Literature DB >> 6432343

The 3' end of drosophila histone H3 mRNA is produced by a processing activity in vitro.

D H Price, C S Parker.   

Abstract

We have examined the process by which the 3' terminus of the Drosophila histone H3 mRNA is produced in vitro. When a template containing a portion of DNA that flanks the normal 3' end of the histone H3 gene and an oligo dC tail on the template strand is transcribed in vitro by Drosophila RNA polymerase II, transcription continues beyond the 3' end of the H3 gene. A processing activity was identified that cleaves the precursor transcript generating an RNA species with the same 3' end as the mature H3 mRNA. The processing activity was partially purified by ion exchange chromatography and sucrose gradient sedimentation. The isolated activity was found to require Mg++ but did not require addition of a nucleoside triphosphate for activity. The activity sedimented with a molecular weight of approximately 140,000 daltons. Transcription of the template and processing of the RNA can be uncoupled in vitro.

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Year:  1984        PMID: 6432343     DOI: 10.1016/0092-8674(84)90497-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  23 in total

1.  Synthesis of U1 RNA in isolated nuclei from sea urchin embryos: U1 RNA is initiated at the first nucleotide of the RNA.

Authors:  G F Morris; W F Marzluff
Journal:  Mol Cell Biol       Date:  1985-05       Impact factor: 4.272

2.  A specific DNA sequence controls termination of transcription in the gastrin gene.

Authors:  K Sato; R Ito; K H Baek; K Agarwal
Journal:  Mol Cell Biol       Date:  1986-04       Impact factor: 4.272

3.  Requirements for accurate and efficient mRNA 3' end cleavage and polyadenylation of a simian virus 40 early pre-RNA in vitro.

Authors:  L C Ryner; J L Manley
Journal:  Mol Cell Biol       Date:  1987-01       Impact factor: 4.272

4.  Tripartite sequences within and 3' to the sea urchin H2A histone gene display properties associated with a transcriptional termination process.

Authors:  M R Johnson; C Norman; M A Reeve; J Scully; N J Proudfoot
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

5.  Molecular localization, developmental expression and nucleotide sequence of the alpha-methyldopa hypersensitive gene of Drosophila.

Authors:  J L Marsh; M P Erfle; C A Leeds
Journal:  Genetics       Date:  1986-10       Impact factor: 4.562

6.  Synthesis of U1 RNA in a DNA-dependent system from sea urchin embryos.

Authors:  G F Morris; D H Price; W F Marzluff
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

7.  Differential expression of individual members of the histone multigene family due to sequences in the 5' and 3' regions of the genes.

Authors:  B J Levine; T J Liu; W F Marzluff; A I Skoultchi
Journal:  Mol Cell Biol       Date:  1988-05       Impact factor: 4.272

8.  Coupling of replication type histone mRNA levels to DNA synthesis requires the stem-loop sequence at the 3' end of the mRNA.

Authors:  B J Levine; N Chodchoy; W F Marzluff; A I Skoultchi
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

9.  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

10.  Cotranscriptional processing of Drosophila histone mRNAs.

Authors:  Todd E Adamson; David H Price
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

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