Specific commitment of different pre-mRNAs to splicing by single SR proteins

No abstract is available for this paper.

• Publication year

  1993

• Venue

  Nature

• Publication date

  1993-09-02

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/365082A0PMID 8361546
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A splicing enhancer complex controls alternative splicing of doublesex pre-mRNA.

  1993cited by this paper
• Distinct functions of SR proteins in alternative pre-mRNA splicing.

  1993cited by this paper
• Protein components specifically associated with prespliceosome and spliceosome complexes.

  1992cited by this paper
• Differential binding of heterogeneous nuclear ribonucleoproteins to mRNA precursors prior to spliceosome assembly in vitro.

  1992cited by this paper
• An ATP-independent U2 small nuclear ribonucleoprotein particle/precursor mRNA complex requires both splice sites and the polypyrimidine tract.

  1992cited by this paper
• The 35-kDa mammalian splicing factor SC35 mediates specific interactions between U1 and U2 small nuclear ribonucleoprotein particles at the 3' splice site.

  1992cited by this paper
• General splicing factors SF2 and SC35 have equivalent activities in vitro, and both affect alternative 5' and 3' splice site selection.

  1992cited by this paper
• SR proteins: a conserved family of pre-mRNA splicing factors.

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• Regulation of alternative pre-mRNA splicing by hnRNP A1 and splicing factor SF2.

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• Isolation of a complementary DNA that encodes the mammalian splicing factor SC35.

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• Two members of a conserved family of nuclear phosphoproteins are involved in pre-mRNA splicing.

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• Associations between distinct pre‐mRNA splicing components and the cell nucleus.

  1991cited by this paper
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• Characterization of cDNAs encoding the polypyrimidine tract-binding protein.

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• An ATP-independent complex commits pre-mRNA to the mammalian spliceosome assembly pathway.

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