
We have identified an amino acid sequence in the Drosophila Transformer (Tra) protein that is capable of directing a heterologous protein to nuclear speckles, regions of the nucleus previously shown to contain high concentrations of spliceosomal small nuclear RNAs and splicing factors. This sequence contains a nucleoplasmin-like bipartite nuclear localization signal (NLS) and a repeating arginine/serine (RS) dipeptide sequence adjacent to a short stretch of basic amino acids. Sequence comparisons from a number of other splicing factors that colocalize to nuclear speckles reveal the presence of one or more copies of this motif. We propose a two-step subnuclear localization mechanism for splicing factors. The first step is transport across the nuclear envelope via the nucleoplasmin-like NLS, while the second step is association with components in the speckled domain via the RS dipeptide sequence.
Cell Nucleus, Serine-Arginine Splicing Factors, RNA Splicing, Molecular Sequence Data, Genes, myc, Fluorescent Antibody Technique, Nuclear Proteins, Transfection, Cell Compartmentation, Structure-Activity Relationship, Ribonucleoproteins, Animals, Drosophila Proteins, Humans, Amino Acid Sequence, Cloning, Molecular, Peptides, Cells, Cultured, HeLa Cells
Cell Nucleus, Serine-Arginine Splicing Factors, RNA Splicing, Molecular Sequence Data, Genes, myc, Fluorescent Antibody Technique, Nuclear Proteins, Transfection, Cell Compartmentation, Structure-Activity Relationship, Ribonucleoproteins, Animals, Drosophila Proteins, Humans, Amino Acid Sequence, Cloning, Molecular, Peptides, Cells, Cultured, HeLa Cells
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