID: PMC334473          DOI: 10.1093/nar/20.22.6057

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


  57 in total

1.  3' end formation of U1 snRNA precursors is coupled to transcription from snRNA promoters.

Authors:  H E de Vegvar; E Lund; J E Dahlberg
Journal:  Cell       Date:  1986-10-24       Impact factor: 41.582

2.  The efficiency of 3'-end formation contributes to the relative levels of different histone mRNAs.

Authors:  T J Liu; B J Levine; A I Skoultchi; W F Marzluff
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

3.  Cap trimethylation of U snRNA is cytoplasmic and dependent on U snRNP protein binding.

Authors:  I W Mattaj
Journal:  Cell       Date:  1986-09-12       Impact factor: 41.582

4.  Regulated expression of a chimeric histone gene introduced into mouse fibroblasts.

Authors:  R B Alterman; C Sprecher; R Graves; W F Marzluff; A I Skoultchi
Journal:  Mol Cell Biol       Date:  1985-09       Impact factor: 4.272

5.  Differential expression of two clusters of mouse histone genes.

Authors:  R A Graves; S E Wellman; I M Chiu; W F Marzluff
Journal:  J Mol Biol       Date:  1985-05-25       Impact factor: 5.469

6.  H2A.X. a histone isoprotein with a conserved C-terminal sequence, is encoded by a novel mRNA with both DNA replication type and polyA 3' processing signals.

Authors:  C Mannironi; W M Bonner; C L Hatch
Journal:  Nucleic Acids Res       Date:  1989-11-25       Impact factor: 16.971

7.  Translational control by cytoplasmic polyadenylation during Xenopus oocyte maturation: characterization of cis and trans elements and regulation by cyclin/MPF.

Authors:  L L McGrew; J D Richter
Journal:  EMBO J       Date:  1990-11       Impact factor: 11.598

Review 8.  Poly(A), poly(A) binding protein and the regulation of mRNA stability.

Authors:  P Bernstein; J Ross
Journal:  Trends Biochem Sci       Date:  1989-09       Impact factor: 13.807

9.  Iron regulation of transferrin receptor mRNA levels requires iron-responsive elements and a rapid turnover determinant in the 3' untranslated region of the mRNA.

Authors:  J L Casey; D M Koeller; V C Ramin; R D Klausner; J B Harford
Journal:  EMBO J       Date:  1989-12-01       Impact factor: 11.598

10.  RNA 3' processing regulates histone mRNA levels in a mammalian cell cycle mutant. A processing factor becomes limiting in G1-arrested cells.

Authors:  B Lüscher; D Schümperli
Journal:  EMBO J       Date:  1987-06       Impact factor: 11.598

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  31 in total

1.  Positive and negative mutant selection in the human histone hairpin-binding protein using the yeast three-hybrid system.

Authors:  F Martin; F Michel; D Zenklusen; B Müller; D Schümperli
Journal:  Nucleic Acids Res       Date:  2000-04-01       Impact factor: 16.971

2.  The gene for histone RNA hairpin binding protein is located on human chromosome 4 and encodes a novel type of RNA binding protein.

Authors:  F Martin; A Schaller; S Eglite; D Schümperli; B Müller
Journal:  EMBO J       Date:  1997-02-17       Impact factor: 11.598

3.  Characterization of the 3' untranslated region of the mouse homeobox gene HoxB5.

Authors:  C C Yu; C J Paige; G E Wu
Journal:  Experientia       Date:  1995-06-14

4.  I-PpoI, the endonuclease encoded by the group I intron PpLSU3, is expressed from an RNA polymerase I transcript.

Authors:  J Lin; V M Vogt
Journal:  Mol Cell Biol       Date:  1998-10       Impact factor: 4.272

5.  Two Xenopus proteins that bind the 3' end of histone mRNA: implications for translational control of histone synthesis during oogenesis.

Authors:  Z F Wang; T C Ingledue; Z Dominski; R Sanchez; W F Marzluff
Journal:  Mol Cell Biol       Date:  1999-01       Impact factor: 4.272

6.  The histone 3'-terminal stem-loop is necessary for translation in Chinese hamster ovary cells.

Authors:  D R Gallie; N J Lewis; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1996-05-15       Impact factor: 16.971

7.  Increasing the distance between the snRNA promoter and the 3' box decreases the efficiency of snRNA 3'-end formation.

Authors:  L Ramamurthy; T C Ingledue; D R Pilch; B K Kay; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1996-11-15       Impact factor: 16.971

8.  Human La protein: a stabilizer of histone mRNA.

Authors:  R S McLaren; N Caruccio; J Ross
Journal:  Mol Cell Biol       Date:  1997-06       Impact factor: 4.272

9.  The stem-loop binding protein is required for efficient translation of histone mRNA in vivo and in vitro.

Authors:  Ricardo Sànchez; William F Marzluff
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

10.  Novel 3' ends that support translation.

Authors:  William F Marzluff
Journal:  Genes Dev       Date:  2012-11-15       Impact factor: 11.361

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