Characterization of the Stat5 Protease

• Published in: The Journal of biological chemistry 1999-09, Vol.274 (38), p.26767-26775
• Main Authors: Lee, Carolyn, Piazza, Flavia, Brutsaert, Siska, Valens, Jason, Strehlow, Inga, Jarosinski, Mark, Saris, Chris, Schindler, Christian
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Amino Acid Sequence; Animals; Bone Marrow Cells - cytology; Bone Marrow Cells - enzymology; Cell Differentiation; Cells, Cultured; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Electrophoresis, Polyacrylamide Gel; Endopeptidases - genetics; Endopeptidases - metabolism; HeLa Cells; Humans; Hydrogen-Ion Concentration; Mice; Milk Proteins; Molecular Sequence Data; Molecular Weight; Mutagenesis, Site-Directed; Signal Transduction; STAT5 Transcription Factor; Trans-Activators - genetics; Trans-Activators - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.274.38.26767

Immature myeloid cells have been shown to transduce signals through a carboxyl-terminally truncated isoform of Stat5. This functionally distinct signal transducer and activator of transcription isoform is generated through a unique protein-processing event. Evaluation of numerous cell lines has determined that there is a direct correlation between the expression of truncated Stat5 and protease activity. Moreover, protease activity is found only in the myeloid and not in lymphoid progenitors. To further characterize the protease small quantities have been purified to near homogeneity. Studies on this purified material indicate that the protease has an apparent molecular mass of ∼25 kDa and is active over a wide range of pH values. The protease will also cleave both activated (i.e. tyrosine-phosphorylated) and inactivate Stat5. Although this activity is sensitive to phenylmethylsulfonyl fluoride, it is notably not sensitive to several other serine protease inhibitors. Additional studies have led to the identification of the unique site where the protease cleaves Stat5. Mutagenesis of this site renders Stat5 resistant to cleavage. Consistent with the model that Stat5 cleavage is important for early myeloid development, introduction of a “non-cleavable” isoform of Stat5 into FDC-P1 cells (a myeloid progenitor line) leads to significant phenotypic changes.